| Sr. No. | Title | Date | |
|---|---|---|---|
| 1 |
None Comprehensive analysis of tyrosine kinase domain mutations and imatinib resistance in chronic myeloid leukemia patients
Leuk Res. 2025 Mar 17;152:107679. (IF:2.1)
|
2025 | |
| 2 |
None Protocol for a Multicentric Cohort Study on Neonatal Screening and Early Interventions for Sickle Cell Disease Among High-Prevalence States of India
Diagnostics (Basel). 2025 Mar 14;15(6):730. (IF:3.0)
|
2025 | |
| 3 |
None An Application for Spatial Frailty Models: An Exploration with Data on Fungal Sepsis in Neonates
Diseases. 2025 Mar 14;13(3):83. (IF:2.9)
|
2025 | |
| 4 |
None Predictive Markers for Response to Immunosuppressive Therapy in Aplastic Anaemia
Scand J Immunol. 2025 Mar;101(3):e70010. (IF:4.1)
|
2025 | |
| 5 |
None Alloimmunization Due to Multiple Red Cell Antibodies in a RhD Positive Pregnancy: Lessons to be Learnt
Indian J Hematol Blood Transfus. 2025 Feb 19:1-4. (IF:0.7)
|
2025 | |
| 6 |
None Risk factors of scrub typhus infection in children and adults in Kerala, south India
Asian Pac J Trop Med. 2025 Feb;18(2):84-92. (IF:1.9)
|
2025 | |
| 7 |
None Temporal Trends of Dog Bite Cases and their Correlation with Meteorological Factors in a Metropolitan City
Indian J Community Med. 2025 Feb;:10-4103. (IF:0.9)
|
2025 | |
| 8 |
None Identification of a GFI1B variant associated with abnormal platelet function and normal platelet count
Br J Haematol. 2025 Feb;206(2):777-780.
|
2025 | |
| 9 |
None Coincidental occurrence of severe factor XII deficiency in a case of mild hemophilia A: a unique coagulation laboratory diagnostic conundrum
Blood Coagul Fibrinolysis. 2025 Jan 27. doi: 10.1097/MBC.0000000000001346.
|
2025 | |
| 10 |
None Variant Klinefelter Syndrome With Xq Trisomy (47,X,i(X)(q10),Y): A Case Report and Review of the Literature
Cureus. 2025 Jan 12;17(1):e77351. (IF:1.2)
|
2025 | |
| 11 |
None Weak or partial D: Importance of molecular characterization of D variants
Transfus Apher Sci. 2025 Jan 11;64(2):104069. (IF:1.4)
|
2025 | |
| 12 |
None Occurrence of "under-the-radar" antibiotic resistance in anthropogenically affected produce
ISME J. 2025 Jan 2;19(1):wrae261. (IF:10.8)
|
2025 | |
| 13 |
None Hematopoietic Stem Cell Transplant of a Congenital Dyserythropoietic Anemia Type II Patient: A Rare Report from the Indian Population
Indian J Hematol Blood Transfus. 2025 Jan;41(1):194-196. (IF:0.7)
|
2025 | |
| 14 |
None Assessing and managing iron deficiency anemia in sickle cell disease: Insights from a systematic review and meta-analysis
J Postgrad Med. 2025 Jan–Mar;71(1):33-40.
|
2025 | |
| 15 |
None Mutational Landscape of Patients with Wiskott Aldrich Syndrome: Update from India
J Clin Immunol. 2024 Dec 17;45(1):56. (IF:7.2)
|
2024 | |
| 16 |
None Yoga-based lifestyle intervention for healthy ageing in older adults: a two-armed, waitlist randomized controlled trial with multiple primary outcomes
Geroscience. 2024 Dec;46(6):6039-6054. (IF:5.3)
|
2024 | |
| 17 |
None Whispers of the Genome: Unmasking SNP through Simple Modified PCR
Indian Journal of Anthropological Research. 2024 Dec;3(2):291-303.
|
2024 | |
| 18 |
None Rare red cell enzymopathies in the Indian population: A comprehensive review
Pediatric Hematology Oncology Journal. 2024 Dec;9(4):235-243.
|
2024 | |
| 19 |
None Unveiling Immunological Signatures and Predictors of Response to Immunosuppressive Therapy in Acquired Aplastic Anaemia
Clin Exp Immunol. 2024 Nov 12;218(3):291-299. (IF:3.4)
|
2024 | |
| 20 |
None Duffy Binding Protein Ligand (PvDBP) gene duplication in Indian P. Vivax Malaria isolates: implication for malaria research
Curr Genet. 2024 Nov 9;70(1):18. (IF:1.8)
|
2024 | |
| 21 |
None PLCG2-associated immune dysregulation (PLAID) comprises broad and distinct clinical presentations related to functional classes of genetic variants
J Allergy Clin Immunol. 2024 Jan;153(1):230-242. (IF:14.29)
|
2024 | |
| 22 |
None Autoimmune anti‐D in an RhD‐positive young infant: Learning from a rare case.
Vox Sanguinis. 2024 Jan;119(1):70-3. Short Report (IF:1.8)
|
2024 | |
| 23 |
None Cleavage-resistant RIPK1-induced autoinflammatory syndrome-A report of three generations with periodic fever and clinical response to colchicine.
Int J Rheum Dis. 2024 Jan;27(1):e14837.(IF:2.4)
|
2024 | |
| 24 |
None Prevalence of Oral Potentially Malignant Lesions, Tobacco use, and Effect of Cessation Strategies among Solid Waste Management workers in Northern India: a pre-post intervention study
BMC Oral Health. 2024 Oct 26;24(1):1292. (IF:2.6)
|
2024 | |
| 25 |
None Microbiome in sickle cell disease: Pathophysiology and therapeutic insights
Br J Haematol. 2024 Oct;205(4):1279-1287. (IF:5.1)
|
2024 | |
| 26 |
None Immunophenotypic Analysis of Patients with Pyogenic Liver Abscess for Underlying Inborn Errors of Immunity
Indian J Pediatr. 2024 Oct;91(10):1105. (IF:2.1)
|
2024 | |
| 27 |
None Non-syndromic congenital sideroblastic anaemia; phenotype, and genotype of 15 Indian patients
Ann Hematol. 2024 Oct;103(10):3987-3998. (IF:3.0)
|
2024 | |
| 28 |
None ACKR1 gene polymorphisms in Bombay blood group (O(h)) individuals of Indian origin
Transfus Apher Sci. 2024 Oct;63(5):103975. (IF:1.4)
|
2024 | |
| 29 |
None Silver hair in a neonate: a tale of 2 fatal cases
Oxf Med Case Reports. 2024;2024(9):omae106. (IF:N/A)
|
2024 | |
| 30 |
None Major Histocompatibility Complex (MHC) Class II Deficiency- A Case of Primary Immunodeficiency Disorder
Indian J Pediatr. 2024 Sep;91(9):967-969. (IF:2.1)
|
2024 | |
| 31 |
None Unveiling Immunological Signatures and Predictors of Response to Immunosuppressive Therapy in Acquired Aplastic Anaemia
Clin Exp Immunol. 2024 Aug 13:uxae076. (IF:3.4)
|
2024 | |
| 32 |
None Fibrosis and Hepatocarcinogenesis: Role of Gene-Environment Interactions in Liver Disease Progression
Int J Mol Sci. 2024 Aug 8;25(16):8641. (IF:4.9)
|
2024 | |
| 33 |
None Efficacy of daily versus intermittent oral iron supplementation for prevention of anaemia among pregnant women: a systematic review and meta-analysis
EClinicalMedicine. 2024 Jul 17;74:102742. (IF:9.9)
|
2024 | |
| 34 |
None Immunodeficiency-Related Vaccine-Derived Poliovirus (iVDPV) Excretion in an Infant with Severe Combined Immune Deficiency with Spillover to a Parent
Vaccines (Basel). 2024 Jul 9;12(7):759. (IF:7.8)
|
2024 | |
| 35 |
None Preconceptional paternal caloric restriction of high-fat diet-induced obesity in Wistar rats dysregulates the metabolism of their offspring via AMPK/SIRT1 pathway
Lipids Health Dis. 2024 Jun 8;23(1):174. (IF:3.9)
|
2024 | |
| 36 |
None Double Trouble: Novel Digenic CD19-RABEP2 Deletion in Predominantly Antibody Deficiency with Syndromic Features.
J Clin Immunol. 2024 Jun 7;44(6):144. (IF:7.2)
|
2024 | |
| 37 |
None Clinical Utility of Flow-Cytometry for Diagnosis and Genotype Phenotype Correlation in a Cohort of X-linked Agammaglobulinemia Patients.
Indian J Pediatr. 2024 Jun;91(6):638. (IF:4.3)
|
2024 | |
| 38 |
None Wide spectrum of novel and rare hemoglobin variants in the multi-ethnic Indian population: A review.
Int J Lab Hematol. 2024 Jun;46(3):434-450. (IF:2.2)
|
2024 | |
| 39 |
None Sickle cell disease in India: current status and progress.
Lancet Haematol. 2024 May;11(5):e322-e323. (IF:15.4)
|
2024 | |
| 40 |
None Low-dose Emicizumab prophylaxis in severe haemophilia A patients -a retrospective study bringing new hope for our patients.
J Thromb Haemost. 2024 Apr;22(4):1024-1030. (IF:16.041)
|
2024 | |
| 41 |
None Cancer pattern in Varanasi district from Uttar Pradesh state of India, a foundation for cancer control based on the first report of the population-based cancer registry.
Indian J Cancer. 2024 Apr 1;61(2):383-389. (IF:1.0)
|
2024 | |
| 42 |
None Exploring factors influencing the perspective regarding HIV transmission and prevention among college students in India.
J Family Med Prim Care. 2024 Apr;13(4):1467-1472. (IF:1.1)
|
2024 | |
| 43 |
None Knowledge and perceptions about clinical research and its ethical conduct among college students from non-science background: a representative nation-wide survey from India.
BMJ Public Health 2024;2:e000748.
|
2024 | |
| 44 |
None Profile and geospatial analysis of dog bite cases attending the antirabies vaccine outpatient department at the tertiary level hospital of Mumbai.
Indian J Public Health. 2024 Apr 1;68(2):175-179. (IF:0.9)
|
2024 | |
| 45 |
None Interplay of missed opportunity for vaccination and poor response to the vaccine led to measles outbreak in a slum area of Eastern Mumbai, India.
Epidemiol Infect. 2024 Mar 18;152:e56. (IF:2.5)
|
2024 | |
| 46 |
None Impact of climate change on temperature variations and extrinsic incubation period of malaria parasites in Chennai, India- Implications on its disease transmission potential.
Parasites Vectors. 2024 Mar 15;17(1):134.(IF:4.0)
|
2024 | |
| 47 |
None Comprehensive study of chromosomal CNVs and genomic variations predicting overall survival in Myelodysplastic syndromes.
Oncology. 2024 Mar;102(10):897-906. (IF:3.5)
|
2024 | |
| 48 |
None Diagnosis and Management of Infections in Patients with Mendelian Susceptibility to Mycobacterial Disease.
Pathogens. 2024 Feb 25;13(3):203.(IF:3.3)
|
2024 | |
| 49 |
None Role of hydroxyurea therapy in the prevention of organ damage in sickle cell disease: a systematic review and meta-analysis.
Syst Rev. 2024 Feb 8;13(1):60. Systematic Review & Meta Analysis (IF:6.3)
|
2024 | |
| 50 |
None Efficacy of combined HBsAg, anti-HBc and anti-HBs screening in minimizing transfusion transmission risk of hepatitis B infection in low resource setting.
Heliyon. 2024 Feb 3;10(3):e25805 (IF:3.4)
|
2024 | |
| 51 |
None When a synonymous mutation breaks the silence in a thalassaemia patient.
Br J Haematol. 2024 Feb;204(2):677-682. (IF:5.1)
|
2024 | |
| 52 |
None HNF1 Associated Novel Missense Mutation Associated with MODY-3 and Type 2 Diabetes in an Indian Family
Am J Biomed Sci & Res. Nov 2023: 19(2) AJBSR.MS.ID.002574, DOI: 10.34297 AJBSR.2023.19.002574 (Impact factor: 1.628).
|
2023 | |
| 53 |
None A Clinical Conundrum with Diagnostic and Therapeutic Challenge: a Tale of Two Disorders in One Case.
J Clin Immunol. 2023 Nov;43(8):1891-1902. (IF:8.542)
|
2023 | |
| 54 |
None Challenges in screening for sickle cell disease among newborns from the tribal region of Palghar, Maharashtra during the COVID-19 pandemic.
Indian J Med Res. 2023 Oct 1;158(4):378-383. (IF:5.274)
|
2023 | |
| 55 |
None Satellite Epidemic of Covid-19 Associated Mucormycosis in India: A Multi-Site Observational Study.
Mycopathologia 2023 Oct;188(5):745-753.(IF:3.785)
|
2023 | |
| 56 |
None Editorial: NK cell defects: diagnosis and treatment.
Front Immunol. 2023 Oct 31;14:1323793. doi: 10.3389/fimmu.2023.1323793. eCollection 2023.(IF:8.787)
|
2023 | |
| 57 |
None Genomic and computational analysis of four novel variants of MPL gene in Congenital Amegakaryocytic Thrombocytopenia.
Ann Hematol. 2023 Oct;102(10):2683-2693.(IF:3.5)
|
2023 | |
| 58 |
None Fibrosis and bone marrow: understanding causation and pathobiology
J Transl Med. 2023 Oct 9;21(1):703.(IF:8.448)
|
2023 | |
| 59 |
None Monogenic inborn errors of immunity in autoimmune disorders
Immunol Res. 2023 Oct;71(5):771-780. (IF:4.4)
|
2023 | |
| 60 |
None Congenital Dyserythropoietic Anemia Type II: High Prevalence of c.1385A>G, (p.Tyr462Cys) Mutation in the Indian Population.
Indian J Pediatr. 2023 Aug;90(8):840. (IF:1.136)
|
2023 | |
| 61 |
None Normative data for paediatric lymphocyte subsets: A pilot study from western India.
Indian J Med Res. 2023 Aug;158(2):161-174. (IF:5.274)
|
2023 | |
| 62 |
None Exploring risk factors and transmission dynamics of Hepatitis B infection among Indian families: Implications and perspective.
J Infect Public Health. 2023 Jul;16(7):1109-1114. (IF:7.537)
|
2023 | |
| 63 |
None Development of High-Resolution Melting Curve Analysis for rapid detection of SEC23B gene mutation causing Congenital Dyserythropoietic Anemia type II in Indian population.
Ital J Pediatr. 2023 Jul 16;49(1):84.(IF:3.288)
|
2023 | |
| 64 |
None Assessment of Enterovirus Excretion and Identification of VDPVs in Patients with Primary Immunodeficiency in India: Outcome of ICMR-WHO Collaborative Study Phase-I.
Vaccines (Basel). 2023 Jul 6;11(7):1211. (IF:7.8)
|
2023 | |
| 65 |
None Effect of hydroxyurea on erythrocyte apoptosis in hemoglobinopathy patients.
Expert Rev Hematol.2023 Jul-Dec;16(9):685-692. doi: 10.1080/17474086.2023.2231152. (IF: 2.8)
|
2023 | |
| 66 |
None Clinical, immunological and molecular findings of patients with DOCK-8 deficiency from India
Scand J Immunol. 2023 Jul;98(1):e13276. .(IF:3.889)
|
2023 | |
| 67 |
None Expanding the clinical phenotype of FADD deficiency with a novel mutation and its role in Fas-mediated apoptotic pathway.
Br J Haematol. 2023 Jul;202(2):e11-e15.(IF:8.615)
|
2023 | |
| 68 |
None A comparative study of modulatory interaction between cytokines and apoptotic proteins among Scleroderma patients with and without pulmonary involvement.
Cytokine 2023 Jun;166:156183.(IF:3.926)
|
2023 | |
| 69 |
None Synergetic effect of Azacitidine and Sorafenib in treatment of a case of myeloid neoplasm with sole chromosomal abnormality t(8;22)(p11.2;q11.2)/BCR-FGFR1 rearrangement
Cancer Genet. 2023 Jun;274-275:26-29. (IF:2.169)
|
2023 | |
| 70 |
None Evaluating the Efficacy of Certain Intermediate Irrigants in Preventing Precipitate Formed Due to Sodium Hypochlorite and Chlorhexidine Within the Root Canal System: An In Vitro Study.
Cureus 2023 Jun 2;15(6):e39871.(IF:1.2)
|
2023 | |
| 71 |
None Targeted next-generation sequencing identifies eighteen novel mutations expanding the molecular and clinical spectrum of PKLR gene disorders in the Indian population
Ann Hematol. 2023 May;102(5):1029-1036.(IF:4.03)
|
2023 | |
| 72 |
None Poliovirus surveillance in patients with primary immunodeficiencies, India
Bull World Health Organ. 2023 May 1;101(5):346-354.(IF:11.1)
|
2023 | |
| 73 |
None Higher proinflammatory responses possibly contributing to suppressed cytotoxicity in patients with COVID-19 associated mucormycosis
Immunobiology. 2023 May;228(3):152384.(IF:3.152)
|
2023 | |
| 74 |
None Response of stem cells derived from human exfoliated deciduous teeth to Bio-C Repair and Mineral Trioxide Aggregate Repair HP: Cytotoxicity and gene expression assessment.
Dent Res J (Isfahan). 2023 Apr 26;20:55. eCollection 2023.(IF:1.23)
|
2023 | |
| 75 |
None Vitamin D receptor genetic polymorphisms in severe and recurrent tuberculosis in children
Indian J Tuberc. 2023 Apr;70(2):239-244.(IF:1.57)
|
2023 | |
| 76 |
None Overview of the serologic and molecular basis of D variants with a focus on D variants in the Indian population
Immunohematology. 2023 Apr 5;39(1):19-31.(IF:0.268)
|
2023 | |
| 77 |
None Hematologically important mutations: Leukocyte adhesion deficiency (second update)
Blood Cells Mol Dis. 2023 Mar;99:102726.(IF:2.3)
|
2023 | |
| 78 |
None Clinical features, laboratory and molecular findings of children with leukocyte adhesion deficiency type-III from a single center in India.
Pediatric Hematology Oncology Journal Volume 8, Issue 1, March 2023, Pages 4-9 (IF : 1.969)
|
2023 | |
| 79 |
None Targeted next-generation sequencing identifies novel deleterious variants in ANK1 gene causing severe hereditary spherocytosis in Indian patients: expanding the molecular and clinical spectrum
Mol Genet Genomics. 2023 Mar;298(2):427-439.(IF:3.1)
|
2023 | |
| 80 |
None pH-responsive microparticles of rifampicin for augmented intramacrophage uptake and enhanced antitubercular efficacy.
Int J Pharm. 2023 Mar 25;635:122729.(IF:5.8)
|
2023 | |
| 81 |
None Perturbations of immune landscape in COVID-19 associated mucormycosis. M
Mycoses. 2023 Mar;66(3):226-236.(IF:4.9)
|
2023 | |
| 82 |
None Dynamic interplay of microRNA in diseases and therapeutic A.
Clin Genet. 2023 Mar;103(3):268-276. (IF:3.5)
|
2023 | |
| 83 |
None Changing outcomes of stem cell transplantation in primary immunodeficiencies: Results from a tertiary-care charitable trust hospital in Mumbai.
J Allergy Clin Immunol Glob. 2023 Mar 29;2(3):100105. (IF: --)
|
2023 | |
| 84 |
None SPENCD Presenting with Evans Phenotype and Clinical Response to JAK1/2 Inhibitors-a Report of 2 Cases.
J Clin Immunol. 2023 Feb;43(2):331-334.(IF:9.1)
|
2023 | |
| 85 |
None Chronic Hepatitis B and Related Liver Diseases Are Associated with Reduced 25-Hydroxy-Vitamin D Levels: A Systematic Review and Meta-Analysis.
