Published in Thromb Res on January 01, 2003
Role of MTHFR C677T polymorphism in ischemic stroke. Neurol India (2006) 1.60
Leber's hereditary optic neuropathy with molecular characterization in two Indian families. Indian J Ophthalmol (2005) 1.47
Early iron supplementation in very low birth weight infants--a randomized controlled trial. Acta Paediatr (2009) 1.43
Protein C and Protein S: causative factor for developing a hemorrhagic infarct in a HbE/Beta thalassemia child. Indian J Pediatr (2010) 1.39
Prevalence of multiple micronutrient deficiencies amongst pregnant women in a rural area of Haryana. Indian J Pediatr (2004) 1.32
Genetic counseling and prenatal diagnosis in India--experience at Sir Ganga Ram Hospital. Indian J Pediatr (2003) 1.25
Spectrum of haemoglobinopathies diagnosed by cation exchange-HPLC & modulating effects of nutritional deficiency anaemias from north India. Indian J Med Res (2010) 1.22
Effects of dexmedetomidine added to caudal ropivacaine in paediatric lower abdominal surgeries. Indian J Anaesth (2011) 1.20
Tuberculosis in acute leukemia: a clinico-hematological profile. Hematology (2006) 1.14
Pseudo Chediak-Higashi anomaly in acute myelomonocytic leukemia. Indian J Pathol Microbiol (2009) 1.14
Hemoglobin D-Punjab syndromes in India: a single center experience on cation-exchange high performance liquid chromatography. Hematology (2010) 1.12
Ethyl 2-(6-amino-5-cyano-3,4-dimethyl-2H,4H-pyrano[2,3-c]pyrazol-4-yl)acetate. Acta Crystallogr Sect E Struct Rep Online (2010) 1.08
A prospective study of risk factor profile & incidence of deep venous thrombosis among medically-ill hospitalized patients at a tertiary care hospital in northern India. Indian J Med Res (2009) 1.05
Molecular characterization of hemoglobin D Punjab traits and clinical-hematological profile of the patients. Sao Paulo Med J (2012) 1.04
Past, present & future scenario of thalassaemic care & control in India. Indian J Med Res (2011) 1.01
Protein C system defects in Indian children with thrombosis. Ann Hematol (2004) 0.99
Factor V Leiden--the commonest molecular defect in arterial and venous thrombophilia in India. Thromb Res (2003) 0.98
Inherited prothrombotic defects in Budd-Chiari syndrome and portal vein thrombosis: a study from North India. Am J Clin Pathol (2004) 0.97
Cryptococcal neoformans profiles in peripheral blood neutrophils: an unusual presentation. Indian J Pathol Microbiol (2008) 0.95
β-Thalassemia mutations in subjects with borderline HbA₂ values: a pilot study in North India. Clin Chem Lab Med (2011) 0.93
Neonatal thrombosis. Indian J Pediatr (2003) 0.93
Identification of 32 novel mutations in the factor VIII gene in Indian patients with hemophilia A. Haematologica (2005) 0.93
Comparison of HemoCue method with the cyanmethemoglobin method for estimation of hemoglobin. Indian Pediatr (2003) 0.93
Intracranial hemorrhage in childhood immune thrombocytopenic purpura. Pediatr Blood Cancer (2009) 0.91
Novel pyrazole-3-carboxamide derivatives as cannabinoid-1 (CB1) antagonists: journey from non-polar to polar amides. Bioorg Med Chem Lett (2010) 0.90
Acute promyelocytic leukemia with secondary myelofibrosis -- case report and review of the literature. Am J Hematol (2006) 0.89
The therapeutic effect of bone marrow-derived liver cells in the phenotypic correction of murine hemophilia A. Blood (2009) 0.89
Hydroxyurea in thalassemia intermedia--a promising therapy. Ann Hematol (2005) 0.89
Carrier detection in Glanzmann thrombasthenia: comparison of flow cytometry and Western blot with respect to DNA mutation. Am J Clin Pathol (2008) 0.89
Daily versus intermittent iron supplementation in pregnant women: hematological and pregnancy outcome. J Obstet Gynaecol Res (2004) 0.89
Ultrastructural studies on the neuromuscular control of human tracheal and bronchial muscle. Respir Physiol (1986) 0.89
Inhibition of TFG function causes hereditary axon degeneration by impairing endoplasmic reticulum structure. Proc Natl Acad Sci U S A (2013) 0.89
