Published in Clin Chim Acta on January 07, 2010
Epidemiology of beta-thalassaemia in Western India: mapping the frequencies and mutations in sub-regions of Maharashtra and Gujarat. Br J Haematol (2010) 2.12
Acquired hemophilia a: diagnosis, aetiology, clinical spectrum and treatment options. Autoimmun Rev (2010) 1.90
Hereditary thrombophilia in cerebral venous thrombosis: a study from India. Blood Coagul Fibrinolysis (2013) 1.66
Combination of thrombophilia markers in acute myocardial infarction of the young. Indian J Med Sci (2004) 1.52
Bone health in persons with haemophilia: a review. Eur J Haematol (2012) 1.44
Efficacy of fixed low dose hydroxyurea in Indian children with sickle cell anemia: a single centre experience. Indian Pediatr (2013) 1.44
Hydroxyurea in sickle cell disease--a study of clinico-pharmacological efficacy in the Indian haplotype. Blood Cells Mol Dis (2008) 1.43
Prevalence and spectrum of von Willebrand disease from western India. Indian J Med Res (2005) 1.43
Antihistone and other autoantibodies in beta-thalassemia major patients receiving iron chelators. Acta Haematol (2003) 1.40
Mitochondrial DNA variations in myelodysplastic syndrome. Ann Hematol (2013) 1.39
Matrix metalloproteinase and its drug targets therapy in solid and hematological malignancies: an overview. Mutat Res (2013) 1.17
Prevalence and molecular characterization of alpha-thalassemia syndromes among Indians. Genet Test (2008) 1.16
Tuberculosis and immune thrombocytopenia. Haematologica (2002) 1.15
Thrombophilic dimension of Budd chiari syndrome and portal venous thrombosis--a concise review. Thromb Res (2010) 1.10
Response to hydroxyurea in beta thalassemia major and intermedia: experience in western India. Clin Chim Acta (2009) 1.09
Immune response to FVIII in hemophilia A: an overview of risk factors. Clin Rev Allergy Immunol (2009) 1.08
Fasting plasma homocysteine levels are increased in young patients with acute myocardial infarction from Western India. Indian Heart J (2009) 1.08
Regional heterogeneity of beta-thalassemia mutations in the multi ethnic Indian population. Blood Cells Mol Dis (2009) 1.08
Potential of commercial anti-D reagents in the identification of partial D variants in Indian population. Indian J Med Res (2007) 1.07
Newborn screening shows a high incidence of sickle cell anemia in Central India. Hemoglobin (2012) 1.04
First-trimester prenatal diagnosis in haemophilia A and B families--10 years experience from a centre in India. Prenat Diagn (2006) 1.03
Glanzmann's thrombasthenia: updated. Platelets (2002) 1.03
Clinical, hematologic and molecular variability of sickle cell-β thalassemia in western India. Indian J Hum Genet (2010) 1.03
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) 0.99
Low-Molecular-Weight Heparin for Women With Unexplained Recurrent Pregnancy Loss. Ann Intern Med (2015) 0.98
Strongyloides stercoralis septicaemia following steroid therapy for eosinophilia: report of three cases. Trans R Soc Trop Med Hyg (2007) 0.98
Blood coagulation in falciparum malaria--a review. Parasitol Res (2007) 0.98
Osteoporosis in young haemophiliacs from western India. Am J Hematol (2007) 0.96
A simple diagnostic strategy for RhD typing in discrepant cases in the Indian population. Blood Transfus (2012) 0.95
Contribution of natural anticoagulant and fibrinolytic factors in modulating the clinical severity of haemophilia patients. Br J Haematol (2007) 0.95
Influence of CYP2C9 and VKORC1 gene polymorphisms on warfarin dosage, over anticoagulation and other adverse outcomes in Indian population. Eur J Pharmacol (2013) 0.94
Beta-globin gene cluster haplotypes linked to the betaS gene in western India. Hemoglobin (2004) 0.93
Cause of deep venous thrombosis and pulmonary embolism in young patients from India as compared with other ethnic groups. Blood Coagul Fibrinolysis (2012) 0.92
Congenital methemoglobinemia caused by Hb-MRatnagiri (beta-63CAT-->TAT, His-->Tyr) in an Indian family. Am J Hematol (2005) 0.92
Mutations in the MCFD2 gene and a novel mutation in the LMAN1 gene in Indian families with combined deficiency of factor V and VIII. Am J Hematol (2005) 0.92
Anti-phospholipid antibodies and other immunological causes of recurrent foetal loss--a review of literature of various therapeutic protocols. Am J Reprod Immunol (2009) 0.91
Hereditary protein C deficiency in Indian patients with venous thrombosis. Ann Hematol (2012) 0.91
Mannose binding lectin (MBL) in autoimmunity and its role in systemic lupus erythematosus (SLE). J Assoc Physicians India (2010) 0.91
Effect of hydroxyurea on the transfusion requirements in patients with severe HbE-beta-thalassaemia: a genotypic and phenotypic study. J Clin Pathol (2010) 0.90