Biomedicines. 2023 Jan 5;11(1):135. doi: 10.3390/biomedicines11010135. PMID: 36672644; PMCID: PMC9855868. (IF:4.7)
|
2023 | |
| 86 |
None Over expression of mTOR gene predicts overall survival in myelodysplastic syndromes
Mol Biol Rep. 2023 Jan;50(1):235-244. (IF:2.8)
|
2023 | |
| 87 |
None Comprehensive molecular analysis identifies eight novel variants in XY females with disorders of sex development.
Mol Hum Reprod. 2023 Jan 31;29(2):gaad001.(IF:4.0)
|
2023 | |
| 88 |
None Impact of COVID-19 infection among indian sickle cell disease patients.A.
Indian J Public Health. 2023 Jan-Mar;67(1):112-116.(IF:1.7)
|
2023 | |
| 89 |
None Frequency and pattern of chromosomal abnormalities in acute myeloid leukemia from Western India: A retrospective study
J Cancer Res Ther. 2023 Jan-Mar;19(2):340-346.(IF:1.3)
|
2023 | |
| 90 |
None Role of microRNA in hydroxyurea mediated HbF induction in sickle cell anaemia patients.
Sci Rep. 2023 Jan 7;13(1):369. (IF:3.8)
|
2023 | |
| 91 |
None Hemoglobin Reims- a rare alphgaglobin chain varinay and its interaction with beta thalassemia
Journal of Hematopathology. Received: 21 June 2022 / Accepted: 31 August 2022 doi.org/10.1007/s12308-022-00512-9 (IF :0.196)
|
2022 | |
| 92 |
None A case control investigation of Covid-19 associated mucormycosis in India.
BMC Infect Dis. 2022 Nov 16;22(1):856. (IF: 3.714)
|
2022 | |
| 93 |
None Utility of HLA-DR in screening panel for errors of immunity.
Scandinavian Journal of Immunology. Published online 2022 Nov. https://doi.org/10.1111/sji.13238 (IF: 3.7)
|
2022 | |
| 94 |
None Comparative study of clinical features and vaccination status in Omicron and non-Omicron infected patients during the third wave in Mumbai, India.
J Family Med Prim Care. 2022 Oct;11(10):6135-6142. doi: 10.4103/jfmpc.jfmpc_430_22. Epub 2022 Oct 31. PMID: 36618147; PMCID: PMC9810849. (IF: 0.57)
|
2022 | |
| 95 |
None Dynamic interplay of microRNA in diseases and therapeutic.
Clinical Genetics. 2022 Oct 30. http://doi.org/10.1111/cge.14256 (IF: 5.422)
|
2022 | |
| 96 |
None Role of Oxidative Stress and the Protective Effect of Fermented Papaya Preparation in Sickle Cell Disease.
Hemoglobin. 2022 Sep 8:1-5. doi: 10.1080/03630269.2022.2118603. Online ahead of print. (IF: 0.849)
|
2022 | |
| 97 |
None Co- inheritance of Hb Ottawa and HbS: a rare interaction leading to an interesting diagnostic challenge
Journal of Hematopathology. https://doi.org/10.1007/s12308-022-00514-7. Received: 15 July 2022 / Accepted: 6 September 2022 (IF:0.196)
|
2022 | |
| 98 |
None A systematic review on hydroxyurea therapy for sickle cell disease in India.
Indian J Med Res. 2022 Aug;156(2):299-311. doi: 10.4103/ijmr.ijmr_3447_21. PMID: 36629190. .(IF: 5.274)
|
2022 | |
| 99 |
None Targeted next-generation sequencing revealed a novel homozygous mutation in the LRBA gene causes severe haemolysis associated with Inborn Errors of Immunity in an Indian family
Hematology. 2022 Dec;27(1):441-448. doi: 10.1080/16078454.2022.2058736. (IF :2.269)
|
2022 | |
| 100 |
None XMEN saved by magnesium.
Immunol. 2022 May;95(5):e13154. doi: 10.1111/sji.13154. Epub 2022 Mar 9. (IF:3.487)
|
2022 | |
| 101 |
None Novel RASGRP2 variants in platelet function defects: Indian study
Br J Haematol. 2022 May;197(3):377-380 (IF 6.998)
|
2022 | |
| 102 |
None A Cross Sectional Assessment of the Profile of Risk Factors of Non-Communicable Diseases Among Health Care Staff of a Tertiary Cancer Hospital.
Lifestyle Med. 2022 May 31;12(2):98-103. doi: 10.15280/jlm.2022.12.2.98. PMID: 36157886; PMCID: PMC9490011. .(IF: 1.85)
|
2022 | |
| 103 |
None Antibody profile in post- vaccinated & SARS-CoV-2-infected individuals.
Indian J Med Res. 2022 May-Jun;155(5&6):538-545. (IF: 5.274)
|
2022 | |
| 104 |
None SLGT2 Inhibitor Rescues Myelopoiesis in G6PC3 Deficiency
J Clin Immunol. 2022 Jul 15. doi: 10.1007/s10875-022-01323-4. Online ahead of print. (IF 8.317)
|
2022 | |
| 105 |
None Diagnostic challenges posed by a rare unstable hemoglobin variant Hb Southampton HBB c.320T C with pyrimidine 5 nucleotidase deficiency and the response to HU therapy
Blood Cells Mol Dis. 2022 May 7;96:102667. doi:10.1016/j.bcmd.2022.102667. Online ahead of print (IF :3.039)
|
2022 | |
| 106 |
None Comprehensive analysis of genetic factors predicting overall survival in Myelodysplastic syndromes
Sci Rep. 2022 Apr 8;12(1):5925. doi: 10.1038/s41598-022-09864-9. (IF 4.379)
|
2022 | |
| 107 |
None STAT 3 GOF with Polycythemia: a Twist to the Tale-First Case Report from India.
J Clin Immunol. 2022 May;42(4):866-868 (IF:8.317)
|
2022 | |
| 108 |
None Clinical, immunological and genomic characteristics of children with X-linked agammaglobulinemia from Kerala, South India
Hum Immunol. 2022 Apr;83(4):335-345. doi: 10.1016/j.humimm.2022.01.003. Epub 2022 Jan 21 (IF:2.85)
|
2022 | |
| 109 |
None Gastrointestinal involvement ofcommon variable immunodeficiency: A diagnostic challenge to the physician.
J R Coll Physicians Edinb. 2022 Mar;52(1):34-38. doi: 10.1177/14782715221088963. PMID: 36146961 (IF 0.726)
|
2022 | |
| 110 |
None Three novel mutations in CYB5R3 gene causing NADH-cytochrome b5 reductase enzyme deficiency leads to recessive congenital methaemoglobinemia.
Mol Biol Rep. 2022 Mar;49(3):2141-2147 (IF: 2.316 )
|
2022 | |
| 111 |
None Clinical and Genetic Spectrum of Inborn Errors of Immunity in a Tertiary Care Center in Southern India.
Indian J Pediatr. 2022 Mar;89(3):233-242 (IF:1.967)
|
2022 | |
| 112 |
None Rapid molecular identification of a rare β-globin gene deletion & its clinical implication.
Indian J Med Res. 2022 Mar;155(3&4):432-437.(IF:2.267)
|
2022 | |
| 113 |
None Vanishing Lymphocytes in a Case of Vanishing Bone Disease
J Clin Immunol. 2022 Apr 42(3): 706-708. (IF:8.317)
|
2022 | |
| 114 |
None XMEN saved by magnesium.
Scand J Immunol. 2022 Mar 9:e13154. doi: 10.1111/sji.13154. Online ahead of print.(IF : 3.487)
|
2022 | |
| 115 |
None Algorithm development and diagnostic accuracy testing for non-invasive foetal RHD genotyping: an Indian experience.
Blood Transfus. 2022 May;20(3):235-244. doi: 10.2450/2021.0022-21. Epub 2021 Mar 31. (IF: 3.443)
|
2022 | |
| 116 |
None Newborn Screening for Sickle Cell Disease Among Tribal Populations in the States of Gujarat and Madhya Pradesh in India: Evaluation and Outcome Over 6 Years.
Front Med (Lausanne)2022 Feb 15;8:731884. (IF :5.091)
|
2022 | |
| 117 |
None Novel RASGRP2 variants in platelet function defects: Indian study
Br J Haematol. 2022 Feb;197(3):377-380 (IF 6.998)
|
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None Impact of functional IL-18 polymorphisms on genetic predisposition and diverse clinical manifestations of the disease in Indian SLE patients.
Lupus. 2019 Apr;28(4):545-554
|
2019 | |
| 237 |
None A Novel G6PD p. Gly 321 Val Mutation Causing Severe Hemolysis in an Indian Infant.
Indian J Hematol Blood Transfus. 2019 Apr;35(2):399-401.
|
2019 | |
| 238 |
None Chromosomal Aberrations in Primary Amenorrhea: A Retrospective Study.
J Hum Reprod Sci. 2019 Apr-Jun;12(2):92-97.
|
2019 | |
| 239 |
None Diagnostic challenges posed by a rare alpha globin chain variant Hb Fontainebleau in a pregnant female and its potential effects in her children in view of multiple globin gene defects in her husband.
Indian J Pathol Microbiol. 2019 Apr-Jun;62(2):323-325.
|
2019 | |
| 240 |
None The phenotypic and molecular diversity of hemoglobinopathies in India: A review of 15 years at a referral center.
Int J Lab Hematol. 2019 Apr;41(2):218-226. (IF:1.919)
|
2019 | |
| 241 |
None Red Cell Distribution Width (RDW): Normative Data in Indian Neonates.
J Pediatr Hematol Oncol. 2019 Mar;41(2): e119-e-121.(IF: 1.060)
|
2019 | |
| 242 |
None Lymphopenia and Severe Combined Immunodeficiency (SCID) - Think Before You Ink.
Indian J Pediatr. 2019 Mar 16.doi:10.1007/s12098-019-02904-9.[Epub ahead of print] (IF: 1.046 )
|
2019 | |
| 243 |
None Novel Deleterious Sequence Change in the NLRP12 Gene in a Child with the Autoinflammatory Syndrome, Joint Hypermobility and Cutis Laxa from India.
Mediterr J Hematol Infect Dis. 2019 Mar 1;11(1):e2019018.
|
2019 | |
| 244 |
None A novel DKC1 gene mutation c.1177 A>T (p.I393F) in a case of dyskeratosis congenita with severe telomere shortening.
Int J Dermatol. 2019 Mar 13. doi: 10.1111/ijd.14424. [Epub ahead of print]
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2019 | |
| 245 |
None Natural Killer Cell Degranulation Defect: A Cause for Impaired NK-Cell Cytotoxicity a and Hyperinflammation in Fanconi Anemia Patients.
Front Immunol. 2019 Mar 21;10:490. eCollection 2019 (IF: 3.35)
|
2019 | |
| 246 |
None Anti-factor VIII inhibitors against A2 and C2 domains in hemophilia A patients from India.
Blood Cells Mol Dis. 2018 Mar;75:11-12.(IF:1.836)
|
2019 | |
| 247 |
None Clinical, Immunological, and Molecular Findings in 57 Patients With Severe Combined Immunodeficiency (SCID) From India.
Front Immunol. 2019 Feb 4;10:23. eCollection 2019. (IF: 5.511)
|
2019 | |
| 248 |
None IFN-g:IL-10 Ratio: a Putative Predictive Biomarker to Discriminate HLH From Severe Viral Infections.
J Clin Immunol. 2019 Feb;39(2):135-137. (IF: 4.227)
|
2019 | |
| 249 |
None Partial trisomy 9 (9pter->9q22.1) and partial monosomy 14 (14pter- >14q11.2) due to paternal translocation t(9;14)(q22.1;q11.2) in a case of Dysmorphic features.
Intractable Rare Dis Res. 2019 Feb;8(1):72-77
|
2019 | |
| 250 |
None Role of polymorphisms in MMP-9 and TIMP-1 as biomarkers for susceptibility to systemic lupus erythematosus patients.
Biomark Med. 2019 Jan; 13(1):33-43.(IF:2.346)
|
2019 | |
| 251 |
None Molecular diagnosis of unexplained haemolytic anaemia using targeted next-generation sequencing panel revealed (p.Ala337Thr) novel mutation in GPI gene in two Indian patients.
J Clin Pathol. 2019 Jan;72(1):81-85.(IF:2.894)
|
2019 | |
| 252 |
None Red Cell Indices and Hemoglobin Profile of Newborn Babies with Both the Sickle Gene and Alpha Thalassaemia in Central India.
Indian J Hematol Blood Transfus. 2019 Jan;35(1):109-113. (IF: 0.474)
|
2019 | |
| 253 |
None Differential role of Kruppel like factor 1 (KLF1) gene in red blood cell disorders.
Genomics. 2018 Dec 5. pii: S0888-7543(18)30542-1. doi: 10.1016/j.ygeno.2018.11.032.[Epub ahead of print] (IF: 2.910)
|
2018 | |
| 254 |
None Genetic lesions in the UGT1A1 genes among Gilberts syndrome patients from India.
Mol Biol Rep. 2018 Dec; 45(6):2733-2739.(IF:1.889)
|
2018 | |
| 255 |
None Molecular genotyping of clinically important blood group antigens in patients with thalassaemia.
Indian J Med Res. 2018 Dec;148(6):713-720. (IF: 1.508)
|
2018 | |
| 256 |
None The spatial epidemiology of sickle-cell anaemia in India.
Sci Rep. 2018 Dec 6;8(1):17685.(IF:4.122)
|
2018 | |
| 257 |
None Role of lupus anticoagulants in immediate acting inhibitor positivity in congenital haemophilia A patients.
Thromb Res. 2018 Dec;172:29-35.(IF:2.779)
|
2018 | |
| 258 |
None Differentially expressed serum host proteins in hepatitis B and C viral infections.
Virusdisease. 2018 Dec;29(4):468-477.(IF:0.364)
|
2018 | |
| 259 |
None A study of prevalence of autoantibodies in patients with lichen planus from Mumbai, India.
Indian J Dermatol Venereol Leprol. 2018 Nov-Dec;84(6):667-671.(IF: 2.229)
|
2018 | |
| 260 |
None Approach to Molecular Diagnosis of Chronic Granulomatous Disease (CGD): an Experience from a Large Cohort of 90 Indian Patients.
J Clin Immunol. 2018 Nov;38(8):898-916. (IF: 4.227)
|
2018 | |
| 261 |
None Adipokine interactions promote the pathogenesis of systemic lupus erythematosus.
Cytokine. 2018 Nov;111:20-27 (IF:3.514)
|
2018 | |
| 262 |
None Rare ?- and ?-Globin Gene Mutations in the Pathare Prabhus: Original Inhabitants of Mumbai, India.
Hemoglobin. 2018 Sep - Nov;42(5-6):297-301. (IF: 0.462)
|
2018 | |
| 263 |
None Effect of Assorted Globin Haplotypes and ?-Thalassemia on the Clinical Heterogeneity of Hb S-?-Thalassemia.
Hemoglobin. 2018 Nov 29:1-7.(IF:0.462)
|
2018 | |
| 264 |
None Prevalence and Association of Dermatological Manifestations with Fanconi Anemia: A Retrospective Study.
Indian Dermatol Online J. 2018 Sep-Oct;9(5):341-342.(IF: --)
|
2018 | |
| 265 |
None Hereditary elliptocytosis: A rare red cell membrane disorder.
Indian J Hematol Blood Transfus 2018 Oct;34(4):754-755.(IF:0.474)
|
2018 | |
| 266 |
None Imatinib resistance due to a novel and rare class of mutation at position S348 (1043nt C?A) of Bcr/Abl gene in a chronic myeloid leukemia patient.
Leuk Res. 2018 Sep;72:96-98.(IF:2.319)
|
2018 | |
| 267 |
None Catalytic antibodies in patients with systemic lupus erythematosus.
Eur J Rheumatol. 2018 Sep;5(3):173-178. (IF: --)
|
2018 | |
| 268 |
None Novel mutation (R192C) in CYB5R3 gene causing NADH-cytochrome b5 reductase deficiency in eight Indian patients associated with autosomal recessive congenital methemoglobinemia type-I.
Hematology. 2018 Sep;23(8):567-573.(IF: 1.315)
|
2018 | |
| 269 |
None p47phox-/- Chronic Granulomatous Disease Patient with Incomplete Kawasaki Disease.
J Clin Immunol. 2018 Aug;38(6):638-641.(IF:4.227)
|
2018 | |
| 270 |
None Potential involvement of ubiquitin-proteasome system dysfunction associated with oxidative stress in the pathogenesis of sickle cell disease.
Br J Haematol. 2018 Aug;182(4):559-566. (IF: 5.128)
|
2018 | |
| 271 |
None Innate immune gene polymorphisms and their association with neonatal sepsis.
Infect Genet Evol. 2018 Aug;62:205-210.(IF:2.545)
|
2018 | |
| 272 |
None Prenatal Diagnosis of HbE-?-Thalassemia: Experience of a Center in Western India.
Indian J Hematol Blood Transfus. 2018 Jul;34(3):474-479 (IF:0.474)
|
2018 | |
| 273 |
None Hepatitis C virus infection in a tertiary care hospital in Mumbai, India: Identification of a mixed and novel genotype.
Indian J Med Microbiol. 2018 Jul-Sep;36(3):352-356.(IF: 1.157)
|
2018 | |
| 274 |
None First Observation of Hb Lepore Hollandia in the Baiga Tribal Family.
Indian J Hematol Blood Transfus. 2018 Jul;34(3):581-584.(IF:0.474)
|
2018 | |
| 275 |
None A retrospective study of quality management system at National Reference Laboratory in Mumbai- highlighting quality in HIV testing.
International J Med Sci Public Health 2018 June; 7(10):1-6. Online First (IF:)
|
2018 | |
| 276 |
None Clinical, Immunological, and Molecular Findings in Four Cases of B Cell Expansion With NF-?B and T Cell Anergy Disease for the First Time From India.
Front Immunol. 2018 Jun 14;9:1049. eCollection 2018. (IF: 3.35)
|
2018 | |
| 277 |
None A novel p.Pro353His SERPINC1 mutation in the thrombin-binding region affecting stability of Antithrombin molecule in an extended Omani family.
Int J Lab Hematol. 2018 Jun;40(3):e49-e51. (IF: 1.919)
|
2018 | |
| 278 |
None Two Novel C-Terminal Frame shift Mutations in the CYB5R3 Gene Lead to Global Growth and Methemoglobinemia Type II. Developmental Delay associated with Recessive Congenital
Journal of Medical Science and Clinical Research 2018 June;6(6):626-636.(IF:6.379)
|
2018 | |
| 279 |
None Molecular basis of weak D expression in the Indian population and report of a novel, predominant variant RHD allele.
Transfusion. 2018 Jun;58(6):1540-1549. (IF: 3.423)
|
2018 | |
| 280 |
None Molecular genotyping of Indian blood group system antigens in Indian blood donors.
Transfus Apher Sci. 2018 Jun;57(3):388-390. (IF: --)
|
2018 | |
| 281 |
None Microparticles as prognostic biomarkers in dengue virus infection.
Acta Trop. 2018 May;181:21-24. (IF: 2.509)
|
2018 | |
| 282 |
None RHD-Positive Alleles among D- C/E+ Individuals from India.
Transfus Med Hemother. 2018 May;45(3):173-177. (IF: 2.152)
|
2018 | |
| 283 |
None Association of clinical and serological parameters of systemic lupus erythematosus patients with Epstein-Barr virus antibody profile.
J Med Virol. 2018 Mar;90(3):559-563.(IF: 1.988)
|
2018 | |
| 284 |
None Multiple Heritable and Acquired Risk Factors in a Case of Recurrent Retinal Vein Occlusion.