Cytogenetic profile of Indian patients with de novo myelodysplastic syndromes. Indian J Med Res (2011) 0.89
Variability in CYP2C9 allele frequency: a pilot study of its predicted impact on warfarin response among healthy South and North Indians. Pharmacol Rep (2013) 0.88
Clopidogrel resistance in North Indian patients of coronary artery disease and lack of its association with platelet ADP receptors P2Y1 and P2Y12 gene polymorphisms. Platelets (2012) 0.88
Prothrombotic factors and the risk of acute onset non-cardioembolic stroke in young Asian Indians. Thromb Res (2009) 0.88
A novel thromboelastographic score to identify overt disseminated intravascular coagulation resulting in a hypocoagulable state. Am J Clin Pathol (2010) 0.88
Roles of protein C, protein S, and antithrombin III in acute leukemia. Am J Hematol (2006) 0.88
Pharmacogenetic typing for oral anti-coagulant response among factor V Leiden mutation carriers. Indian J Hum Genet (2012) 0.87
Spectrum of inherited bleeding disorders in Indians. Clin Appl Thromb Hemost (2005) 0.87
Inherited platelet function disorders versus other inherited bleeding disorders: an Indian overview. Thromb Res (2007) 0.87
HFE mutation H63D predicts risk of iron over load in thalassemia intermedia irrespective of blood transfusions. Indian J Pathol Microbiol (2007) 0.86
Plasminogen activator inhibitor-1 (PAI-1) gene 4G/5G promoter polymorphism is seen in higher frequency in the Indian patients with deep vein thrombosis. Clin Appl Thromb Hemost (2009) 0.86
Phenotypic and molecular characterisation of type 3 von Willebrand disease in a cohort of Indian patients. Thromb Haemost (2013) 0.86
Glanzmann's thrombasthenia: an overview. Clin Appl Thromb Hemost (2008) 0.86
Five novel mutations in tyrosinase gene of Japanese and Indian patients with oculocutaneous albinism type I (OCA1). J Invest Dermatol (2005) 0.86
Status of serum ferritin and folate levels amongst young women in a rural community of Haryana, India. Nepal Med Coll J (2004) 0.86
Use of ethnicity-specific sequence tag site markers for Y chromosome microdeletion studies. Genet Test Mol Biomarkers (2011) 0.86
Regulatory T cells: a review. Natl Med J India (2013) 0.85
Clinical profile of dengue infection in patients with hematological diseases. Mediterr J Hematol Infect Dis (2011) 0.85
6,8-Dichloro-N-methyl-3-nitro-4-nitro-methyl-4H-chromen-2-amine. Acta Crystallogr Sect E Struct Rep Online (2011) 0.85
Disseminated intravascular coagulation as an unusual presentation of Kala-azar: report of two cases. Scand J Infect Dis (2004) 0.85
Recurrent abortions in Asian Indians: no role of factor V Leiden Hong Kong/Cambridge mutation and MTHFR polymorphism. Clin Appl Thromb Hemost (2007) 0.85
Homocystine levels, polymorphisms and the risk of ischemic stroke in young Asian Indians. J Stroke Cerebrovasc Dis (2009) 0.85
Bone marrow aplasia--a rare complication of imatinib therapy in CML patients. Am J Hematol (2007) 0.85
Haematological & molecular profile of acute myelogenous leukaemia in India. Indian J Med Res (2009) 0.85
Prothrombotic polymorphisms, mutations, and their association with pediatric non-cardioembolic stroke in Asian-Indian patients. Ann Hematol (2008) 0.85
Prevalence of JAK2 V617F mutation in Indian patients with chronic myeloproliferative disorders. Indian J Med Res (2010) 0.84
6-Amino-3,4-dimethyl-4-phenyl-2H,4H-pyrano[2,3-c]pyrazole-5-carbonitrile. Acta Crystallogr Sect E Struct Rep Online (2011) 0.84
Glutathione S-transferase gene deletions and their effect on iron status in HbE/beta thalassemia patients. Ann Hematol (2009) 0.84
The clinico-hematological profile of hairy cell leukaemia: a single centre experience. Hematology (2010) 0.84
Multicenter study of the molecular basis of thalassemia intermedia in different ethnic populations. Hemoglobin (2007) 0.84
Transformation of myelodysplastic syndrome to T-cell acute lymphoblastic leukemia in a young adult. Pediatr Hematol Oncol (2009) 0.84