Molecular diversity of hemoglobin H disease in India. Am J Clin Pathol (2010) 0.89
Immune-mediated thrombocytopenia following dactinomycin therapy in a child with alveolar rhabdomyosarcoma: the unresolved issues. J Pediatr Hematol Oncol (2004) 0.89
Deep venous thrombosis in the antenatal period in a large cohort of pregnancies from western India. Thromb J (2007) 0.89
HLA A*02 allele frequencies and B haplotype associations in Western Indians. Hum Immunol (2003) 0.89
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 (2007) 0.88
Human platelet specific antigens and their importance. Indian Pediatr (2004) 0.88
Paroxysmal nocturnal haemoglobinuria: diagnostic tests, advantages, & limitations. Eur J Haematol (2009) 0.88
JAK2 mutations across a spectrum of venous thrombosis cases. Am J Clin Pathol (2010) 0.87
Sickle cell disease in India. Curr Opin Hematol (2014) 0.87
Advances in autoimmune lymphoproliferative syndromes. Eur J Haematol (2011) 0.87
Variable phenotypes of sickle cell disease in India with the Arab-Indian haplotype. Br J Haematol (2014) 0.85
Splenic function in Omani children with sickle cell disease: correlation with severity index, hemoglobin phenotype, iron status, and alpha-thalassemia trait. Pediatr Hematol Oncol (2002) 0.85
Chromosomal breakage study in children suspected with Fanconi anemia in the Indian population. J Pediatr Hematol Oncol (2010) 0.85
An unusual presentation of pediatric acute lymphoblastic leukemia. Indian J Hematol Blood Transfus (2008) 0.85
Pathophysiology of acquired von Willebrand disease: a concise review. Eur J Haematol (2011) 0.85
Hb H disease due to homozygosity for a rare alpha2-globin variant, Hb Sallanches. Hemoglobin (2010) 0.85
Glucose-6-phosphate dehydrogenase (G6PD) deficiency among tribal populations of India - Country scenario. Indian J Med Res (2015) 0.85
Autoimmune lymphoproliferative syndrome caused by a homozygous null FAS ligand (FASLG) mutation. J Allergy Clin Immunol (2012) 0.84
Hemoglobin Fontainebleau [a21(B2)Ala>Pro]: The second report from India. Indian J Hum Genet (2013) 0.84
Letter: HLA B*1502 allele association with oxcarbamazepine-induced skin reactions in epilepsy patient from India. Epilepsia (2009) 0.84
Chronic synovitis and HLA B27 in patients with severe haemophilia. Lancet (2003) 0.84
Sickle cell disease in tribal populations in India. Indian J Med Res (2015) 0.84
Imaging the interaction between dengue 2 virus and human blood platelets using atomic force and electron microscopy. J Electron Microsc (Tokyo) (2008) 0.84
Elevated procoagulant endothelial and tissue factor expressing microparticles in women with recurrent pregnancy loss. PLoS One (2013) 0.83
Novel immunophenotypic and morphologic presentation in acute myeloid leukemia (AML) with JAK2 V617F mutation. Eur J Haematol (2009) 0.83
Identification of a novel large intragenic deletion in a family with Fanconi anemia: first molecular report from India and review of literature. Gene (2013) 0.83
Thrombophilic dimension of recurrent fetal loss in Indian patients. Blood Coagul Fibrinolysis (2008) 0.83
Recent developments in drug resistance mechanism in chronic myeloid leukemia: a review. Eur J Haematol (2011) 0.83
Novel mutations in GP IIb gene in Glanzmann's thrombasthenia from India. Platelets (2009) 0.82
Dandy-Walker malformations in a case of partial trisomy 9p (p12.1→pter) due to maternal translocation t(9;12)(p12.1;p13.3). Indian J Hum Genet (2007) 0.82
The spectrum of bleeding disorders in women with menorrhagia: a report from Western India. Ann Hematol (2004) 0.82
A common founder mutation p.P2063S in exon 36 of VWF in 11 unrelated Indian von Willebrand disease (VWD) families. Ann Hematol (2013) 0.82
Defining the allelic variants of HLA A19 in the western Indian population. Hum Immunol (2002) 0.82
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) 0.81
An atypical manifestation of acquired von Willebrand syndrome (AVWS) associated with systemic lupus erythematosus (SLE). Ann Hematol (2013) 0.81
A comprehensive screening analysis of antiphospholipid antibodies in Indian women with fetal loss. Eur J Obstet Gynecol Reprod Biol (2007) 0.81
Neuropsychiatric manifestations and associated autoantibodies in systemic lupus erythematosus patients from Western India. Rheumatol Int (2014) 0.81
Ex vivo expansion of umbilical cord blood stem cells using different combinations of cytokines and stromal cells. Acta Haematol (2007) 0.81
Sickle cell disease in India: A perspective. Indian J Med Res (2016) 0.80
Molecular heterogeneity of glucose-6-phosphate dehydrogenase deficiency among the tribals in Western India. Blood Cells Mol Dis (2009) 0.80
Human platelet alloantigen polymorphism in Glanzmann's thrombasthenia and its impact on the severity of the disease. Br J Haematol (2002) 0.80