J Assoc Physicians India. 2018 Mar;66(3):76-78.(IF:0.37)
|
2018 | |
| 285 |
None Warfarin Dose Model for the Prediction of Stable Maintenance Dose in Indian Patients.
Clin Appl Thromb Hemost. 2018 Mar;24(2):353-359.(IF: 2.096)
|
2018 | |
| 286 |
None Heterogeneity of O blood group in India: Peeping through the window of molecular biology.
Asian J Transfus Sci. 2018 Jan-Jun;12(1):62-68. (IF: --)
|
2018 | |
| 287 |
None A possible need for routine screening for Strongyloides stercoralis infection in Indian haemophilia patients.
Indian J Med Res. 2018 Mar;147(3):315-317 (IF: 1.508)
|
2018 | |
| 288 |
None Screening for DEL phenotype in RhD negative Indians.
J Clin Lab Anal. 2018 Mar;32(3). doi: 10.1002/jcla.22288. Epub 2017 Jun 23 (IF:1.303)
|
2018 | |
| 289 |
None Clinical, Immunological, and Molecular Findings in Five Patients with Major Histocompatibility Complex Class II Deficiency from India.
Front Immunol. 2018 Feb 16;9:188.(IF: 5.511)
|
2018 | |
| 290 |
None Plasmodium falciparum malaria skews globin gene expression balance in in-vitro haematopoietic stem cell culture system: Its implications in malaria associated anemia.
Exp Parasitol. 2018 Feb;185:29-38.(IF: 1.821)
|
2018 | |
| 291 |
None Heterogeneity of O blood group in India: Peeping through the window of molecular biology.
Asian J Transfus Sci. 2018 Jan-Jun;12(1):62-68. (IF: 1.06)
|
2018 | |
| 292 |
None Newborn Screening for Hemoglobinopathies and Red Cell Enzymopathies in Tripura State: A Malaria-Endemic State in Northeast India.
Hemoglobin. 2018 Jan;42(1):43-46. (IF: 0.67)
|
2018 | |
| 293 |
None Red cell distribution width and its association with mortality in neonatal sepsis.
J Matern Fetal Neonatal Med. 2018 Jan 8:1-6.(IF: 1.493)
|
2018 | |
| 294 |
None Predisposition of IL-1? (-511 C/T) polymorphism to renal and hematologic disorders in Indian SLE patients.
Gene 2018 Jan 30;641:41-45.(IF: 3.191)
|
2018 | |
| 295 |
None Circulating microfilariae in haematological malignancies: do they have a role in pathogenesis?
J Helminthol. 2018 Jan;92(1):125-127.(IF: 1.61)
|
2018 | |
| 296 |
None Microparticles as prognostic biomarkers in dengue virus infection.
Acta Trop. 2018 Jan 31;181:21-24.(IF: 2.509)
|
2018 | |
| 297 |
None Effect of inherited red cell defects on growth of Plasmodium falciparum: An in vitro study.
Indian J Med Res. 2018 Jan;147(1):102-109.(IF: 1.508)
|
2018 | |
| 298 |
None Congenital dyserythropoietic anemia type II mimicking hereditary spherocytosis in Indian patient with SEC23B-Y462C mutations.
Ann Hematol. 2017 Dec;96(12):2135-2139. (IF: 3.083)
|
2017 | |
| 299 |
None Phenotypic Prenatal Diagnosis of Chronic Granulomatous Disease: A Useful Tool in The Absence Of Molecular Diagnosis.
Scand J Immunol. 2017 Dec;86(6):486-490. (IF: 2.314)
|
2017 | |
| 300 |
None Glucose phosphate isomerase (GPI) Tadikonda: Characterization of a novel Pro340Ser mutation.
Pediatr Hematol Oncol. 2017 Dec 11:1-6. (IF: 1.12)
|
2017 | |
| 301 |
None A novel homozygous frameshift mutation in Exon 7 of the ADAMTS13 gene in a patient with congenital thrombotic thrombocytopenic purpura from India: a case report.
Transfusion. 2017 Nov;57(11):2712-2714. (IF: 3.386)
|
2017 | |
| 302 |
None Asialoglycoprotein receptor targeted delivery of doxorubicin nanoparticles for hepatocellular carcinoma.
Drug Deliv. 2017 Nov;24(1):20-29(IF: 6.402)
|
2017 | |
| 303 |
None Poliovirus Excretion in Children with Primary Immunodeficiency Disorders, India.
Emerg Infect Dis. 2017 Oct;23(10):1664-1670. (IF: 8.222)
|
2017 | |
| 304 |
None Combination of copeptin, placental growth factor and total annexin V microparticles for prediction of preeclampsia at 10-14 weeks of gestation.
Placenta. 2017 Oct;58:67-73. (IF: 2.759)
|
2017 | |
| 305 |
None Somatic mosaicism in a severe haemophilia B family detected by allele specific PCR: An alert to the genetic diagnostic laboratories.
Thromb Res. 2017 Oct;158:138-139. (IF: 2.65)
|
2017 | |
| 306 |
None Synergistic effect of two ??globin gene cluster mutations leading to the hereditary persistence of fetal hemoglobin (HPFH) phenotype.
Mol Biol Rep 2017 Oct;44(5):413-417. (IF: 1.828)
|
2017 | |
| 307 |
None A de novo factor VIII mutation in a haemophilia B family leading to combined deficiency of factor VIII and IX.
Haemophilia. 2017 Sep;23(5):e477-e479. (IF: 3.569)
|
2017 | |
| 308 |
None Evolution of technology for molecular genotyping in blood group systems.
Indian J Med Res. 2017 Sep;146(3):305-315.(IF:1.532)
|
2017 | |
| 309 |
None Next-generation sequencing: emerging technology in the area of hematology and blood disorder.
Hematol Blood Disord 2017 Sep;1(1):1-2. (IF: )
|
2017 | |
| 310 |
None Investigation of Plasminogen Activator Inhibitor-1 (PAI-1) 4G/5G promoter polymorphism in Indian venous thrombosis patients: A case-control study.
Eur J Haematol. 2017 Sep; 99(3):249-254. (IF: 2.653)
|
2017 | |
| 311 |
None Role of MMP-7 in the pathogenesis of systemic lupus erythematosus (SLE).
Lupus. 2017 Aug;26(9):937-943. (IF: 2.454)
|
2017 | |
| 312 |
None Mortality caused by intracranial bleeding in non-severe hemophilia A patients: comment.
J Thromb Haemost. 2017 Aug; 15(8):1709-10. (IF: 5.287)
|
2017 | |
| 313 |
None A functional SNP MCP-1 (-2518A/G) predispose to renal disorder in Indian Systemic Lupus Erythematosus patients.
Cytokine. 2017 Aug;96:189-194. (IF: 3.488)
|
2017 | |
| 314 |
None Dosing algorithms for vitamin K antagonists across VKORC1 and CYP2C9 genotypes: comment.
J Thromb Haemost. 2017 Aug; 15(8):1708. (IF: 5.287)
|
2017 | |
| 315 |
None First report of Rhnull individuals in the Indian population and characterization of the underlying molecular mechanisms.
Transfusion. 2017 Aug;57(8):1944-1948 (IF: 3.386)
|
2017 | |
| 316 |
None Association of Heme Oxygenase-1 (Number of GT Repeats) with the methemoglobin levels in recessive congenital methemoglobinemia in Indian population.
J Molecular Genet Medicine 2017 Jul; 11(3):1-5 (IF: 2.20)
|
2017 | |
| 317 |
None Does novel P5N-1 mutation in combination with G6PD Asahi in an Indian male contribute to Budd Chiari Syndrome?
Blood Cells Mol Dis. 2017 Jul;66:8-10. (IF: 1.882)
|
2017 | |
| 318 |
None Dysfunctional fibrinolysis and cerebral venous thrombosis.
Blood Cells Mol Dis. 2017 Jun;65:51-55. (IF: 1.882)
|
2017 | |
| 319 |
None Low T cell receptor excision circles (TRECs) in a case of ZAP 70 deficient severe combined immunodeficiency (SCID) with a novel mutation from India.
Blood Cells Mol Dis. 2017 Jun;65:95-96. (IF: 1.882)
|
2017 | |
| 320 |
None Does the Novel KLF1 Gene Mutation Lead to a Delay in Fetal Hemoglobin Switch?
Ann Hum Genet. 2017 May;81(3):125-128. (IF: 1.659)
|
2017 | |
| 321 |
None A microplate reader-based method to quantify NADH-cytochrome b5 reductase activity for diagnosis of recessive congenital methaemoglobinemia.
Hematology. 2017 May;22(4):252-257 (IF: )
|
2017 | |
| 322 |
None Effect of the Hemochromatosis Mutations on Iron Overload among the Indian ? Thalassemia Carriers.
J Clin Lab Anal. 2017 May;31(3).(IF: 1.521)
|
2017 | |
| 323 |
None Do high sensitivity C-reactive protein and serum interleukin-6 levels correlate with disease activity in systemic lupus erythematosuspatients?
J Postgrad Med. 2017 Apr-Jun;63(2):92-95. (IF: 0.912)
|
2017 | |
| 324 |
None Lead poisoning induced severe hemolytic anemia, basophilic stippling, mimicking erythrocyte pyrimidine 5’-nucleotidase deficiency in Beta thalassemia minor.
J Clin Toxicol 2017 Apr; 7(2):1-3. (IF: 3.677)
|
2017 | |
| 325 |
None Identification of high oxygen affinity hemoglobin (Hb Andrew-Minneapolis) in an Indian family.
|
2017 | |
| 326 |
None Centrosome Aberration Frequency and Disease Association in B-Acute Lymphoblastic Leukemia.
In Vivo. 2017 Mar-Apr;31(2):215-220. (IF: 0.953)
|
2017 | |
| 327 |
None Identification of a novel S184F mutation causing glucose-6-phosphate-dehydrogenase deficiency in a tribal family of Madhya Pradesh, India.
Meta Gene, 2017 Mar; 12:130-133. (IF: 1.27)
|
2017 | |
| 328 |
None A Comparitive Study of Anticardiolipin Antibodies among Systemic Lupus Erythematosus Patients from Western and Eastern India.
J Assoc Physicians India. 2017 Mar;65(3):14-19. (IF: 0.37)
|
2017 | |
| 329 |
None Predominant Neurologic Manifestations Seen in a Patient With a Biallelic Perforin1 Mutation (PRF1; p.R225W).
J Pediatr Hematol Oncol. 2017 Mar;39(2):143-146. (IF: 1.076)
|
2017 | |
| 330 |
None Impact of TNF-? and LT? gene polymorphisms on genetic susceptibility in Indian SLE patients.
Hum Immunol. 2017 Feb;78(2):201-208. (IF: 2.311)
|
2017 | |
| 331 |
None Characterization of two novel FANCG mutations in Indian Fanconi anemia patients.
Leuk Res. 2017 Feb;53:50-56. (IF: 2.501)
|
2017 | |
| 332 |
None Mutations in linker for activation of T cells (LAT) lead to a novel form of severe combined immunodeficiency.
J Allergy Clin Immunol. 2017 Feb;139(2):634-642.e5. (IF: 13.081)
|
2017 | |
| 333 |
None Synergistic effect of factor VII gene polymorphisms causing mild factor VII deficiency in a case of severe factor X deficiency.
Blood Coagul Fibrinolysis. 2017 Jan;28(1):105-106.(IF: 1.367)
|
2017 | |
| 334 |
None A novel mutation in GP1BA gene leads to mono-allelic Bernard Soulier syndrome form of macrothrombocytopenia.
Blood Coagul Fibrinolysis. 2017 Jan;28(1):94-95.(IF: 1.367)
|
2017 | |
| 335 |
None Management of pregnancy in dysfibrinogenemia cases: a dilemma.
Blood Coagul Fibrinolysis. 2017 Jan;28(1):91-93. (IF: 1.367)
|
2017 | |
| 336 |
None Genetic Variations in Bilirubin Metabolism Genes and Their Association with Unconjugated Hyperbilirubinemia in Adults.
Ann Hum Genet. 2017 Jan;81(1):11-19.(IF: 1.659)
|
2017 | |
| 337 |
None Phenotypic expression of HbO Indonesia in two Indian families and its interaction with sickle hemoglobin.
Indian J Pathol Microbiol. 2017 Jan-Mar;60(1):79-83.(IF: 0.616)
|
2017 | |
| 338 |
None Do b-globin gene variants contribute in substantial reduction in HbA2 levels?
Int. J. Lab Hematol 2016 Dec;38(6):610-615.(IF: 2.03)
|
2016 | |
| 339 |
None Betrixaban in Acutely Ill Medical Patients.
N Engl J Med. 2016 Dec 15;375(24):e50.(IF: 72.406)
|
2016 | |
| 340 |
None Clinical, Immunological, and Molecular Findings of Patients with p47phox Defect Chronic Granulomatous Disease (CGD) in Indian Families.
J Clin Immunol. 2016 Nov;36(8):774-784. (IF: 3.253)
|
2016 | |
| 341 |
None Clinical and molecular epidemiology of factor XI deficiency in India.
Thromb Res. 2016 Nov;147:85-87.(IF: 2.65)
|
2016 | |
| 342 |
None Cell signaling in putative leukemic stem cells and blast population in acute myeloid leukemia.
Leuk Lymphoma. 2016 Sep;57(9):2195-8. (IF: 2.755)
|
2016 | |
| 343 |
None Management of Haemophilia in Developing Countries: Challenges and Options.
Indian J Hematol Blood Transfus. 2016 Sep;32(3):347-55.(IF: 0.403)
|
2016 | |
| 344 |
None Bengal macrothrombocytopenia is not totally an innocuous condition.
Blood Cells Mol Dis. 2016 Sep;60:3-6.(IF: 1.882)
|
2016 | |
| 345 |
None First trimester prenatal diagnosis of severe FXIII deficiency.
Haemophilia. 2016 Sep;22(5):e443-4. (IF: 3.569)
|
2016 | |
| 346 |
None Hb E-?-Thalassemia in Five Indian States.
Hemoglobin. 2016 Sep;40(5):310-315.(IF: 0.77)
|
2016 | |
| 347 |
None Antigen negative red blood cell inventory of Indian blood donors.
Transfus Apher Sci. 2016 Aug;55(1):131-5. (IF: 1.3)
|
2016 | |
| 348 |
None Adenosine Deaminase Deficiency with a Novel Gene Mutation.
Indian J Pediatr. 2016 Aug;83(8):875-6. (IF: 0.945)
|
2016 | |
| 349 |
None Cytogenetic abnormalities and genomic copy number variations in EPO (7q22) and SEC-61(7p11) genes in primary myelodysplastic syndromes.
Blood Cells Mol Dis. 2016 Jul;59:52-7.(IF: 1.882)
|
2016 | |
| 350 |
None Congenital macrothrombocytopenia is a heterogeneous disorder in India.
Haemophilia. 2016 Jul; 2(4):570-82.(IF: 3.569)
|
2016 | |
| 351 |
None Pleiotropic Roles of Metalloproteinases in Hematological Malignancies: an Update.
Asian Pacific J. of Cancer Prevention 2016 Jul; 17(7):3043-51.(IF: 2.39)
|
2016 | |
| 352 |
None A common missense variant in exon 5 of antithrombin gene (SERPINC1) in Indian patients with thrombosis.
Thromb Res. 2016 Jul;143:1-2.(IF: 2.65)
|
2016 | |
| 353 |
None Comment on Salomon et al. Gestational Diabetes Mellitus Is Associated With Changes in the Concentration and Bioactivity of Placenta-Derived Exosomes in Maternal Circulation Across Gestation. Diabetes 2016;65:598-609.
Diabetes. 2016 Jul;65(7):e24-5.(IF: 8.684)
|
2016 | |
| 354 |
None Can hydroxyurea serve as a free radical scavenger and reduce iron overload in ?-thalassemia patients?
Free Radic Res. 2016 Jul; 27:1-7.(IF: 3.188)
|
2016 | |
| 355 |
None Does HbF induction by hydroxycarbamide work through MIR210 in sickle cell anaemia patients?
Br J Haematol. 2016 Jun;173(5):801-3. (IF: 5.67)
|
2016 | |
| 356 |
None Five Rare ? Globin Chain Hemoglobin Variants in India.
Indian J Hematol Blood Transfus. 2016 Jun;32(Suppl 1):282-6.(IF: 0.403
|
2016 | |
| 357 |
None Could procoagulant cell-derived microparticles have a more crucial role in pregnancy complications rather than exosomes?
Am J Obstet Gynecol. 2016 Jun;214(6):765-6. (IF: 5.574)
|
2016 | |
| 358 |
None Partial matching of blood group antigens to reduce alloimmunization in Western India.
Transfus Apher Sci. 2016 Jun;54(3):390-5.(IF: 1.3)
|
2016 | |
| 359 |
None A Modified NK Cell Degranulation Assay Applicable for Routine Evaluation of NK Cell Function.
J Immunol Res. 2016;2016:3769590.(IF: 4.856)
|
2016 | |
| 360 |
None Influence of single nucleotide polymorphisms in the BCL11A and HBS1L-MYB gene on the HbF levels and clinical severity of sickle cell anaemia patients.
Ann Hematol. 2016 Jun;95(7):1201-3.(IF: 3.083)
|
2016 | |
| 361 |
None Noninvasive fetal RHD genotyping from maternal plasma
Global Journal of Transfusion Science 2016 Jan-Jun;1(1): 21-28.(IF:--)
|
2016 | |
| 362 |
None Indian Bombay phenotype: it is different!
Blood Transfus. 2016 Jun 24;15(1):74-76. (IF: 1.607)
|
2016 | |
| 363 |
None Correlation between 'H' blood group antigen and Plasmodium falciparum invasion.
Ann Hematol. 2016 Jun;95(7):1067-75.(IF: 3.083)
|
2016 | |
| 364 |
None Annexin A5 levels or circulating microparticles: what we see depends mainly on what we look for.
J Intern Med. 2016 Jun;279(6):608. (IF: 7.598)
|
2016 | |
| 365 |
None Current Updates on Classification, Diagnosis and Treatment of Hemophagocytic Lymphohistiocytosis (HLH).
Indian J Pediatr. 2016 May;83(5):434-43.(IF: 0.945)
|
2016 | |
| 366 |
None Application of Flow Cytometry in the Evaluation of Primary Immunodeficiencies.
Indian J Pediatr. 2016 May;83(5):444-9.(IF: 0.945)
|
2016 | |
| 367 |
None Possible selection of host folate pathway gene polymorphisms in patients with malaria from a malaria endemic region in North East India.
Trans R Soc Trop Med Hyg. 2016 May;110(5):294-8.(IF: --)
|
2016 | |
| 368 |
None Why should hemophilia B be milder than hemophilia A?
Haematologica. 2016 May;101(5):e213. (IF: 7.702)
|
2016 | |
| 369 |
None Preeclampsia: simplified or still miles to go?
Am J Obstet Gynecol. 2016 May;214(5):668-9.(IF: 5.574)
|
2016 | |
| 370 |
None Hemoglobinopathy Screening by Osmotic Fragility Test Based on Flow Cytometer or Naked Eye.
Cytometry B Clin Cytom. 2016 May;90(3):279-84.(IF: 2.474)
|
2016 | |
| 371 |
None Association of Serum Ferritin Levels with Hematological Manifestations in Systemic Lupus Erythematosus Patients from Western India.
J Assoc Physicians India. 2016 May;64(5):14-18.(IF: 0.37)
|
2016 | |
| 372 |
None Factor VIII Antigen, Activity, and Mutations in Hemophilia A.
Clin Appl Thromb Hemost. 2016 May;2(4):381-5.(IF: 2.096)
|
2016 | |
| 373 |
None Antigen expression on a putative leukemic stem cell population and AML blast.
