Best 10 Publications of NIIH from Mar 2012 to Apr 2013.
Pai N, Ghosh K, Shetty S. Hereditary protein C deficiency in Indian patients with venous thrombosis.
Ann Hematol . 2012Sep;91(9):1471-6.(IF: 2.615)
Warang P, Kedar P, Ghosh K, Colah R. 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)
Lobo V, Shetty S, Kulkarni B, Ghosh K. A novel ELISA for diagnosis of Glanzmann's thrombasthenia and the heterozygote carriers. Ann Hematol . 2012 Jun; 91(6):917-21.(IF: 2.615)
Kulkarni S, K Vasantha, Ghosh K A simple diagnostic strategy for RhD typing in discrepant cases in the Indian population. Blood Transfus 2012 Jul; 12: 1-6. (IF: 2.099)
Upadhye DS, Jain D, Nair SB, Nadkarni AH, Ghosh K, Colah RB. First case of Hb Fontainebleau with sickle haemoglobin and other non-deletional α gene variants identified in neonates during newborn screening for sickle cell disorders. J Clin Pathol . 2012 Jul;65(7):654-9.(IF: 2.306)
Italia K, Sawant P, Surve R, Wadia M, Nadkarni A, Ghosh K, Colah R. Variable haematological and clinical presentation of β-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)
Pinto P, Ghosh K, Shetty S. 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)
Colaco S, Colah R, Ghosh K, Nadkarni A. 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)
Ghosh K , Swaminathan S, Madkaikar M, Gupta M, Kerketta L, Vundinti B. 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)
Magerus-Chatinet A, Stolzenberg MC, Lanzarotti N, Neven B, Daussy C, Picard C, Neveux N, Desai M, Rao M, Ghosh K, Madkaikar M, Fischer A, Rieux-Laucat F. 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)