Sero-entomological investigations on Japanese encephalitis outbreak in Gorakhpur division, Uttar Pradesh, India. Indian J Med Res (2009) 0.83
Thirty-nine cases of pure red cell aplasia: a single center experience from India. Hematology (2007) 0.83
Coagulation factor V gene analysis in five Indian patients: identification of three novel small deletions. Haematologica (2006) 0.83
B cell suppression in newborn following treatment of pregnant diffuse large B-cell lymphoma patient with rituximab containing regimen. Indian J Pediatr (2014) 0.82
Acquired von Willebrand's disease associated with gastrointestinal angiodysplasia: a case report. Haemophilia (2006) 0.82
Comparison of effect of daily versus weekly iron supplementation during pregnancy on lipid peroxidation. J Obstet Gynaecol Res (2009) 0.82
Genotypic influence of α-deletions on the phenotype of Indian sickle cell anemia patients. Korean J Hematol (2011) 0.82
Factor V Leiden: is it the chief contributor to activated protein C resistance in Asian-Indian patients with deep vein thrombosis? Clin Chim Acta (2008) 0.82
An update on the prevalence and characterization of H-PF4 antibodies in Asian-Indian patients. Semin Thromb Hemost (2009) 0.82
Characterisation of mutations and molecular studies of type 2 von Willebrand disease. Thromb Haemost (2012) 0.82
Trigonelline and diosgenin attenuate ER stress, oxidative stress-mediated damage in pancreas and enhance adipose tissue PPARγ activity in type 2 diabetic rats. Mol Cell Biochem (2014) 0.82
Do parental perceptions and motivations towards genetic testing and prenatal diagnosis for deafness vary in different cultures? Am J Med Genet A (2012) 0.81
Characterization and cell material interactions of PEGylated PNIPAAM nanoparticles. Colloids Surf B Biointerfaces (2010) 0.81
Venous thrombosis: prevalence of prothrombotic defects in north Indian population. Indian J Pathol Microbiol (2003) 0.81
Disseminated intravascular coagulation in acute leukemia at presentation and during induction therapy. Clin Appl Thromb Hemost (2007) 0.81
Mutation reports: intron 1 and 22 inversions in Indian haemophilics. Ann Hematol (2003) 0.81
The nitric oxide synthase 3 gene polymorphisms and their association with deep vein thrombosis in Asian Indian patients. Clin Chim Acta (2010) 0.81
Prevalence of Myrsidea salimalii (Amblycera: Phthiraptera) on striated babblers (Turdoides earlei) (Timaliidae: Passeriformes: Aves). J Parasit Dis (2011) 0.81
Cord blood analysis for prenatal diagnosis of thalassemia major and hemophilia A. Indian Pediatr (2005) 0.81
Molecular diagnosis of infantile Neuro axonal Dystrophy by Next Generation Sequencing. Indian J Pediatr (2014) 0.81
Transient leukemia. Indian J Pathol Microbiol (2009) 0.81
Erythroleukemia: a clinco-hematological review of four cases. Indian Pediatr (2004) 0.80
Prenatal diagnosis of haemophilia A by chorionic villus sampling and cordocentesis: all India Institute of Medical Science experience. Vox Sang (2007) 0.80
Establishing a normal reference range for thromboelastography in North Indian healthy volunteers. Indian J Pathol Microbiol (2014) 0.80
Carrier detection in severe von Willebrand's disease. Ann Hematol (2004) 0.80
Priapism: an unusual manifestation of warfarin-induced skin necrosis with protein C deficiency. J Assoc Physicians India (2006) 0.80
Clinico-hematologic profile of factor XIII-deficient patients. Clin Appl Thromb Hemost (2005) 0.80
Impact of FLT3 internal tandem duplications on Indian acute promyelocytic leukemia patients: prognostic implications. Hematology (2007) 0.80
Gene conversions are a common cause of von Willebrand disease. Br J Haematol (2005) 0.80
Conformational change of UGT1A1 by a novel missense mutation (p.L131P) causing Crigler-Najjar syndrome type I. J Pediatr Gastroenterol Nutr (2008) 0.80
Molecular Diagnosis of Hereditary Fructose Intolerance: Founder Mutation in a Community from India. JIMD Rep (2015) 0.80