Int J Hematol. 2016 May;103(5):567-71.(IF: 1.61)
|
2016 | |
| 374 |
None Guidelines for Screening, Early Diagnosis and Management of Severe Combined Immunodeficiency (SCID) in India.
Indian J Pediatr. 2016 May;83(5):455-62 (IF: 0.945)
|
2016 | |
| 375 |
None Re: Does low-molecular-weight heparin influence fetal growth or uterine and umbilical arterial Doppler in women with a history of early-onset uteroplacental insufficiency and an inheritable thrombophilia? Secondary randomised controlled trial results LMWH
BJOG. 2016 Apr;123(5):844.(IF: 5.051)
|
2016 | |
| 376 |
None A triad of telomerase, androgen receptor and early growth response 1 in prostate cancer cells.
Cancer Biol Ther. 2016 Apr 2;1(4):439-48.(IF: 3.294)
|
2016 | |
| 377 |
None A simple clot based assay for detection of procoagulant cell-derived microparticles.
Clin Chem Lab Med. 2016 Apr 1;54(5):799-803.(IF: 3.432)
|
2016 | |
| 378 |
None F8 gene mutation profile in Indian hemophilia A patients: Identification of 23 novel mutations and factor VIII inhibitor risk association.
Mutat Res. 2016 Apr;786:27-33.(IF: 5.5)
|
2016 | |
| 379 |
None Genetic basis of severe factor XIII deficiency in a large cohort of Indian patients: Identification of fourteen novel mutations.
Blood Cells Mol Dis. 2016 Mar;57:81-4.(IF: 1.882)
|
2016 | |
| 380 |
None Does consumption of platelet-derived microparticles in the fibrin clot explain the decrease in their percentage during pregnancy?
Blood Cells Mol Dis. 2016 Mar;57:115-7.(IF: 1.882)
|
2016 | |
| 381 |
None Epidemiology of hepatocellular carcinoma (HCC) in hemophilia.
Crit Rev Oncol Hematol. 2016 Mar;99:129-33.(IF: 4.971)
|
2016 | |
| 382 |
None Prediction of small-for-gestational-age at 35-37 weeks of gestation: too late for management?
Ultrasound Obstet Gynecol. 2016 Mar;47(3):385.(IF: 4.71)
|
2016 | |
| 383 |
None Differential antigen expression and aberrant signaling via PI3/AKT, MAP/ERK, JAK/STAT, and Wnt/? catenin pathways in Lin-/CD38-/CD34+ cells in acute myeloid leukemia.
Eur J Haematol. 2016 Mar;96(3):309-17.(IF: 2.653)
|
2016 | |
| 384 |
None Secretion and Expression of Matrix Metalloproteinase-2 and 9 from Bone Marrow Mononuclear Cells in Myelodysplastic Syndrome and Acute Myeloid Leukemia.
Asian Pac J Cancer Prev. 2016 Mar;17(3):1519-29.(IF: 2.39 )
|
2016 | |
| 385 |
None Analysis of Complement Recepter Type I(CR1) Polymorphisms and Its Association with Malaria in Rural Population of Maharashtra.
World J Res Review. 2016 Mar;2(3):13-17.(IF: )
|
2016 | |
| 386 |
None Decrease in circulating percentage platelet microparticles during pregnancy-a different perspective.
Ann Hematol. 2016 Feb;95(3):533-4.(IF: 3.083)
|
2016 | |
| 387 |
None Erythropoiesis in Malaria Infections and Factors Modifying the Erythropoietic Response.
Anemia. 2016;2016:9310905. Epub 2016 Feb 29. Review. (IF: 3.00)
|
2016 | |
| 388 |
None Neonatal Screening and the Clinical Outcome in Children with Sickle Cell Disease in Central India.
PLoS One. 2016 Jan 19;11(1):e0147081.(IF: 2.806)
|
2016 | |
| 389 |
None FANCA Gene Mutations with 8 Novel Molecular Changes in Indian Fanconi Anemia Patients.
PLoS One. 2016 Jan 22;11(1):e0147016.(IF: 2.806)
|
2016 | |
| 390 |
None Use of lectins in immunohematology.
Asian J Transfus Sci. 2016 Jan-Jun;10(1):12-21. Review.(IF: 1.06)
|
2016 | |
| 391 |
None Association of XPD (Lys751Gln) and XRCC1 (Arg280His) gene polymorphisms in myelodysplastic syndrome.
Ann Hematol. 2016 Jan;95(1):79-85.(IF: 3.083)
|
2016 | |
| 392 |
None Antibody profile in Indian severe haemophilia A patients with and without FVIII inhibitors
Immunol Lett. 2016 Jan;169:93-7.(IF: 2.86)
|
2016 | |
| 393 |
None Second trimester prenatal diagnosis in Glanzmanns Thrombasthenia.
Haemophilia. 2015 Dec 28. [Epub ahead of print] (IF: 2.673)
|
2015 | |
| 394 |
None Challenges in Prenatal Diagnosis of Beta Thalassaemia: Couples with Normal HbA2 in One Partner.
Prenat Diagn. 2015 Dec;35(13):1353-7. (IF: 3.043)
|
2015 | |
| 395 |
None Differential expression of genes involved in Bengal macrothrombocytopenia (BMTCP).
Blood Cells Mol Dis. 2015 Dec;5(4):410-4. (IF: 2.731)
|
2015 | |
| 396 |
None Diverse phenotypes and transfusion requirements due to interaction of ?-thalassemias with triplicated ?-globin genes.
Ann Hematol. 2015 Dec;94(12):1953-8. (IF: 3.022)
|
2015 | |
| 397 |
None Molecular understanding of Indian untransfused thalassemia intermedia.
Int J Lab Hematol. 2015 Dec;37(6):791-6. (IF: 2.401)
|
2015 | |
| 398 |
None Effect of anticoagulant therapy on cell-derived microparticles and pregnancy outcome in women with pregnancy loss.
Br J Haematol. 2015 Dec;171(5):892-6. (IF: 5.812)
|
2015 | |
| 399 |
None Additional markers for genetic diagnosis of type 3 von Willebrand disease in Indian population.
Indian J Med Res. 2015 Dec;142(6):759-62. (IF: 1.446)
|
2015 | |
| 400 |
None Individualization of antiretroviral therapy Pharmacogenomic aspect.
Indian J Med Res. 2015 Dec;142(6):663-74. (IF: )
|
2015 | |
| 401 |
None Spectrum of mutations in Indian patients with fibrinogen disorders and its application in genetic diagnosis of the affected families.
Haemophilia. 2015 Nov;21(6):e519-23. (IF: 2.673)
|
2015 | |
| 402 |
None Association of clinical presentation with anti-nuclear antibody specificities among patients with systemic lupus erythematosus.
Indian J Nephrol. 2015 Nov-Dec;25(6):391-2 (IF: 0.55)
|
2015 | |
| 403 |
None Molecular analysis of Bombay phenotype cases seen in India.
ISBT Science Series 2015 Nov; 10(2):100-105. (IF: 0.39)
|
2015 | |
| 404 |
None Hepatitis B screening accuracy in blood bank.
Intl J Recent Scient Res 2015 Nov; 6(11): 7345-7357 (IF: 0.13)
|
2015 | |
| 405 |
None Experimental animal model to study iron overload and iron chelation and review of other such models.
Blood Cells Mol Dis. 2015 Oct;55(3):194-9. (IF: 2.731)
|
2015 | |
| 406 |
None Blood donation in Maharashtra: Prevalence of transfusion transmitted infections in blood donors.
Int J Pharm Bio Sci 2015 Oct; (4): (B) 981-987. (IF: 0.36)
|
2015 | |
| 407 |
None Inherited and acquired thrombophilia in Indian women experiencing unexplained recurrent pregnancy loss.
Blood Cells Mol Dis. 2015 Oct;55(3):200-5. (IF: 2.731)
|
2015 | |
| 408 |
None Genetic variations of hOCT1 gene and CYP3A4/A5 genes and their association with imatinib response in Chronic Myeloid Leukemia.
Eur J Pharmacol. 2015 Oct 15;765:124-30. (IF: 2.73)
|
2015 | |
| 409 |
None Association between the angiotensin-converting enzyme gene insertion/deletion polymorphism and susceptibility to systemic lupus erythematosus in an Indian population.
Scand J Rheumatol. 2015 Oct;44(5):425-7. (IF: 2.307)
|
2015 | |
| 410 |
None Trisomy 8 Mosaicism in a Boy with Dysmorphic Features.
Indian Pediatr. 2015 Sep;52(9):812-3. (IF: 0.972)
|
2015 | |
| 411 |
None A silent killer HCV (Hepatitis C virus) in India : A Review of prevalence from all available data
Intl J Curr Res, 2015 Sep; 7(9): 20193-20203. (IF: 0.08)
|
2015 | |
| 412 |
None Is peripheral blood corin level clinically relevant for prediction of pre-eclampsia?
Ultrasound Obstet Gynecol. 2015 Sep;46(3):380. (IF: 4.254)
|
2015 | |
| 413 |
None Tissue factor expressed by circulating cancer cell-derived microparticles drastically increases the incidence of deep vein thrombosis in mice: comment.
J Thromb Haemost. 2015 Sep;13(9):1737-8. (IF: 5.565)
|
2015 | |
| 414 |
None Low-Molecular-Weight Heparin for Women With Unexplained Recurrent Pregnancy Loss.
Ann Intern Med. 2015 Sep 15;163(6):483-4. (IF: 16.593)
|
2015 | |
| 415 |
None Sense, missense, and nonsense: a novel mechanism of premature termination codon (PTC) mutation in a severe von Willebrand disease (VWD) patient.
Ann Hematol. 2015 Aug;94(8):1409-10. (IF: 3.022)
|
2015 | |
| 416 |
None Genetic variations of hOCT1 gene and CYP3A4/A5 genes and their association with imatinib response in Chronic Myeloid Leukemia.
Eur J Pharmacol. 2015 Aug 21;765:124-130. (IF: 2.73 )
|
2015 | |
| 417 |
None Tyrosine kinase inhibitors: New class of antimalarials on the horizon?
Blood Cells Mol Dis. 2015 Aug;55(2):119-26. (IF: 2.18)
|
2015 | |
| 418 |
None Promising prognostic markers of preeclampsia: new avenues in waiting.
Thromb Res. 2015 Aug;136(2):189-95. Review. (IF: 2.32)
|
2015 | |
| 419 |
None Emerging Proteomic and Glycoproteomic biomarkers for Hepatocellular carcinoma.
Intl J Res Engg Applied Sci 2015Aug; 5(8): 76-89. (IF:)
|
2015 | |
| 420 |
None Erratum to: A novel ELISA for diagnosis of Glanzmanns thrombasthenia and the heterozygote carriers.
Ann Hematol. 2015 Jul;94(7):1259. (IF: 3.022)
|
2015 | |
| 421 |
None High heterozygosity frequency of three exonic SNPs of factor V gene (F5): implications for genetic diagnosis.
Indian J Med Res. 2015 Jul;142(1):85-7. (IF: 1.446)
|
2015 | |
| 422 |
None A successful twin pregnancy in a patient with HbE-?-thalassemia in western India.
J Postgrad Med. 2015 Jul-Sep;61(3):203-5. (IF: 0.87)
|
2015 | |
| 423 |
None Morphological Spectrum of Paroxysmal Nocturnal Hemoglobinuria (PNH).
Indian J Hematol Blood Transfus. 2015 Jun;31(2):314-6. (IF: 0.232)
|
2015 | |
| 424 |
None Factors Modulating Blood HbA1C Level and Diabetic Retinopathy.
J Assoc Physicians India. 2015 May;63(5):95-6. (IF: 0.37)
|
2015 | |
| 425 |
None Tetrasomy X in a Child with Upper Limb Deformity.
Indian Pediatr. 2015 May;52(5):439. (IF: 0.972 )
|
2015 | |
| 426 |
None Prenatal diagnosis in a haemophilia carrier with triplet pregnancy.
Haemophilia. 2015 May;21(3):e228-30. (IF: 2.673 )
|
2015 | |
| 427 |
None Glucose-6-phosphate dehydrogenase (G6PD) deficiency among tribal populations of India - Country scenario.
Indian J Med Res. 2015 May;141(5):516-20. (IF: 1.446)
|
2015 | |
| 428 |
None Paradoxical bleeding and thrombosis in a patient with afibrinogenemia and fibrinogen Mumbai mutation.
Am J Clin Pathol. 2015 May;143(5):755-. (IF: 2.278)
|
2015 | |
| 429 |
None Leukocyte adhesion deficiency-I with a novel intronic mutation presenting with pyoderma gangrenosum- like lesions.
J Clin Immunol. 2015 May;3(4):431-4. (IF: 3.094 )
|
2015 | |
| 430 |
None Haemoglobinopathies in tribal populations of India.
Indian J Med Res. 2015 May;141(5):505-8. (IF: 1.446)
|
2015 | |
| 431 |
None Sickle cell disease in tribal populations in India.
Indian J Med Res. 2015 May;141(5):509-15. (IF: 1.446 )
|
2015 | |
| 432 |
None Sickle cell anaemia: The need for new approaches in management.
Natl Med J India. 2015 Mar-Apr;28(2):90-3. (IF: 0.907)
|
2015 | |
| 433 |
None Prenatal diagnosis in a family with purfura fulminans.
Blood Coagul Fibrinolysis. 2015 Apr;26(3):350. (IF: 1.242 )
|
2015 | |
| 434 |
None Hb M Hyde Park and Hb M Boston in two Indian families - a rare cause of methaemoglobinemia.
Int J Lab Hematol. 2015 Apr;37(2):e40-3. (IF: 2.401)
|
2015 | |
| 435 |
None Hepatitis B Diagnosis in Blood Bank: Evaluation and Challenges
MGM J Med Sci 2015 Apr-Jun; 2 (2) : 83-89 (IF: )
|
2015 | |
| 436 |
None Nanoimaging in cardiovascular diseases: Current state of the art.
Indian J Med Res. 2015 Mar;141(3):285-98. (IF: 1.446 )
|
2015 | |
| 437 |
None Syndrome due to CD40 Deficiency: Possibly the first case from India.
Journal of Postgraduate Medicine. 2015 Jan-Mar; 61:41-48. (IF: 0.87 )
|
2015 | |
| 438 |
None Feasibility of a Newborn screening and follow-up programme for sickle cell disease among South Gujarat (India) tribal populations.
J Med Screen 2015 Mar;22(1):1-7 (IF: 1.75)
|
2015 | |
| 439 |
None The Prevalence of Factor V Leiden (G1691A) and Methylenetetrahydrofolate Reductase C677T Sickle Cell Disease in Western India. Mutations in
Clin Appl Thromb Hemost. 2015 Mar;21(2):186-9.(IF: 1.973)
|
2015 | |
| 440 |
None Spectrum of red cell abnormalities in undiagnosed hemolytic anemias and methemoglobinemias: a single center experience.
Clin Chem Lab Med 2015 Mar1;53(4):e105-8. (IF: 3.017 )
|
2015 | |
| 441 |
None Challenges and open issues in the management of acquired hemophilia A (AHA).
Blood Cells Mol Dis. 2015 Mar;54(3):275-80.Review.(IF: 2.731)
|
2015 | |
| 442 |
None Spectrum of perforin gene mutations in familial hemophagocytic lymphohistiocytosis (FHL) patients in India
Blood Cells Mol Dis. 2015 Mar;54(3):250-7. (IF: 2.731 )
|
2015 | |
| 443 |
None Spectrum of Hemoglobinopathies Among the Primitive Tribes: A Multicentric Study in India.
Asia Pac J Public Health. 2015 Mar;27(2):NP562-71 (IF: 1.05)
|
2015 | |
| 444 |
None Neuropsychiatric manifestations and associated autoantibodies in systemic lupus erythematosus patients from Western India.
Rheumatol Int. 2015 Mar;35(3):541-5. (IF: 1.702)
|
2015 | |
| 445 |
None Erythrocytosis, methemoglobinemia, and the saturation gap.
Ann Hematol. 2015 Mar;94(3):509-10.(IF: 3.022)
|
2015 | |
| 446 |
None Molecular characterization of leukocyte adhesion deficiency-I in Indian patients: identification of 9 novel mutations.
Blood Cells Mol Dis. 2015 Mar;54(3):217-23. (IF: 2.731)
|
2015 | |
| 447 |
None Novel therapeutic approaches for haemophilia.
Haemophilia 2015 Mar;21(2):152-61. (IF: 2.673 )
|
2015 | |
| 448 |
None Do UGT1A1 and HMOX1 gene promoter polymorphisms increase the risk of hyperbilirubinemia and gallstones in patients with hereditary spherocytosis?
Ann Hematol. 2015 Jan;94(1):169-71. (IF: 3.022)
|
2015 | |
| 449 |
None Mannose binding lectin (MBL) 2 gene polymorphism & its association with clinical manifestations in systemic lupus erythematosus (SLE) patients from western India.
Indian J Med Res. 2015 Feb;141(2):199-204. (IF: 1.446)
|
2015 | |
| 450 |
None Evolution of BCR/ABL gene mutation in CML is time dependent and dependent on the pressure exerted by tyrosine kinase inhibitor
PLoS One. 2015 Jan 28;10(1):e0114828. eCollection 2015. (IF: 3.057)
|
2015 | |
| 451 |
None Variable phenotypes of sickle cell disease in India with the Arab-Indian haplotype.
Br J Haematol. 2015 Jan;168(1):156-9. (IF: 5.812)
|
2015 | |
| 452 |
None Clinical spectrum and molecular basis of recessive congenital methemoglobinemia in India.
Clin Genet. 2015 Jan;87(1):62-7. (IF: 3.892)
|
2015 | |
| 453 |
None Effect of proinflammatory cytokines (IL-6, TNF-?, and IL-1?) on clinical manifestations in Indian SLE patients.
Mediators Inflamm. 2014;2014:385297.Epub 2014 Dec 7.
|
2014 | |
| 454 |
None Primaquine-induced severe methemoglobinemia developed during treatment of Plasmodium vivax malarial infection in an Indian family associated with a novel mutation (p.Agr57Trp) in the CYB5R3 gene.
Clin Chim Acta 2014 Nov1; 437:103-5.(IF:2.764)
|
2014 | |
| 455 |
None Unusual clinical presentations of familial hemophagocytic lymphohistiocytosis Type-2.
J Pediat Hematol Oncol 2014 Nov; 36(8):e524-7.(iF:0.973)
|
2014 | |
| 456 |
None Hemoglobinopathy Screening by Osmotic Fragility Test Based on Flow Cytometer or Naked Eye
Cytometry B Clin Cytom. 2014 Nov 24. [Epub ahead of print](IF:2.824)
|
2014 | |
| 457 |
None HbD Punjab/HbQ India Compound Heterozygosity: An Unusual Association.
Mediterr J Hematol Infect Dis. 2014 Nov 1;6(1):e2014072. eCollection 2014.(IF:-)
|
2014 | |
| 458 |
None Rapid flow cytometry based cytotoxicity assay for evaluation of NK cell function
Indian J Exp Biol 2014 Oct; 52(10):983-8.(IF:0.835)
|
2014 | |
| 459 |
None Molecular pathology of rare bleeding disorders (RBDs) in India: A systematic review.
PLos One 2014 Oct 2; 9(9):e108683.(IF:3.534)Review
|
2014 | |
| 460 |
None Paternal factor V Leiden and recurrent pregnancy loss: a new concept behind fetal genetics?: comment
J Thromb Haemost. 2014 Oct; 12(10):1758-9.(IF:5.72)
|
2014 | |
| 461 |
None Role of co-inherited Gilbert syndrome on hyperbilirubinemia in Indian beta thalassemia patients
Hematology 2014 Oct; 19(7):388-92.(IF:1.393)
|
2014 | |
| 462 |
None Clinical and autoimmune profile of scleroderma patients from Western India
Int J Rheumatol. 2014;2014:983781. Epub 2014 Oct 19.(IF:1.469)
|
2014 | |
| 463 |
None Analysis of F8 inversions as risk factors for FVIII inhibitor development in Indian severe haemophilia A patients
Blood Cells Mol Dis 2014 Sep; 53(3):161-3.(IF:2.331)
|
2014 | |
| 464 |
None VKORC1 and CYP2C9 genotype distribution in Asian countries.
Thromb Res. 2014 Sep; 134(3):537-44.(IF:3.133)
|
2014 | |
| 465 |
None Acquired and Heritable Thrombophilia in Indian Patients With Pediatric Deep Venous Thrombosis (DVT).
Clin Appl Thromb Hemost. 2014 Sep;20(6):573-6 (IF: 1.332)
|
2014 | |
| 466 |
None X-linked hyper IgM syndrome: Clinical, immunological and molecular features in patients from India
Blood Cells Mol Dis. 2014 Sep; 53(3):99-104.(IF:2.331)
|
2014 | |
| 467 |
None The association of HLA-DRB1 and HLA-DQB1 alleles with the development of factor VIII inhibitors in severe haemophilia A patients in India.
Tissue Antigens 2014 Aug; 84(2):235-7.(IF:2.35)
|
2014 | |
| 468 |
None Is thrombophilia associated with placenta-mediated pregnancy complications? A prospective cohort study: comment
J Thromb Haemost. 2014 Aug; 12(8):1377-8.(IF:5.72)
|
2014 | |
| 469 |
None Combined protein and nucleic acid-level effects of rs1143679(R77H), a lupus-predisposing variant within ITGAM.
Hum Mol Genet 2014 Aug 1; 23(15):4161-76.(IF:6.393)
|
2014 | |
| 470 |
None Combined effects of the UGT1A1 and OATP2 gene polymorphisms as major risk factor for unconjugated hyperbilirubinemia in Indian neonates
Gene. 2014 Aug 15;547(1):18-22.(IF:2.443)
|
2014 | |
| 471 |
None Rare coagulation factor deficiencies: a countrywide screening data from India.
Haemophilia. 2014 Jul; 20(4):575-81.(IF:3.170)
|
2014 | |
| 472 |
None Isodicentric Philadelphia [idic(Ph)] chromosome in a case of CML at chronic phase
Indian J Cancer. 2014 July-September;51(3):383-384.(IF:0.802)
|
2014 | |
| 473 |
None Prenatal detection of Fanconi anemia.
Indian Pediatr. 2014 Jun;51(6):501
|
2014 | |
| 474 |
None Down-regulation of miR-199b associated with imatinib drug resistance in 9q34.1 deleted BCR/ABL positive CML patients.
Gene. 2014 Jun 1;542(2):109-12.(IF:2.082)
|
2014 | |
| 475 |
None Hb Koln [?98(FG5) [GTG ? ATG, Val ? Met]]: the first report from India.
Hematology. 2014 Jun;19(4):199-201.(IF:1.393)
|
2014 | |
| 476 |
None Factor VIII Antigen, Activity, and Mutations in Hemophilia A.
Clin Appl Thromb Hemost. 2014 May;22(4):381-5.
|
2014 | |
| 477 |
None Factor V Leiden mutation modulates the bleeding phenotype in warfarin sensitive patients.
Thromb Res. 2014 May;133(5):955-6(IF:2.427)
|
2014 | |
| 478 |
None Mutations in intron 1 and intron 22 inversion negative haemophilia a patients from Western India
PLoS One. 2014 May 20;9(5):e97337. eCollection 2014.(IF:3.534)
|
2014 | |
| 479 |
None Sickle cell disease in India.
Curr Opin Hematol. 2014 May;21(3):215-23.(IF:4.053)
|
2014 | |
| 480 |
None Distribution of HLA-DR?1 alleles among well-characterized rheumatoid arthritis patients from Western India.
Rheumatol Int. 2014 May;34(5):705-8.(IF:1.516)
|
2014 | |
| 481 |
None Fetal hemoglobin in sickle cell anemia
Blood Cells Mol Dis. 2014 Apr;52(4):175.(IF:2.331)
|
2014 | |
| 482 |
None Guidelines for screening, diagnosis and management of hemoglobinopathies
Indian J Hum Genet. 2014 Apr;20(2):101-19. Review.
|
2014 | |
| 483 |
None Methylenetetrahydrofolatereductase C677T polymorphism and folate metabolism in
Indian J Hum Genet. 2014 Apr;20(2):99-100
|
2014 | |
| 484 |
None Prenatal diagnosis in severe von Willebrand disease families from India using combination of phenotypic and genotypic assays
Prenat Diagn 2014 Apr; 34(4):377-81.(IF:3.296)
|
2014 | |
| 485 |
None FLT3 and NPM-1 mutations in a cohort of acute promyelocytic leukemia patients from
Indian J Hum Genet. 2014 Apr;20(2):160-5.
|
2014 | |
| 486 |
None Clinical and hematological presentation among Indian patients with common hemoglobin variants.
Clin Chim Acta 2014 Apr 20; 431:46-51.(IF:2.824)
|
2014 | |
| 487 |
None Rapid Flow Cytometric Prenatal Diagnosis of Primary Immunodeficiency (PID)
J Clin Immunol 2014 Apr; 34(3):316-22.(IF:3.184)
|
2014 | |
| 488 |
None Delayed Vitamin K deficiency related bleeding: is it genetically linked?
Indian J Pediatr. 2014 Mar;81(3):310-1. (IF:0.919)
|
2014 | |
| 489 |
None A specific and sensitive activated partial thromboplastin time (APTT)-based factor VIII inhibitor screening assay
Clin Chem.Lab Med. 2014 Mar;52(3):e39-41.(IF:2.955)
|
2014 | |
| 490 |
None Genetic heterogeneity in a large cohort of Indian type 3 von Willebrand disease patients
PLoS One. 2014 Mar 27;9(3):e92575. (IF:3.534)
|
2014 | |
| 491 |
None Novel genetic abnormalities in Bernard-Soulier syndrome in India
Ann Hematol. 2014 Mar;93(3):381-4. (IF:2.396)
|
2014 | |
| 492 |
None Genetic thrombophilia and natural anticoagulants: importance of polymorphisms within
Haematologica. 2014 Mar;99(3):e30. (IF:5.868)
|
2014 | |
| 493 |
None Masking of a ?-thalassemia determinant by a novel ??globin gene defect [Hb A2-Saurashtra or ?????G2)Pro®Ser; HBD: C.301C>T] in Cis
Hemoglobin 2014 Jan-Feb; 38(1):24-7. .(IF:0.955)
|
2014 | |
| 494 |
None Hemoglobin variants in Muslim community in South Gujarat, Western India.
Int J Lab Hematol. 2014 Feb;36(1):e15-7 (IF: 1.176)
|
2014 | |
| 495 |
None Molecular characterization of weaker variants of A and B in Indian population- the first report.
Tranf Apheresis Sci 2014 Feb; 50(1): 118-22.(IF:1.072)
|
2014 | |
| 496 |
None Chimeric Fusion Karyotypes in Childhood B-cell Acute Lymphoblastic Leukemia
Indian Pediatr. 2014 Feb 8;51(2):152-3.(IF:1.036)
|
2014 | |
| 497 |
None Molecular genotyping of ABO blood groups in some population groups from India.
Indian J Med Res 2014 Jan; 139(1): 105-111. (IF: 1.661)
|
2014 | |
| 498 |
None An atypical manifestation of acquired von Willebrand syndrome (AVWS) associated with systemic lupus erythematosus (SLE).
Ann Hematol. 2014 Jan; 93(1): 173-5. (IF:2.396)
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2014 | |
| 499 |
None Role of hla-B alleles and clinical presentation of b27 negative spondyarthritis patients from Mumbai, Western India
Autoimmune Dis. 2014;2014:327315. Epub 2014 Mar 6. (IF:--)
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2014 | |
| 500 |
None Neurometabolic Disorder with Microcephaly, Dystonia and Central Cyanosis Masquerading as Cerebral Palsy
J Child Neurol 2014 Jan 1-4.(IF:1.717)
|
2014 | |
| 501 |
None Pattern of chromosome involvement in childhood hyperdiploid pre-B-cell acute lymphoblastic leukemia cases from India
Indian J Hum Genet. 2014 Jan;20(1):32-6. .(IF:--)
|
2014 | |
| 502 |
None Thalassemias: can we reduce the national burden ?
Mol Cytogenet 2014 Jan 21; 7 (Suppl 1 proceedings of the international conference on Human): I43. (IF:2.66)
|
2014 | |
| 503 |
None Haemophilia- diagnosis and management challenges
Mol Cytogenet 2014 Jan 21; 7 (Suppl 1 proceedings of the international conference on Human): I44. .(IF:2.66)
|
2014 | |
| 504 |
None Familial Mediterranean fever: An unusal disease enlightening the inflammation biology
Indian J Hum Genet. 2014 Jan; 20(1):1-3. (IF:--)
|
2014 | |
| 505 |
None X linked agammaglobulinemia: a single centre experience from India
Indian J Pediatr 2014 Jan; 81(1):92-4. (IF:0.919)
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2014 | |
| 506 |
None Dr. Bhatias legacy in the development of immunohematology research in the country
Asian J Transfus Sci. 2014;8(Suppl 1):S1-2.
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2014 | |
| 507 |
None Chromosomal instability and molecular mutations in multi spectrum disease of Fanconi anemia
Mol Cytogenet 2014 Jan 21; 7 (Suppl 1 proceedings of the international conference on Human): I47. .(IF:2.66)
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2014 | |
| 508 |
None Application of a Simple In-House PCR-SSP Technique for HLA-B* 27 Typing in Spondyloarthritis Patients.
Arthritis. 2013;2013:504109. doi: 10.1155/2013/504109. Epub 2013 Dec 19.
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2013 | |
| 509 |
None Pulmonary hydatidosis, strongyloidiasis and paragonimiasis in India.
J Assoc Physicians India. 2013 Dec;61(12):954-5
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2013 | |
| 510 |
None Evaluation of danazol, cyclosporine, and prednisolone as single agent or in combination
Turk J Haematol. 2013 Dec;30(4):366-70.(IF:0.34)
|
2013 | |
| 511 |
None Molecular characterization of ?-thalassemia in four communities in South Gujarat-codon
Ann Hematol. 2013 Nov;92(11):1473-6. (IF:2.615)
|
2013 | |
| 512 |
None Anti-C reactive protein antibodies in Indian patients with systemic lupus erythematosus
Indian J Nephrol 2013 Nov; 23(6): 434-7.
|
2013 | |
| 513 |
None DNA interstrand cross-link repair: understanding role of Fanconi anemia pathway and
Eur J Haematol. 2013 Nov;91(5):381-93 (IF:2.066)
|
2013 | |
| 514 |
None Molecular pathology of Bernard-Soulier syndrome in Indian patients
Platelets. 2013 Nov; 24(7):571-3.(IF: 2.391)
|
2013 | |
| 515 |
None Investigating cell surface markers on normal hematopoietic stem cells in three different
Int J Stem Cells. 2013 Nov;6(2):129-33.(IF:0.625)
|
2013 | |
| 516 |
None Single low-dose un-adjuvanted HBsAg nanoparticle vaccine elicits robust , durable immunity.
Nanomedicine 2013 Oct; 9(7):923-34. (IF: 5.26)
|
2013 | |
| 517 |
None Efficacy of Fixed Low Dose Hydroxyurea in Indian Children with Sickle Cell Anemia: A
Indian Pediatr. 2013 Oct;50(10):929-33 (IF :)
|
2013 | |
| 518 |
None Molecular and clinical heterogeneity in pyruvate kinase deficiency in India.
Blood Cells Mol Dis. 2013 Oct;51(3): 133-7.(IF: 2.361)
|
2013 | |
| 519 |
None Polymorphisms of warfarin metabolizing enzymes in an Indian population
Blood Cells Mol Dis. 2013 Oct; 51(3):203.(IF: 2.361)
|
2013 | |
| 520 |
None A novel 5-way translocation t(9;11;13;19;22) in a case of chronic-phase chronic myeloid
Hum Pathol. 2013 Oct; 44(10):2365-9.(IF: 3.077)
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2013 | |
| 521 |
None A specific and sensitive activated partial thromboplastin time (APTT)-based factor VIII
Clin Chem Lab Med. 2013 Oct 2:1-3.(2.955)
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2013 | |
| 522 |
None Transfusion transmitted infections in Indian thalassemics: a perspective
Indian J Hematol Blood Transfus. 2013 Sep;29(3):189-90.
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2013 | |
| 523 |
None The genetics of Canadian type 3 von Willebrand disease: further evidence for co-dominant inheritance of mutant alleles: a rebuttal.
J Thromb Haemost. 2013 Sep; 11(9): 1784-5.(IF: 5.731)
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2013 | |
| 524 |
None Matrix metalloproteinase and its drug targets therapy in solid and hematological malignancies: An overview.
Mutat Res. 2013 Jul-Sep; 753(1):7-23.(IF: 3.680)
|
2013 | |
| 525 |
None Multifactorial aetiology for bone disease in patients with haemophilia.
Eur J Haematol. 2013 May;90(5):435(IF:2.066)
|
2013 | |
| 526 |
None A common founder mutation p.P2063S in exon 36 of VWF in 11 unrelated Indian von Willebrand disease (VWD) families
Ann Hematol. 2013 Aug; 92(8):1147-9. (IF: 2.615)
|
2013 | |
| 527 |
None Prevalence of clinically relevant (TA)n UGT1A1 promoter alleles in Indian neonates
Curr Sci 2013 Aug; 105(4): 446-7. (IF: 0.933 )
|
2013 | |
| 528 |
None Mitochondrial DNA variations in myelodysplastic syndrome
Ann Hematol. 2013 Jul;92(7): 871-6. (IF: 2.615)
|
2013 | |
| 529 |
None Hereditary thrombophilia in cerebral venous thrombosis: a study from India.
Blood Coagul Fibrinolysis. 2013 Jul; 24(5):540-3.(IF:1.238)
|
2013 | |
| 530 |
None Role of microparticles in recurrent miscarriages and other adverse pregnancies: a review.
Eur J Obstet Gynecol Reprod Biol. 2013 Jul; 169(2):123-9.(IF:1.974)
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2013 | |
| 531 |
None Molecular organization of Rh gene is likely to be heterogeneous across the world.
Asian J Transfus Sci. 2013 Jul;7(2):103-4.
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2013 | |
| 532 |
None Factor VIII haplotypes in severe hemophilia A patients in India
Ann Hematol. 2013 Jul; 92(7): 999-1000.(IF: 2.615)
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2013 | |
| 533 |
None Profibrinolytic microparticles are not adequately produced to compensate their
Haematologica. 2013 Jul;98(7):e69.(IF:5.868)
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2013 | |
| 534 |
None Acquired von Willebrand syndrome: A rare disorder of heterogeneous etiology.
J Postgrad Med. 2013 Apr-Jun;59(2):98-101.(IF: 1.389)
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2013 | |
| 535 |
None A study on anti-mannose binding lectin (anti-MBL) antibodies and serum MBL levels in
Rheumatol Int 2013 Jun; 33(6): 1533-9.(IF: 1.885)
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2013 | |
| 536 |
None The angiotensin-converting enzyme gene insertion/deletion polymorphism in Indian vitiligo patients: a case-control study and meta-analysis
Br J Dermatol. 2013 Jun; 168(6): 1195-1204.(IF: 3.666)
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2013 | |
| 537 |
None Variable Presentation of HB H Disease Due to Homozygosity for the Rare Polyadenylation Signal a TIndian (AATAAA>AATA- -) Mutation in Four Indian Families.
Hemoglobin. 2013 May-Jun; 37(3): 277-84.(IF: 1.304)
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2013 | |
| 538 |
None Influence of CYP2C9 and VKORC1 gene polymorphisms on warfarin dosage, over
Eur J Pharmacol. 2013 Jun 15;710(1-3):80-4.(IF:2.684)
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2013 | |
| 539 |
None Diagnostic approach to primary immunodeficiency disorders.
Indian Pediatr. 2013 Jun 8;50(6):579-86.(IF:1.044)
|
2013 | |
| 540 |
None New missense homozygous mutation (Q270Ter) in the pyrimidine 5 nucleotidase type I-related gene in two Indian families with hereditary non-spherocytic hemolytic anemia
Ann Hematol. 2013 May;92(5):715-7. (IF: 2.615)
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2013 | |
| 541 |
None Methylation status of imprinted genes DLK1-GTL2, MEST (PEG1), ZAC (PLAGL1),
Fertil Steril. 2013 May;99(6):1668-73.
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2013 | |
| 542 |
None Maternal and neonatal outcomes in gestational diabetes mellitus
J Indian Med Assoc. 2013 May;111(5):330-1, 336.
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2013 | |
| 543 |
None Comprehensive Report of Primary Immunodeficiency Disorders from a Tertiary Care Center in India
J Clin Immunol. 2013 Apr; 33(3):507-12.(IF:3.077)
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2013 | |
| 544 |
None Immunological disturbances associated with malarial infection
J Parasitic Dis 2013 Apr;37(1):11-15. Review.
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2013 | |
| 545 |
None Comparison of in-vitro and in-vivo response to fetal hemoglobin production and ?-mRNA expression by hydroxyurea in Hemoglobinopathies
Indian J Hum Genet. 2013 Apr;19(2):251-8.
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2013 | |
| 546 |
None Clinical and Immunological profile of systemic lupus erythematosus
Indian Pediatr 2013 Apr 8; 50(4): 405-7.(IF: 1.048)
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2013 | |
| 547 |
None Antenatal screening for identification of couples for prenatal diagnosis of severe
J Obstet Gynaecol India. 2013 Apr;63(2):123-7.
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2013 | |
| 548 |
None HLA-DR?1*04 typing by simple in-house PCR-SSP technique for rheumatoid arthritis patients.
Rheumatol Int. 2013 Apr; 33(4): 867-70.(IF: 2.200)
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2013 | |
| 549 |
None Identification of a novel large intragenic deletion in a family with Fanconi Anemia: First
Gene. 2013 Apr 15; 518(2): 470-5. (IF:2.443)
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2013 | |
| 550 |
None Vitiligo patients from India (Mumbai) show differences in clinical, demographic and autoantibody profiles compared to patients in western countries
J Eur Acad Dermatol Venereol. 2013 Mar;27(3):279-86.
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2013 | |
| 551 |
None Cytogenetics in paediatric aplastic anaemia: does it give an insight on the evolution of the disease?
Indian J Med Res. 2013 Mar;137(3):445-6.(IF: 1.837).
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2013 | |
| 552 |
None Effect of a group of genetic markers around the 5 regulatory regions of the ? globin gene cluster linked to high HbF on the clinical severity of ? thalassemia.
Blood Cells Mol Dis. 2013 Mar;50(3):156-60.(IF:2.361)
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2013 | |
| 553 |
None Detection of fetal mutations causing hemoglobinopathies by non-invasive prenatal
J Postgrad Med. 2013 Jan-Mar;59(1):15-20. (IF: 1.389)
|
2013 | |
| 554 |
None The myriad effects of cigarette smoke.
J Thromb Haemost. 2013 Feb;11(2):387-8.(IF: 5.731)
|
2013 | |
| 555 |
None Autoimmune lymphoproliferative syndrome caused by a homozygous null FAS ligand (FASLG) mutation
J Allergy Clin Immunol. 2013 Feb;131(2):486-90.(IF: 11.003)
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2013 | |
| 556 |
None Delayed warfarin induced skin necrosis in a patient with poor warfarin metabolizing activity due to interrupted warfarin therapy
Eur J Clin Pharmacol. 2013 Feb;69(2):293-4.(IF: 2.845)
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2013 | |
| 557 |
None Prevalence of factor V G1691A, factor II G20210A, methylenetetrahydrofolate reductase C677T and endothelial protein C receptor 23 bp insertion polymorphisms in indigenous population of Nepal.
Ann Hematol. 2013 Jan;92(2):261-2. (IF: 2.615)
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2013 | |
| 558 |
None A simple diagnostic strategy for RhD typing in discrepant cases in the Indian population
Blood Transfus. 2013 Jan;11(1):37-42. (IF: 2.099).
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2013 | |
| 559 |
None UDP-glucuronosyltransferase 1A1 (UGT1A1) gene haplotypes and their effect on serum bilirubin concentration in healthy Indian adults.
Gene. 2013 Jan 15;513(1):36-9.(IF:2.443)
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2013 | |
| 560 |
None Prevalence of ?-thalassemia and other haemoglobinopathies in six cities in India: a
J Community Genet. 2013 Jan;4(1):33-42.
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2013 | |
| 561 |
None Effect of Cis Acting Potential Regulators in the ? Globin Gene Cluster on the Production of HbF in Thalassemia Patients.
Mediterr J Hematol Infect Dis. 2013; 5(1): e2013012. Published online 2013 February 16.(IF: )
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2013 | |
| 562 |
None Hemoglobin variants and high-performance liquid chromatography.
Int J Lab Hematol. 2013 Jan 11. [Epub ahead of print] .(IF: 1.176)
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2013 | |
| 563 |
None Recessive congenital methemoglobinemia due to NADH-cytochrome b5 reductase deficiency associated with recurrent early pregnancy loss (REPL) in an Indian family
Ann Hematol. 2012 Dec;91(12):1985-6. (IF: 2.615)
|
2012 | |
| 564 |
None Prenatal Diagnosis of LAD-I on Cord Blood by Flowcytometry.
Indian J Pediatr. 2012 Dec;79(12):1605-9.(IF: 0.521)
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2012 | |
| 565 |
None Clinical and serological features of male Systemic Lupus Erythematosus patients from Western India
Indian J Rhematol 2012 Dec; 7(4):204-8.
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2012 | |
| 566 |
None FLT3 and NPM1 mutations in a cohort of AML patients and detection of a novel mutation in tyrosine kinase domain of FLT3 gene from Western India.
Ann Hematol. 2012 Nov;91(11):1703-12. (IF: 2.615)
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2012 | |
| 567 |
None Research update for articles published in EJCI in 2010
Eur J Clin Invest 2012 Nov; 42(11):1149-64.(If: 3.365)
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2012 | |
| 568 |
None APTT reagents for different coagulation tests: one size does not fit all
Am J Clin Pathol. 2012 Nov;138(5):757; author reply 757-8.
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2012 | |
| 569 |
None Non conventional mutations associated with myeloproliferative disorders are absent in splanchnic venous thrombosis cases
Liver Int. 2012 Nov;32(10):1596-7.(IF: 3.824)
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2012 | |
| 570 |
None Sickle Cell Disease from Central India: A Retrospective Analysis.
Indian Pediatr. 2012 Nov;49(11):911-3. (IF:1.048)
|
2012 | |
| 571 |
None Standard karyotyping concentrates microfilaria and can be a valid concentrating technique for their detection
Trop Med Int Health. 2012 Oct;17(10):1222-6.(IF: 2.795)
|
2012 | |
| 572 |
None Prothrombin Mumbai causes severe prothrombin deficiency due to a novel Cys90Ser mutation.
Ann Hematol. 2012 Oct;91(10):1667-8.(IF: 2.615)
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2012 | |
| 573 |
None Compromising for carrier detection of beta thalassemia based on measurement of HbA2 levels in unusual cases
Clin Chim Acta. 2012 Oct 9;413(19-20):1705-7.(IF:2.661)
|
2012 | |
| 574 |
None Immune regulatory gene polymorphisms as predisposing risk factors for the development of factor VIII inhibitors in Indian severe haemophilia A patients
Haemophilia. 2012 Sep;18(5):794-7.(IF: 2.597)
|
2012 | |
| 575 |
None G71R mutation of the UGT1A1 gene is not associated with neonatal hyperbilirubinemia in India.
J Matern Fetal Neonatal Med. 2012 Sep; 25(9):1833-4.(IF: 1.592)
|
2012 | |
| 576 |
None Study of PTPN22 1858C/T polymorphism in rheumatoid arthritis patients from Western India.
Indian J Rheumatol 2012 Sep; 7(3):130-134.(IF: )
|
2012 | |
| 577 |
None Hereditary protein C deficiency in Indian patients with venous thrombosis.
Ann Hematol. 2012 Sep;91(9):1471-6.(IF: 2.615)
|
2012 | |
| 578 |
None Anti-C1q antibodies and their association with complement components in Indian systemic lupus erythematosus patients
Indian J Nephrol. 2012 Sep;22(5):353-7.
|
2012 | |
| 579 |
None APO1/F as promoter polymorphism in systemic lupus erythematosus (SLE): significance in clinical expression of the disease
J Assoc Physicians India. 2012 Sep; 60:34-7.(IF:)
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2012 | |
| 580 |
None Bone health in persons with haemophilia (PWH): A review.
Eur J Haematol.2012 Aug;89(2):95-102.(IF: 2.614)
|
2012 | |
| 581 |
None Subclinical iron deficiency is a silent epidemic amongst voluntary blood donors.
Transfus Med. 2012 Aug;22(4):300-1. (IF:1.14)
|
2012 | |
| 582 |
None Newborn screening shows a high incidence of sickle cell anemia in Central India.
Hemoglobin. 2012 Jul-Aug; 36(4):316-22.(IF: 1.304)
|
2012 | |
| 583 |
None Malignancies in persons with haemophilia: 25-year data from India.
Natl Med J India. 2012 Jul-Aug;25(4):251.(IF: 0.595)
|
2012 | |
| 584 |
None Toll-like receptors in autoimmunity with special reference to systemic lupus erythematosus
Indian J Hum Genet 2012 May-Aug; 18(2): 155-60.
|
2012 | |
| 585 |
None Hereditary non-spherocytic hemolytic anemia and severe glucose phosphate isomerase deficiency in an Indian patient homozygous for the L487F mutation in the human GPI gene.
Int J Hematol. 2012 Aug;96(2):263-7. (IF: 1.268)
|
2012 | |
| 586 |
None Variable haematological and clinical presentation of ?-thalassaemia carriers and homozygotes with the Poly A (T?C) mutation in the Indian population.
Eur J Haematol. 2012 Aug;89(2):160-4. (IF: 2.614)
|
2012 | |
| 587 |
None Prenatal diagnosis of HbE-Lepore and Hb Lepore-?-thalassemia: the importance of accurate genotyping of the couple at risk.
Prenat Diagn. 2012 Jul;32(7):703-7.(IF: 2.106)
|
2012 | |
| 588 |
None First case of Hb Fontainebleau with sickle haemoglobin and other non-deletional ? gene variants identified in neonates during newborn screening for sickle cell disorders.
J Clin Pathol. 2012 Jul;65(7):654-9.(IF: 2.306)
|
2012 | |
| 589 |
None A simple diagnostic strategy for RhD typing in discrepant cases in the Indian population.
Blood Transfus 2012 Jul; 12: 1-6. (IF: 2.099)
|
2012 | |
| 590 |
None A profile of rare bloods in India and its impact in blood transfusion service.
Asian J Transf Sci 2012 Jan-Jun; 6(1): 42-43.
|
2012 | |
| 591 |
None Cancers in patients with hemophilia: a retrospective study from the Italian Association of Hemophilia Centers: a rebuttal.
J Thromb Haemost. 2012 Jun;10(6):1200-1; author reply 1201-2. (IF: 5.731)
|
2012 | |
| 592 |
None A novel ELISA for diagnosis of Glanzmanns thrombasthenia and the heterozygote carriers.
Ann Hematol. 2012 Jun; 91(6):917-21.(IF: 2.615)
|
2012 | |
| 593 |
None Cause of deep venous thrombosis and pulmonary embolism in young patients from India as compared with other ethnic groups.
Blood Coagul Fibrinolysis. 2012 Jun;23(4):257-61.(IF: 1.25)
|
2012 | |
| 594 |
None A new simple approach for the determination of pyrimidine 5-nucleotidase activity in human erythrocytes using an ELISA reader.
Int J Lab Hematol. 2012 Jun; 34(2): 232-4.(IF: 1.176)
|
2012 | |
| 595 |
None Haematology research in India: past, present and future.
Indian J Hematol Blood Transfus. 2012 Jun;27(2):55-64. (IF: 0.056)
|
2012 | |
| 596 |
None Imatinib resistance due to a novel tri-nucleotide insertion in the SH2/C lobe interface of BCR/ABL kinase domain between position K357 and N358.
Leuk Res. 2012 May;36(5):e110-2.(2.472)
|
2012 | |
| 597 |
None A homozygous female hemophilia A.
Indian J Hum Genet 2012 Jan-Apr; 18(1): 134-6.
|
2012 | |
| 598 |
None Hemostasis Research in India: Past, Present, and Future.
Clin Appl Thromb Hemost. 2012 Mar-Apr;18(2):128-33.(IF: 1.332)
|
2012 | |
| 599 |
None Explaining anthropometric variations in sickle cell disease requires a multidimensional approach
Indian J Hum Genet. 2012 Jan-Apr;18(1): 1-2.
|
2012 | |
| 600 |
None De novo origin of multiple small supernumerary marker chromosomes (sSMCs) in a child with intellectual disability and dysmorphic features.
Gene. 2012 Apr 25; 498(1):128-30.(IF: 2.443)
|
2012 | |
| 601 |
None MicroRNA profile in understanding pathogenesis of systemic lupus erythematosus
Indian J Biotechnol 2012 Apr; 11:129-33.(IF: 0.55)
|
2012 | |
| 602 |
None Malignancies in Indian haemophiliacs are mainly non viral associated
J Thromb Haemost. 2012 Apr 12.[Epub ahead of print](IF: 5.731)
|
2012 | |
| 603 |
None DNA Copy Number Changes and Immunophenotype Pattern in Karyotypically Normal Acute Myeloid Leukemia Patients from Indian Population.
Genet Test Mol Biomarkers. 2012 Apr;16(4): 265-70.(IF: 1.110)
|
2012 | |
| 604 |
None SRY sequence in maternal plasma: Implications for non-invasive prenatal diagnosis: First report from India
Indian J Hum Genet 2012 Jan-Apr; 18(1): 87-90.
|
2012 | |
| 605 |
None Hemoglobin Lepore Hollandia in India.
Int J Lab Hematol. 2012 Apr;34(2):148-53. (IF: 1.176)
|
2012 | |
| 606 |
None Hemoglobin Showa-Yakushiji: A Common ? Thalassemia Mutation Among the Agri Community from Western India.
Genet Test Mol Biomarkers. 2012 Apr;16(4): 302-5.(IF; 1.110)
|
2012 | |
| 607 |
None Current and emerging therapeutic strategies for Fanconi anemia.
The Hugo J 2012 Mar; 6:1.(IF: )
|
2012 | |
| 608 |
None Heterozygote frequencies of common polymorphic markers of factor VIII (f8) and factor IX (f9) genes in indigenous Nepali population.
Haemophilia. 2012 Mar;18(2):e44-5.(IF: 2.597)
|
2012 | |
| 609 |
None Primary immunodeficiencies in India: a perspective.
Ann N Y Acad Sci. 2012 Feb;1250:73-9.(IF: 3.155)
|
2012 | |
| 610 |
None Is the Poly A (T>C) Mutation a Causative Factor For Misdiagnosis in Second Trimester Prenatal Diagnosis of ?-Thalassemia by Fetal Blood Analysis on High Performance Liquid Chromatography?
Hemoglobin. 2012 Feb; 36(2):114-23. (IF: 1.304)
|
2012 | |
| 611 |
None Clinical Profile of Leukocyte Adhesion Deficiency Type I.
Indian Pediatr 2012 Jan; 49(1): 43-45.(IF:1.048)
|
2012 | |
| 612 |
None A Genome wide search for Non-UGT1A1 markers associated with unconjugated bilirubin levels revelas significant association with a polymorphic marker near a gene of the Nucleoporin family
Ann.Hum.Genet. 2012 Jan; 76(1):33-41.(IF: 2.565)
|
2012 | |
| 613 |
None Homeopathic medicines substantially reduce the need for clotting factor concentrates in haemophilia patients: results of a blinded placebo controlled cross over trial.
Homeopathy. 2012 Jan;101(1):38-43.(IF: 1.141)
|
2012 | |
| 614 |
None Mycobacterium tuberculosis triggers autoimmunity?
Indian J Tuberc. 2012 Jan;59(1):49-51.
|
2012 | |
| 615 |
None Hematologically important mutations: Leukocyte adhesion deficiency (first update)
Blood Cells Mol Dis 2012 Jan 15; 48(1):53-61.(IF: 2.351)
|
2012 | |
| 616 |
None Hla-a and hla-B alleles associated in psoriasis patients from Mumbai, Western India
Indian J Dermatol. 2011 Sep-Oct;56(5):497-500.(IF: 0.979)
|
2011 | |
| 617 |
None Invasive and non-invasive approaches for prenatal diagnosis of haemoglobinopathies: Experiences from India.
Ind. J. Med. Res. 2011 Oct; 134(4): 552-60.(IF: 1.837)
|
2011 | |
| 618 |
None Tuberculosis and female reproductive health.
J Postgrad Med. 2011 Oct-Dec;57(4):307-13.(IF: 1.389)
|
2011 | |
| 619 |
None Incidence of down syndrome: Hypotheses and reality
Indian J Hum Genet. 2011 Sep;17(3):117-9.
|
2011 | |
| 620 |
None HLA-A and HLA-B alleles associated in psoriasis patient’s from Mumbai, Western India
Indian J Dermatol. 2011 Sep-Oct; 56(5): 510-13.(IF: 0.979)
|
2011 | |
| 621 |
None Recent developments in drug resistance mechanism in chronic myeloid leukemia: A review.
Eur J Haematol. 2011 Nov; 87(5):381-93. (IF 2.785)
|
2011 | |
| 622 |
None Mutations in coagulation factor XIII subunit A in severe factor XIII deficiency patients: five novel mutations detected.
Haemophilia. 2011 Sep;17(5):e843-5. (IF 2.597)
|
2011 | |
| 623 |
None A rare case of B-cell chronic lymphocytic leukemia with t(2;14)(p13;q32), +X, +11, +12, +13,+der(1p) karyotype.
Indian J Cancer. 2011 Jul-Sep;48(3):387-8.(IF: 0.961)
|
2011 | |
| 624 |
None HIV and Malaria co-infection in Mumbai Western India.
J Vector Borne Dis. 2011 Sep; 48(3):155-58.(IF: 1.177)
|
2011 | |
| 625 |
None Role of 14-bp deletion/insertion polymorphism in exon 8 of the HLA-G gene in recurrent spontaneous abortion patients.
J Hum Reprod Sci. 2011 Sep;4(3):143-6. (IF:)
|
2011 | |
| 626 |
None Mutations in coagulation factor XIII subunit A in severe factor XIII deficiency patients: five novel mutations detected.
Haemophilia. 2011 Sep;17(5):e843-5.(IF: 2.597)
|
2011 | |
| 627 |
None Haematology research in India: past, present and future
Indian J Hematol Blood Transfus. 2011 Jun;27(2):55-64. (IF: 0.056)
|
2011 | |
| 628 |
None Women scientists in India are marching ahead.
Curr Sci 2011 Aug; 101: 3. (IF: 0.935)
|
2011 | |
| 629 |
None Pathophysiology of acquired von Willebrand disease: a concise review
Eur J Haematol. 2011 Aug;87(2):99-106. Review. (IF 2.785).
|
2011 | |
| 630 |
None Cytogenetic and comparative genomic hybridization study of Indian myelodysplastic syndromes.
Cancer Epidemiol. 2011 Aug;35(4):e1-5.(IF: 2.010)
|
2011 | |
| 631 |
None Fc ? R IIB gene polymorphisms in Indian systemic lupus erythematosus (SLE) patients.
Indian J Med Res. 2011 Aug;134(2):181-5.(IF: 1.837)
|
2011 | |
| 632 |
None Epidemiology, diagnosis, and management of von Willebrand disease in India.
Semin Thromb Hemost. 2011 Jul;37(5):595-601. (IF: 4.524)
|
2011 | |
| 633 |
None Glioma Indian Scenario: Is there a Human Leukocyte Antigen association?
J Nat Sci Biol Med 2011 Jul; 2(2):205-8.
|
2011 | |
| 634 |
None An improved, semi quantitative clot based assay for factor XIII
Haemophilia. 2011 Jul;17(4):718-20. (IF 2.597)
|
2011 | |
| 635 |
None Autoantibody profile and immunological parameters in Recurrent Spontaneous Abortion patients.
Nigerian Med J 2011 Jul; 52(3):163-66.
|
2011 | |
| 636 |
None Response to the letter of Casserta et al. Acquired hemophilia a following influenza vaccination.
Autoimmun Rev. 2011 Jul 23. [Epub ahead of print](IF: 6.624)
|
2011 | |
| 637 |
None Advances in Autoimmune Lymphoproliferative Syndromes (ALPS).
Eur J Haematol. 2011 Jul; 87(1): 1-9. Review (IF 2.785)
|
2011 | |
| 638 |
None Dengue virus infection of SK Hep1 cells: inhibition of in vitro angiogenesis and altered cytomorphology by expressed viral envelope glycoprotein
FEMS Immunol Med Microbiol. 2011 Jul; 62(2):140-7. (IF: 2.441)
|
2011 | |
| 639 |
None CCR5 chemokine receptor polymorphism in patients with HIV-1 from Western India.
J Acquir Immune Defic Syndr. 2011 Jun 1;57(2):e21. (IF: 4.570)
|
2011 | |
| 640 |
None The association between HIV-1 subtype C antiretroviral resistance and HLA prevalence in southern India.
J Acquir Immune Defic Syndr. 2011 May;57(1):e17-19. (IF: 4.570)
|
2011 | |
| 641 |
None Thrombophilic dimension of Budd chiari syndrome and portal venous thrombosis--a concise review.
Thromb Res. 2011 Jun;127(6):505-12. Epub 2010 Oct 20. Review.(IF: 2.44)
|
2011 | |
| 642 |
None Are mannose-binding lectin gene 2 (MBL2) polymorphisms and MBL deficiency associated with infections?
Indian J Hum Genet 2011 May; 17(2):45-47.
|
2011 | |
| 643 |
None Chromosomal aberrations in hematological malignancies: A guide to the identification of novel oncogenes.
Indian J Hum Genet. 2011 May;17(2):43-4
|
2011 | |
| 644 |
None Flow cytometric osmotic fragility-An effective screening approach for red cell membranopathies.
Cytometry Part B Clin Cytom 2011 May; 80(3):186-90.(IF: 2.525)
|
2011 | |
| 645 |
None Deletion of ABL/BCR on der(9) associated with severe basophilia.
Indian J Hum Genet. 2011 May;17(2):100-3.
|
2011 | |
| 646 |
None Human immunodeficiency virus therapeutics and pharmacogenomics.
Indian J Hum Genet. 2011 May;17 Suppl 1:S22-6.
|
2011 | |
| 647 |
None Functional characterization and modified rescue of novel AE1 mutation R730C associated with overhydrated cation leak stomatocytosis
Am J Physiol Cell Physiol 2011 May; 300(5):C1034-C1046.(IF: 3.817)
|
2011 | |
| 648 |
None Acquired hemophilia A: diagnosis, aetiology, clinical spectrum and treatment options.
Autoimmun Rev. 2011 Apr;10(6):311-6. Review.(IF: 6.624)
|
2011 | |
| 649 |
None Association of (GT)n Repeats Promoter Polymorphism of Heme Oxygenase-1 Gene with Serum Bilirubin Levels in Healthy Indian Adults.
Genet Test Mol Biomarkers. 2011 Apr; 15(4):215-18. (IF: 1.110)
|
2011 | |
| 650 |
None Activated partial thromboplastin time reagent: how can a single reagent respond to multiple demands?
Blood Coagul Fibrinolysis. 2011 Apr;22(3):241-2. (IF 1.549)
|
2011 | |
| 651 |
None HLA involvement in nevirapine-induced dermatological reaction in antiretroviral-treated HIV-1 patients.
J Pharmacol Pharmacother. 2011 Apr;2(2):114-5.
|
2011 | |
| 652 |
None Challenges of multiple mutations in individual patients with haemophilia.
Eur J Haematol. 2011 Mar; 86(3): 185-90. (IF 2.785)
|
2011 | |
| 653 |
None Severe mental retardation and recessive congenital methemoglobinemia in three Indian patients: Compound heterozygous for NADH-cytochrome b5 reductase gene mutations.
Am J Hematol. 2011 Mar;86(3):327-9.(IF 3.476).
|
2011 | |
| 654 |
None Involvement of HLA in serum BETA-2 Microglobin levels among Mumbai HIV-1 patients
J Adv Lab Res Biol 2011; I(III):133-35.
|
2011 | |
| 655 |
None Phenotypic diversity of sickle cell disorders: a rebuttal
Curr Sci 2011 Jan; 100(2):149.(IF:0.897)
|
2011 | |
| 656 |
None HLA-B17 Prevalence in HIV-1 infected patients under Antiretroviral treatment.
Int J Hum Genet 2011 Jan; 11(1):59-62.(IF:0.306)
|
2011 | |
| 657 |
None Role of anti-human lymphocyte culture cytotoxic antibodies in recurrent spontaneous pregnancy loss women.
J Hum Reprod Sci. 2011 Jan;4(1):17-9. (IF)
|
2011 | |
| 658 |
None A first case of primary amenorrhea with i(X)(qter---q10::---qter), rob(13;14)(q10;q10), inv(9)(p13q33) karyotype.
J Hum Reprod Sci. 2011 Jan;4(1):53-5. (IF )
|
2011 | |
| 659 |
None Restriction fragmentlength polymorphism (RFLP) of the X chromosome linked glucose-6- phosphate dehydrogenase (G6PD) locus in India.
Ann Hum Biol. 2011 Jan;38(1):106-9.(IF: 1.975)
|
2011 | |
| 660 |
None Molecular characterization of HLA B*07 alleles in HLA B27 negative seronegative spondarthritis patients from India
IUP J Genet Evolution 2011; IV(3):1-8.
|
2011 | |
| 661 |
None Quantitation of HBV DNA; another modification of the test: Will it withstand the test of time?
Indian J Hum Genet. 2011 Jan;17(1):1-2.
|
2011 | |
| 662 |
None Differences in Etiological and Clinical Manifestations in Upper and Lower Limb Deep Venous Thrombosis Patients From India.
Clin Appl Thromb Hemost. 2010 Dec;16(6):698-700.(IF:1.476)
|
2010 | |
| 663 |
None Molecular pathology of haemophilia A in Indian patients: identification of 11 novel mutations.
Clin Chim Acta 2010 Dec 14; 411(23-24):2004-8.(IF:2.661)
|
2010 | |
| 664 |
None Incidence of malignancy and clonal chromosomal abnormalities in Fanconi anemia.
Indian J Cancer. 2010 Oct-Dec;47(4):397-9. (IF: 0.961)
|
2010 | |
| 665 |
None Profiling ?-Thalassaemia mutations in India at state and regional levels: implications genetic education, screening and counseling programmes.
Hugo J. 2009 Dec; 3(1-4): 51–62.
|
2010 | |
| 666 |
None Mannose Binding Lectin (MBL) in Autoimmunity and its role in systemic lupus erythematosus (SLE).
J Assoc Physicians India 2010 Nov; 58(11):688-90.
|
2010 | |
| 667 |
None Double mutations in haemophilia: muddling strangers or indifferent partners in crime?
Haemophilia 2010 Nov;16(6):970-1. (IF 2.394)
|
2010 | |
| 668 |
None The effect of UGT1A1 promoter polymorphism on bilirubin response to hydroxyurea therapy in hemoglobinopathies
Clin Biochem 2010 Nov;43(16-17):1329-1332.(IF: 2.079)
|
2010 | |
| 669 |
None Chromosomal breakage study in children suspected with fanconi anemia in the Indian population.
J Pediatr Hematol Oncol 2010 Nov;32(8):606-10.(IF: 0.998)
|
2010 | |
| 670 |
None Diffuse alveolar haemorrhage with severe haemophilia.
Haemophilia 2010 Nov;16(6): 962-4. (IF 2.394)
|
2010 | |
| 671 |
None Hemolytic anemia and distal renal tubular acidosis in two Indian patients homozygous for SLC4A1/AE1 mutation A858D.
Am J Hematol 2010 Oct;85(10):824-8.(IF 3.576)
|
2010 | |
| 672 |
None Squamous cell carcinoma of tongue in a patient with fanconi’s anemia treated with radiation therapy: Case Report and review of literature.
Head & Neck 2010 Oct;32(10):1422-27.(IF: 2.4)
|
2010 | |
| 673 |
None A descriptive profile of ?-Thalassaemia mutations in India, Pakistan and Sri Lanka
J Community Genet. 2010 Oct 10.
|
2010 | |
| 674 |
None PTPN22 gene polymorphisms in autoimmune diseases with special reference to systemic lupus erythematosus disease susceptibility.
J Postgrad Med. 2010 Jul-Sep;56(3):239-42. Review. (IF:1.389)
|
2010 | |
| 675 |
None Complexities and similarities of HLA antigen distribution in Asian subcontinent.
Indian J Hum Genet. 2010 Sep;16(3):108-10.
|
2010 | |
| 676 |
None Delayed vitamin K deficiency as a cause of bleeding : still a concern in the 21st century!
Blood Coagul Fibrinolysis. 2010 Sept; 21(6):608-10. (IF 1.506)
|
2010 | |
| 677 |
None Clinical, hematologic and molecular variability of sickle cell-? thalassemia in western India
Indian J Hum Genet. 2010 Sep;16(3):154-8.
|
2010 | |
| 678 |
None Sequential serologic testing for common viral markers in blood units in India is probably not cost effective.
Transfusion 2010 Aug;50(8): 1854-55. (IF 3.3)
|
2010 | |
| 679 |
None Protein C (PROC) gene mutations in two Indian families with purpura fulminans
Ann Hematol. 2010 Aug; 89(8): 835-6. (IF: 2.688)
|
2010 | |
| 680 |
None Bachelor of rural health care: cutting the root and watering the stem!
Natl Med J India. 2010 Jul-Aug;23(4):250. (IF 0.541)
|
2010 | |
| 681 |
None JAK2 mutations across a spectrum of venous thrombosis cases.
Am. J. Clin. Pathol 2010 Jul; 134(1):82-5. (IF 2.47)
|
2010 | |
| 682 |
None Molecular basis of factor X deficiency cases from India
Haemophilia 2010 Jul 1; 16(4): 693-7. ( IF 2.394)
|
2010 | |
| 683 |
None Dengue virus-induced autophagosomes and changes in endomembrane ultrastructure
J Electron Microsc (Tokyo). 2010 Jun;59(6):503-11. (IF 1.77)
|
2010 | |
| 684 |
None Advances in Haematological Pharmacotherapy in 21st Century.,
Indian J Hematol Blood Transfus 2010 Apr-Jun; 26(2):30-40.
|
2010 | |
| 685 |
None Epidemiology of beta – thalassemia in Western India:mapping the frequencies and mutations in sub – regions of Maharashtra and Gujarat
Br J Haematol. 2010. Jun; 149(5): 739-47.(IF 4.942)
|
2010 | |
| 686 |
None Human leucocyte antigen class II DRB1 and DQB1 associations in human immunodeficiency virus-infected patients of Mumbai, India
Intl J Immunogenet 2010 Jun; 37(3): 199-204.(IF: 1.62)
|
2010 | |
| 687 |
None Phenotypic heterogeneity and parental origin of extra chromosome 21 in Down Syndrome.
Indian Pediatrics 2010 May 17; 47(5): 429-432. (IF: 0.9)
|
2010 | |
| 688 |
None Integration of modern genetic knowledge and technology into public health in India.
Indian J Hum Genet. 2010 May;16(2):45-6.
|
2010 | |
| 689 |
None Iron deficiency as a risk factor for first febrile seizure.
Indian Pediatr. 2010 May;47(5):437-9. (IF: 0.9)
|
2010 | |
| 690 |
None Fc gamma R IIIBpolymorphisms:their association with clinical manifestation and autoantibodies in SLE patients from western India
Int J Rheum Dis. 2010 May; 13 (2): 138-43.(IF:0.205)
|
2010 | |
| 691 |
None VWF pseudogene; Mimics, masks and spoils.
Clin Chim Acta. 2010 Apr 2;411(7-8):607-9.(IF: 2.661)
|
2010 | |
| 692 |
None Anti-nucleosome antibodies as a disease marker in systemic lupus erythematosus and its correlation with disease activity and other autoantibodies
Indian J Dermatol Venereol Leprol. 2010 Mar-Apr;76(2):145-9.(IF: 0.976)
|
2010 | |
| 693 |
None Frequency of B-thalassemia trait and other hemoglobinopathies in northern and western India.
Indian J Hum Genet. Jan-Apr 2010; 16(1): 16-25.
|
2010 | |
| 694 |
None Association of factor VII gene polymorphisms with Budd Chiari syndrome
Blood Coagul Fibrinolysis. 2010 Apr; 21(3):296-7. (IF 1.506)
|
2010 | |
| 695 |
None Molecular diversity of hemoglobin H disease in India.
Am J Clin Pathol. 2010 Mar;133(3):491-4. (IF 3.576)
|
2010 | |
| 696 |
None Five alpha globin chain variants identified during screening for haemoglobinopathies.
Eur J Clin Invest. 2010 Mar; 40(3):226-32. (IF:2.784)
|
2010 | |
| 697 |
None Modulation of severity of clinical bleeding by co-inherited thrombophilia is also true for severe factor X deficiency
Clin Chim Acta. 2010 Feb;411(3-4):291. (IF:2.960)
|
2010 | |
| 698 |
None Fc ? RIIA Genotypes and Its Association with Anti-C1q Autoantibodies in Lupus Nephritis (LN) Patients from Western India
Autoimmune Dis 2010 Feb 9;2010.
|
2010 | |
| 699 |
None Effect of hydroxyurea on the transfusion requirements in patients with severe HbE-beta-thalassaemia: a genotypic and phenotypic study
J Clin Pathol. 2010 Feb;63(2):147-50. (IF 1.78)
|
2010 | |
| 700 |
None Novel immunophenotypic and morphologic presentation in acute myeloid leukemia (AML) with JAK2 V617F mutation.
Eur J Haematol. 2010 Feb 1;84(2):180-2.(IF:1.478)
|
2010 | |
| 701 |
None Indian Journal of Human Genetics in PubMed: Cautious but confident steps.
Indian J Hum Genet. 2010 Jan;16(1):6-7.
|
2010 | |
| 702 |
None Global burden, distribution and prevention of ?-Thalassemia and hemoglobin E disorders.
Expert Rev. Hematol 2010 Mar, 3(1):103-117.(IF:1.161)
|
2010 | |
| 703 |
None Proteomic approach to autoimmune disorders : A review
Indian J Biotechnol 2010 Jan;9 : 13-7.(IF:--)
|
2010 | |
| 704 |
None The HLA system- A review.
Anthopologist, 2010;Special Vol.6:183-97.
|
2010 | |
| 705 |
None Clinical, Genetic and Cytogenetic study of Fanconi anemia in an Indian population
Hematology 2010 Jan;15(1):58-62. (IF:--) .
|
2010 | |
| 706 |
None Hb H disease due to homozygosity for a rare alpha2-Globin Variant, Hb Sallanches
Hemoglobin 2010 Jan; 34(1): 45-48.(IF:1.106)
|
2010 | |
| 707 |
None Protein C (PROC) gene mutations in two Indian families with purpura fulminans
Ann Hematol. 2010 Jan 14. [Epub ahead of print](IF: 1.496)
|
2010 | |
| 708 |
None ??Thalassemia- What is it ?
Physician’ s Digest 2010; Pg: 63-69.
|
2010 | |
| 709 |
None Exposure to hydroxyurea during pregnancy in sickle ?-thalassemia - A report of 2 cases.
J.Clin. Pharmacol 50; 231-4; 2010.(IF:3.59)
|
2010 | |
| 710 |
None Microsatellite diversity among the primitive tribes of India
Indian J Hum Genet. 2009 Sep-Dec; 15(3): 114-120.
|
2009 | |
| 711 |
None APO-1/Fas gene: Structural and functional characteristics in systemic lupus erythematosus and other autoimmune diseases.
Indian J Hum Genet. 2009 Sep-Dec; 15(3): 98-102.
|
2009 | |
| 712 |
None Private practice in India.
Natl Med J India. 2008 Nov-Dec;21(6):328-9.(IF:0.911)
|
2009 | |
| 713 |
None Familial small supernumerary marker chromosome (sSMC) (14)(:P(11)-q(11):) In a child with translocation down syndrome
Indian J Pediatr. 2009 Dec; 76(12):1265-7. (IF:0.646)
|
2009 | |
| 714 |
None Development of Anti-neutrophil Cytoplasmic antibodies (ANCA) and Vasculitis in BALB/c Mice: A Prototype of human ANCA associated disease.
J. Appl. Anim. Res. 2009 Dec;36:297-302.(IF:0.178)
|
2009 | |
| 715 |
None Comparative case control study of clinical features and human leukocyte antigen susceptibility between familial and nonfamilial vitiligo
Indian J Dermatol Venereol Leprol. 2009 Nov-Dec;75(6):583-7.(IF:0.588)
|
2009 | |
| 716 |
None Association of HLA alleles with hepatitis C infection in Maharashtra, Western India
Indian J Med Res. 2009 Nov;130(5):550-5. (IF: 1.883)
|
2009 | |
| 717 |
None Differences in Etiological and Clinical Manifestations in Upper and Lower Limb Deep Venous Thrombosis Patients From India.
Clin Appl Thromb Hemost. 2009 Nov 10. [Epub ahead of print] (IF: 1.286).
|
2009 | |
| 718 |
None Phenotypic and genotypic characterization of Factor VII deficiency patients from Western India.
Clin Chim Acta. 2009 Nov;409(1-2):106-11.Epub 2009 Sep 13. (IF:2.960)
|
2009 | |
| 719 |
None Cascade screening for ?-thalassemia; A practical approach for identifying and counseling carriers in India.
Indian J. Comm. Med. 2009;Oct 34(4) :354-56.
|
2009 | |
| 720 |
None Molecular heterogeneity of glucose-6-phosphate dehydrogenase deficiency among the tribals in Western India.
Blood Cells Mol Dis. 2009 Sep-Oct;43(2):156-7.(IF: 2.549)
|
2009 | |
| 721 |
None Response to hydroxyurea in beta thalassemia major and intermedia: experience in western India
Clin Chim Acta. 2009 Sep;407(1-2):10-5. (IF:2.960)
|
2009 | |
| 722 |
None Antiphospholipid antibodies in haemophilia patients with severe bleeding tendency cause, consequence or a consequential cause?
Haemophilia. 2009 Sep;15(5):1104-8. (IF 2.394)
|
2009 | |
| 723 |
None Haemophilia care in India: innovations and integrations by various chapters of Haemophilia Federation of India (HFI).
Haemophilia. 2009 Sep 23. [Epub ahead of print] (IF: 2.394)
|
2009 | |
| 724 |
None Iron Deficiency as a Risk Factor for First Febrile Seizure
Indian Pediatr. 2009 Sep 3. [Epub ahead of print](IF:0.956)
|
2009 | |
| 725 |
None Paroxysmal Nocturnal Haemoglobinuria (PNH): diagnostic tests, advantages & limitations.
Eur J Haematol. 2009 Aug ; 83:503-511.(IF 1.478).
|
2009 | |
| 726 |
None Geographical heterogeneity of immigration and career paths of medical graduates in India.
Natl Med J India. 2009 Jul-Aug;22(4):218.(IF:0.911)
|
2009 | |
| 727 |
None Role of HLA class I (HLA-A, B) and HLA class II (HLA-DRB, DQB) in HIV-1 patients with and without pulmonary tuberculosis.
J Acquir Immune Defic Syndr. 2009 Aug 15;51(5):640-1.(IF 4.570)
|
2009 | |
| 728 |
None Monoclonal antibody produced against calf thymus histone.
Hybridoma (Larchmt). 2009 Aug;28(4):277-80.(IF 0.559)
|
2009 | |
| 729 |
None Squamous cell carcinoma of base of tongue in a patient with Fanconi’s anemia treated with radiation therapy: case report and review of literature.
Head & Neck 2009; Aug 11 (E-pub ahead of print)(IF: 2.01).
|
2009 | |
| 730 |
None Cytogenetic study of myelodysplastic syndrome from India.
Indian J Med Res. 2009 Aug;130(2):155-9. (IF: 1.883)
|
2009 | |
| 731 |
None Spectrum of factor IX gene mutations causing haemophilia B from India.
Blood Coagul Fibrinolysis. 2009 Jul; 20(5):333-336.(IF:1.506)
|
2009 | |
| 732 |
None Anti-phospholipid antibodies and other immunological causes of recurrent foetalloss--areview of literature of various therapeutic protocols.
Am J Reprod Immunol. 2009 Jul;62(1):9-24. Review.(IF 2.172)
|
2009 | |
| 733 |
None Challenges of haemophilia care in India: lest we forget.
Indian J Med Res. 2009 Jul;130(1):87-8. (IF 1.883)
|
2009 | |
| 734 |
None HLA B*1502 allele association with oxcarbamazepine-induced skin reactions in epilepsy patient from India.
Epilepsia 2009 Jul; 50(7): 1837-38.(IF:3.733)
|
2009 | |
| 735 |
None Mycobacterium tuberculosis infection precipitates SLE in patients from endemic areas
Rheumatol Int 2009 Jul;29(9):1047-50.(IF:1.327)
|
2009 | |
| 736 |
None Plasminogen activator inhibitor-1 4G/5G gene polymorphism in women with fetal loss.
Int J Gynaecol Obstet. 2009 Jul 21. [Epub ahead of print] (IF: 1.228)
|
2009 | |
| 737 |
None Anti-idiotype antibodies in immune regulation of anca associated vasculitis.
Indian J Dermatol. 2009 Jul;54(3):258-62.
|
2009 | |
| 738 |
None Phenotypic heterogencity and parental origin of extrachromosome 21 in down syndrome.
Indian Pediat. 2009 July 1; [Epub ahead of print] (IF:0.956)
|
2009 | |
| 739 |
None HLA alleles in anti-endothelial cell antibody positive Indian SLE patients
Int J Hum Genet 2009 Apr-Jun; 9(2): 127-30. (IF: Nil)
|
2009 | |
| 740 |
None Regional heterogeneity of beta-thalassemia mutations in the multi ethnic Indian population.
Blood Cells Mol Dis. 2009 May-Jun;42(3):241-6.(IF: 2.549)
|
2009 | |
| 741 |
None The teacher and the taught: medical education in India at the crossroads.
Natl Med J India. 2009 May-Jun:22(3):147-9.(IF:0.911)
|
2009 | |
| 742 |
None Evolution of prenatal diagnostic techniques from phenotypic diagnosis to gene arrays: its likely impact on prenatal diagnosis of hemophilia.
Clin Appl Thromb Hemost. 2009 May-Jun;15(3):277-82. Review. (IF: 1.286)
|
2009 | |
| 743 |
None Double mutations causing haemophilia B: a double whammy!
Br J Haematol. 2009 May;145(3):433-5. (IF: 3.195)
|
2009 | |
| 744 |
None A comparison of the choice of monoclonal antibodies for recovery of fetal cells from maternal blood using FACS for noninvasive prenatal diagnosis of hemoglobinopathies
Cytometry B Clin Cytom. 2009 May 76(B)(3): 175-80. (IF:1.439)
|
2009 | |
| 745 |
None Hereditary basis of protein C deficiency (PCD) in thrombosis patients: First
Thromb Haemost 2009 Apr;101(4):785-87.(IF:3.413)
|
2009 | |
| 746 |
None Absence of Protein C Sapporo in Indian Patients With Venous Thrombosis.
Clin Appl Thromb Hemost. 2009 Apr 28. [Epub ahead of print] (IF: 1.286)
|
2009 | |
| 747 |
None Increased frequency of HLA-B7 among B27 – negative, seronegative spondarthritis patients from Mumbai, Western India.
Br J Biomed Sci 2009 Jan-Mar; 66(1): 25-27.(0.590)
|
2009 | |
| 748 |
None Hematological and molecular analysis of novel and rare beta-thalassemia mutations in the Indian population.
Hemoglobin 2009 Jan-Mar; 33(1):59-65.(IF: 1.106)
|
2009 | |
| 749 |
None Novel mutations in factor IX gene from western India with reference to their phenotypic and haplotypic attributes
J Pediatr Hematol Oncol. 2009 Mar;31(3):157-60.(IF:1.176)
|
2009 | |
| 750 |
None Hydroxyurea in sickle cell disease - A study of clinico-pharmacological efficacy in the Indian haplotype
Blood Cells Mol Dis. 2009 Jan-Feb; 42(1): 25-31.(IF: 2.549)
|
2009 | |
| 751 |
None Novel mutations in GP IIb gene in Glanzmann’s thrombasthenia from India.
Platelets. 2009 Feb;20(1):35-40.(IF: 2.271)
|
2009 | |
| 752 |
None Placental histomorphology in unexplained foetal loss with thrombophilia.
Indian J Med Res 2009 Feb; 129(2): 144-49.(1.883) (IF 1.826)
|
2009 | |
| 753 |
None Spectrum of novel mutations in the human PKLR gene in pyruvate kinase-deficient Indian patients with heterogeneous clinical phenotypes
Clin Genet. 2009 Feb;75(2):157-62.(IF: 3.18)
|
2009 | |
| 754 |
None Murine monoclonal anti-H as typing reagent.
Indian J Med Res 2009 Jan; 129(1): 72-74. (IF: 1.883)
|
2009 | |
| 755 |
None Immune Response to FVIII in Hemophilia A: An Overview of Risk Factors.
Clin Rev Allergy Immunol. 2009 Oct;37(2):58-66. (IF: 2.080)
|
2009 | |
| 756 |
None Antenatal Diagnosis of Thalasssemias-Diagnostic technology suitable for the country
Journal of the Asiatic Society 2009 Vol 51 (2):69-72(IF:--)
|
2009 | |
| 757 |
None HIV-1 evolution drug resistance, and host genetics: The Indian scenario.
Virus Adaption and Treatment 2009; 1:1-4.(IF: open access)
|
2009 | |
| 758 |
None Menorrhagia and reproductive health in rare bleeding disorders: a study from the Indian subcontinent
Haemophilia. 2009 Jan;15(1):199-202. (IF: 2.394)
|
2009 | |
| 759 |
None Molecular evolution of Globin Gene Pathology-Its Driver, Challenges and
Journal of the Asiatic Society 2009 Vol. 51(20):73-8.(IF:--)
|
2009 | |
| 760 |
None Molecular Characterization of ??-Thalassemia and Hereditary Persistence of Fetal Hemoglobin in the Indian Population
Hemoglobin Sep-Oct 2008, Vol. 32, No. 5: 425–433.(IF: 1.00)
|
2008 | |
| 761 |
None Twin pregnancy in a patient of chronic myeloid leukemia on imatinib therapy
Leuk Res 2008 Oct; 32(10) : 1620-2. (IF 2.555)
|
2008 | |
| 762 |
None Evaluation of the Use of Monoclonal Antibodies and Nested PCR for Noninvasive Prenatal Diagnosis of Hemoglobinopathies in India
AJCP Aug 2008; 130(2):202-209.(If: 2.89)
|
2008 | |
| 763 |
None Successful surgery in severe haemophilia – a two stage replacement therapy in resource poor countries.
Haemophilia 2008 Jul 3. (IF 2.394)
|
2008 | |
| 764 |
None antiphospholipid antibodies following tuberculosis lymphadenitis in a predisposed patient.
Blood Coagul Fibrinolysis 2008 Jul;19(5):464-65.[18600102] (IF 1.506)
|
2008 | |
| 765 |
None Reduced clinical severity in a mutationally well – characterized cohort of severe hemophilia with associated thrombophilia
Am. J. Clin Pathol 2008 Jul; 130(1) 84-7. (IF 2.18)
|
2008 | |
| 766 |
None HLA allele associations in idiopathic recurrent spontaneous abortion patients from India.
J. Hum Reprod. Sci, 2008 Jan-Jun;1(1):19-24.
|
2008 | |
| 767 |
None Aspirin resistance in patients with coronary artery disease- which test to use in routine management?
Blood Coagul Fibrinolysis .2008 Jun: 19(4) : 324-6. (IF 1.506)
|
2008 | |
| 768 |
None A novel G143D mutation in the NADH-cytochrome b(5) reductase gene in an Indian patient with type I recessive hereditary methemoglobinemia.
Blood Cells Mol Dis 2008 May-Jun; 40(3):323-7. [17964195] (IF 2.549)
|
2008 | |
| 769 |
None Prevalence and molecular characterization of alpha thalassemia syndromes among Indians
Genet Test. 2008 Jun; 12(2) : 177-80. (IF 1.7)
|
2008 | |
| 770 |
None Imaging the interaction between dengue 2 virus and human blood platelets using atomic force and electron microscopy
J Electron Microsc(Tokyo) 2008 Jun; 57(3):113-8. (IF 1.05)
|
2008 | |
| 771 |
None Carrier screening for ?-thalassemia during pregnancy in India: a 7 year evaluation.
Genet Test. 2008 Jun : 12(2): 181-5. (IF 1.7).
|
2008 | |
| 772 |
None Dengue 2 virus inhibits in vitro megakaryocytic colony formation and induces apoptosis in thrombopoietin-inducible megakaryocytic differentiation from cord blood CD34+ cells.
FEMS Immunol Med Microbiol. 2008 June ; 53 (1):46-51 (IF 2.494)
|
2008 | |
| 773 |
None Hb Showa Yakushi [beta 110(612) Leu?Pro ] in three families from Western India:First report on homozygous Hb showa Yakushiji.
Blood Cells Mol Dis. 2008 May 19. (IF 2.549)
|
2008 | |
| 774 |
None Establishment of a new mismatch PCR-RFLP technique for detection of G10430A common mutation present in moderate to mild haemophilia B patients belonging to Gujarati community from the western part of India.
Haemophilia. 2008 May; 14 (3) : 628-9. (IF 2.394)
|
2008 | |
| 775 |
None A simple, novel and robust test to diagnose type I glanzmann thrombasthenia
Haematologica. 2008 May; 93 (5) :797-8. (IF 6.416)
|
2008 | |
| 776 |
None Successful pregnancy outcome in women with bad obstetric history and recurrent fetal loss due to thrombophilia: effect of unfractionated heparin and low--molecular weight heparin.
Clin Appl Thromb Hemost. 2008 Apr;14(2):174-9. [18160603] (IF 1.286)
|
2008 | |
| 777 |
None Frequency of Partial D in Western India.
Transf Med 2008 Apr; 18(2):91-6.(IF 2.155)
|
2008 | |
| 778 |
None Iron deficiency anaemia in sickle cell disorders in India.
Indian J Med Res 2008 Apr; 127(4):366-9. [18577791](IF 1.826)
|
2008 | |
| 779 |
None A comprehensive screening analysis of antiphospholipid antibodies in Indian women with fetal loss.
Eur J Obstet Gynecol Reprod Biol 2008 Apr;137(2):136-40. (IF 1.736)
|
2008 | |
| 780 |
None Quality and easy availability of medical support overwhelmingly determines the attitude and belief towards genetic testing in haemophilia.
Haemophilia. 2008 Mar;14(2):392-3. [18179571](IF 2.394)
|
2008 | |
| 781 |
None Blood coagulation in falciparum malaria-a review.
Parasitol Res. 2008 Mar;102(4):571-6. [18066597] (IF 3.938)
|
2008 | |
| 782 |
None translocation in a new variant of +(8;21) acute myeloid leukemia involving Xp22.
Indian J Cancer. 2008 Jan-Mar; 45(1):30-2.
|
2008 | |
| 783 |
None Implications of HLA sequence-based typing in transplantation.
J PostGrad Med. 2008 Jan-Mar;54(1):41-4. (IF 1.589)
|
2008 | |
| 784 |
None Background noise of infection for using ANCA as a diagnostic tool for vasculitis in tropical and developing countries.
Parasitol Res. 2008 Apr;102(5):1093-5. Epub 2008 Feb 24. (IF 3.938)
|
2008 | |
| 785 |
None Spontaneous Resolution of Severe Aplastic Anemia following Thymic Hemorrhage
Acta Haematol. 2008 Feb 20;119(2):69-72 (IF 1.316)
|
2008 | |
| 786 |
None A proteomic analysis of CBA-Pk-1slc/Pk-1slc mice with Red Blood Cell Type Pyruvate Kinase deficiency using 2DE together with MALDI-TOF-MF analysis
FASEB J 2008;22:1025. (IF 6.721)
|
2008 | |
| 787 |
None HLA DRB1 alleles in chronic hepatitis B infected patients
Intl J Hum Genet 2008; 72: 275.
|
2008 | |
| 788 |
None An unusual presentation of pediatric acute leukemia
Ind J Hematol Blood Transf 2008; 24:16-22.
|
2008 | |
| 789 |
None Clinical and Laboratory evaluation of idiopathic Male infertility in a secondary referral center in India.
J Clin Lab Analysis 2008; 22: 29-38.
|
2008 | |
| 790 |
None A high cost low volume disease: suitable preventive strategies for developing and developed countries.
The Open Hematol J 2008; 2: 20-4.
|
2008 | |
| 791 |
None Antiendothelial cell antibodies in systemic lupus erytematosus.
Intl J Rheumatol Dis 2008; 11:121-6.(IF 0.205)
|
2008 | |
| 792 |
None Laboratory diagnosis of sickle cell syndrome.
J Community Med 2008 Jan; 4(1): 11-14.
|
2008 | |
| 793 |
None Hemophilia: A High Cost Low Volume Disease:Suitable preventive strategies for developing and developed countries.
The Open Hematology Journal, 2008; 2:20-24.
|
2008 | |
| 794 |
None Amelioration of clinical severity of similar mutations severe factor IX deficiency by coinherited thrombophilia.
Eur J Haematol. 2008 Jan;80(1):87-9. [18028421] (IF 1.478)
|
2008 | |
| 795 |
None A novel R198H mutation in the glucose-6-phosphate dehydrogenase gene in the tribal groups of the Nilgiris in Southern India.
J Hum Genet. 2008;53(2):181-4. [18043863] (IF: 2.431)
|
2008 | |
| 796 |
None Coagulation disorders seen through the window of molecular biology
Ind. J. of Hum Genet. 2007 Sep –Dec; 13(3):79-85. (IF 0.11 )3
|
2007 | |
| 797 |
None Evaluation of F cells in sickle cell disorders by flow cytometry – comparison with theKleihouer- Betke’s slide method
Int J Lab Hematol 2007 Dec: 29 (6): 409-14. (IF 1.304)
|
2007 | |
| 798 |
None Evolution ofprenatal diagnosis techniques from phenotypic diagnosis to gene arrays : Its likely impact on prenatal diagnosis of hemophilia
Clin Appl Thromb Hemost first published on December 26
|
2007 | |
| 799 |
None Strongyloides stercoralis septicaemia following steroid therapy for eosinophilia:report of three cases.
Trans R Soc Trop Med Hyg. 2007 Nov;101(11):1163-5. Epub 2007 Jul 26.(IF 2.615)
|
2007 | |
| 800 |
None Correlation of thromboelastographic patterns with clinical presentation and rationale for use of antifibrinolytics in severe haemophilia patients
Haemophilia
|
2007 | |
| 801 |
None Pathogenesis of anemia in malaria: a concise review
Parasitol Res
|
2007 | |
| 802 |
None MHC non-HLA gene polymorphisms in transplantation
Indian J Pathol Microbiol
|
2007 | |
| 803 |
None Hb Q(India) and its interaction with beta-thalassaemia: a study of 64 cases from India
Br J Biomed Sci
|
2007 | |
| 804 |
None Thalassemia intermedia due to homozygosity for an Asian Indian(Agammadeltabeta) degrees deletional inversion.
Clin Chim Acta. 2007 Oct;385(1-2):81-3. Epub 2007 Jul 19. (IF 2.960)
|
2007 | |
| 805 |
None Glucose-6- phosphate dehydrogenase deficiency and antimalarial drug development.
Am J Trop Med Hyg 2007 Oct;77(4):779-89. Rev. [17978087]. (IF 2.8)
|
2007 | |
| 806 |
None Origin of the Codon 47(+A) ?-thalassemia mutation among the Nicobarese of the Andaman & Nicobar islands in India.
Br J Haematol 2007 Oct;139 (2):345-6. [17897314]. (IF 3.195)
|
2007 | |
| 807 |
None Differentiation of Nijmegen breakage syndrome from Fanconi anemia
Genet Mol Res
|
2007 | |
| 808 |
None Coagulation factor deficiency as a cause of recurrent fetal loss: a red herring!
Blood Coagul Fibrinolysis
|
2007 | |
| 809 |
None Varied distribution of RhD epitopes in the Indian population
Natl Med J India
|
2007 | |
| 810 |
None Contribution of natural anticoagulant and fibrinolytic factors in modulating the clinical severity of haemophilia patients.
Br J Haematol. 2007 Aug;138(4):541-4.(IF 3.195)
|
2007 | |
| 811 |
None Deep venous thrombosis in the antenatal period in a large cohort of pregnancies from western India.
Thromb J. 2007 Jul 4;5:9. (IF 1.0)
|
2007 | |
| 812 |
None HPLC studies in hemoglobinopathies
Indian J Pediatr. 2007 Jul:74(7):657-62 Review. (IF 0.9)
|
2007 | |
| 813 |
None First-trimester prenatal diagnosis of pyruvate kinase deficiency in an Indian family with the pyruvate kinase-Amish mutation
Genet Mol Res
|
2007 | |
| 814 |
None Osteoporosis in young haemophiliacs from western India.
Am J Hematol. 2007 Jun;82(6):453-7. [17278114] (IF 3.576)
|
2007 | |
| 815 |
None Usefulness of prenatal detection of Rh D typing by molecular analysis in Indians
J PostGrad Med. 2007 Apr-Jun; 53(2): 149. (IF 1.589)
|
2007 | |
| 816 |
None Potential of commercial anti-D reagents in the identification of partial D variants in Indian population.
Indian J Med Res. 2007 May;125(5):641-4. [17642499] (IF 1.823)
|
2007 | |
| 817 |
None Previous fetal loss significantly increases the risk of pre-partal deep-vein thrombosis.
Br J Haematol. 2007 Aug;138(4):555-7. [17590183] (IF 3.195)
|
2007 | |
| 818 |
None Fractures of long bones in severe haemophilia.
Haemophilia. 2007 May;13(3):337-9. (IF 2.394).
|
2007 | |
| 819 |
None A common G10430A mutation (Gly 60 Ser) in the factor IX gene presence of moderate and mild hemophilia B in the majority describes the presence of moderate and mild hemophilia B in the majority of the Gujarat population.
Ann Hematol. 2007 May;86(5):377-9. [17308903] (IF 2.688)
|
2007 | |
| 820 |
None 14th International HLA and Immunogenetics Workshop: report from the reproductive immunology component.
Tissue Antigens. 2007 Apr; 69 Suppl 1:297-303. (IF 3.024)
|
2007 | |
| 821 |
None Specific human leukocyte antigen alleles associated with HIV-1 infection in an Indian population.
J Acquir Immune Defic Syndr. 2007 Apr 1;44(4):489-90. [17353719]. (IF 4.262)
|
2007 | |
| 822 |
None Microarray genetic screening: the other side of the coin.
Lancet. 2007 Mar 24;369(9566):992. [17382825] (IF 33.63)
|
2007 | |
| 823 |
None Second trimester antenatal diagnosis in rare coagulation factor deficiencies.
J Pediatr Hematol Oncol. 2007 Mar;29(3):137-9. [17356389] (IF 1.176)
|
2007 | |
| 824 |
None Robustness of factor assays following cordocentesis in the prenatal diagnosis of haemophilia and other bleeding disorders
Haemophilia. 2007 Mar;13(2):172-7. [17286770] (IF 2.394)
|
2007 | |
| 825 |
None G6PD Namoru (208 T C) is the major polymorphic variant in the tribal populations in southern India.
Br J Haematol. 2007 Feb;136(3):512-3. No abstract available. (IF 3.195)
|
2007 | |
| 826 |
None Hyperhomocysteinemia in a cohort of young patients with acute myocardial infarction from Western India: pattern of response to oral folic acid, vitamin B12, B6 therapy
Clin Chim Acta. 2007 Feb;377(1-2):281-2. Epub 2006 Sep 22. (IF 2.960)
|
2007 | |
| 827 |
None Prenatal diagnosis for a novel homozygous mutation in PKLR gene in an Indian family
Prenat Diagn. 2007 Feb; 27(2): 117-8. (IF 2.152)
|
2007 | |
| 828 |
None Optimizing methods of red cell sedimentation from cord blood to maximize nucleated cell recovery prior to cryopreservation
Br J Biomed Sci
|
2007 | |
| 829 |
None Ex vivo expansion of umbilical cord blood stem cells using different combinations of cytokines and stromal cells
Acta Haematol
|
2007 | |
| 830 |
None Fasting plasma homocysteine levels are increased in young patients with acute myocardial infarction from Western India.
Indian Heart J 2007: 59(3):242-5.
|
2007 | |
| 831 |
None Chromosomal breakage in myelodysplatic syndrome.
Asian Pacific J Cancer Preview 2007; 8:151-4. (IF: 1.11)
|
2007 | |
| 832 |
None Human leukocyte antigenpolymorphism and association: a review
Anthropologist 2007;Special Vol. No.3: 367-72.
|
2007 | |
| 833 |
None Dandy – Walker malformation in a case of partial trisomy 9p (p12.1àpter) due to maternal translocation
Indian J Hum Genet 2007;13(1): 33-5.
|
2007 | |
| 834 |
None Assessing the impact of screening and counseling high school children for b-thalassemia in India.
J Med Screen 2007; 14(3): 158. [17925089]. (IF 1.493)
|
2007 | |
| 835 |
None Evaluation of the clinical severity of ?-thalassemia homozygous patients using a phenotypic scoring system
J Chinese Clin Med 2007; 2(8): 439-447
|
2007 | |
| 836 |
None Coagulation disorders seen through the window of molecular biology
Indian J Hum Genet 2007; 13(3) 79-85.
|
2007 | |
| 837 |
None An improved flowcytometric approach for isolation of fetal cells from maternal blood for non invasive prenatal diagnosis of hemoglobinopathies
Hemoglobin, 2007; 31(1): 39-48. (IF 1.106)
|
2007 | |
| 838 |
None HLA association in seronegative spondyloarthritis patients from Mumbai, India.
Int. J Hum Genet. 2007; 7(3): 235-9. (IF 0.238)
|
2007 |
