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COVID‐19 and preeclampsia: The unique and the mutually nonexclusive clinical manifestations.
- Published in:
- American Journal of Reproductive Immunology, 2023, v. 89, n. 5, p. 1, doi. 10.1111/aji.13700
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- Publication type:
- Article
Low dose emicizumab prophylaxis in haemophilia a patients: A pilot study from India.
- Published in:
- Haemophilia, 2023, v. 29, n. 3, p. 931, doi. 10.1111/hae.14785
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- Publication type:
- Article
Low‐dose prophylaxis and its impact on the health of haemophilia patients.
- Published in:
- Vox Sanguinis, 2022, v. 117, n. 7, p. 900, doi. 10.1111/vox.13278
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- Publication type:
- Article
Novel RASGRP2 variants in platelet function defects: Indian study.
- Published in:
- British Journal of Haematology, 2022, v. 197, n. 3, p. 377, doi. 10.1111/bjh.18049
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- Publication type:
- Article
A rare case of Glanzmann's thrombasthenia and factor VII deficiency due to a combination of pathogenic and non‐pathogenic gene variants.
- Published in:
- Haemophilia, 2020, v. 26, n. 1, p. e26, doi. 10.1111/hae.13898
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- Publication type:
- Article
A rare cause of bleeding in two Indian families with congenital alpha‐2‐antiplasmin deficiency.
- Published in:
- Haemophilia, 2019, v. 25, n. 6, p. e370, doi. 10.1111/hae.13851
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- Publication type:
- Article
Warfarin Dose Model for the Prediction of Stable Maintenance Dose in Indian Patients.
- Published in:
- Clinical & Applied Thrombosis/Hemostasis, 2018, v. 24, n. 2, p. 353, doi. 10.1177/1076029616683046
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- Publication type:
- Article
A possible need for routine screening for Strongyloides stercoralis infection in Indian haemophilia patients.
- Published in:
- Indian Journal of Medical Research, 2018, v. 147, n. 3, p. 315, doi. 10.4103/ijmr.IJMR_1236_16
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- Publication type:
- Article
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.
- Published in:
- 2017
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- Publication type:
- case study
Investigation of Plasminogen Activator Inhibitor-1 ( PAI-1) 4G/5G promoter polymorphism in Indian venous thrombosis patients: A case-control study.
- Published in:
- European Journal of Haematology, 2017, v. 99, n. 3, p. 249, doi. 10.1111/ejh.12912
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- Publication type:
- Article
Indian Bombay phenotype: it is different!
- Published in:
- Blood Transfusion (17232007), 2017, v. 15, n. 1, p. 74, doi. 10.2450/2016.0266-15
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- Publication type:
- Article
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.
- Published in:
- 2016
- By:
- Publication type:
- letter
Factor VIII Antigen, Activity, and Mutations in Hemophilia A.
- Published in:
- Clinical & Applied Thrombosis/Hemostasis, 2016, v. 22, n. 4, p. 381, doi. 10.1177/1076029614562951
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- Publication type:
- Article
A simple clot based assay for detection of procoagulant cell-derived microparticles.
- Published in:
- Clinical Chemistry & Laboratory Medicine, 2016, v. 54, n. 5, p. 799, doi. 10.1515/cclm-2015-0508
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- Publication type:
- Article
Possible selection of host folate pathway gene polymorphisms in patients with malaria from a malaria endemic region in North East India.
- Published in:
- Transactions of the Royal Society of Tropical Medicine & Hygiene, 2016, v. 110, n. 5, p. 294, doi. 10.1093/trstmh/trw026
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- Publication type:
- Article
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 influencing fetal growth.
- Published in:
- 2016
- By:
- Publication type:
- letter
Decrease in circulating percentage platelet microparticles during pregnancy-a different perspective.
- Published in:
- 2016
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- Publication type:
- journal article
Effect of anticoagulant therapy on cell-derived microparticles and pregnancy outcome in women with pregnancy loss.
- Published in:
- British Journal of Haematology, 2015, v. 171, n. 5, p. 892, doi. 10.1111/bjh.13460
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- Publication type:
- Article
Additional markers for genetic diagnosis of type 3 von Willebrand disease in Indian population.
- Published in:
- Indian Journal of Medical Research, 2015, v. 142, n. 6, p. 759, doi. 10.4103/0971-5916.174570
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- Publication type:
- Article
Low-Molecular-Weight Heparin for Women With Unexplained Recurrent Pregnancy Loss.
- Published in:
- 2015
- By:
- Publication type:
- journal article
Sense, missense, and nonsense: a novel mechanism of premature termination codon (PTC) mutation in a severe von Willebrand disease (VWD) patient.
- Published in:
- 2015
- By:
- Publication type:
- Letter
Erratum to: A novel ELISA for diagnosis of Glanzmann's thrombasthenia and the heterozygote carriers.
- Published in:
- 2015
- By:
- Publication type:
- Erratum
High heterozygosity frequency of three exonic SNPs of factor V gene (F5): implications for genetic diagnosis.
- Published in:
- Indian Journal of Medical Research, 2015, v. 142, n. 1, p. 85, doi. 10.4103/0971-5916.162130
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- Publication type:
- Article
Paradoxical Bleeding and Thrombosis in a Patient With Afibrinogenemia and Fibrinogen Mumbai Mutation.
- Published in:
- American Journal of Clinical Pathology, 2015, v. 143, n. 5, p. 755, doi. 10.1309/AJCPDQL7LXMY7SHW
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- Publication type:
- Article
Nanoimaging in cardiovascular diseases: Current state of the art.
- Published in:
- Indian Journal of Medical Research, 2015, v. 141, n. 3, p. 285, doi. 10.4103/0971-5916.156557
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- Publication type:
- Article
Molecular Pathology of Rare Bleeding Disorders (RBDs) in India: A Systematic Review.
- Published in:
- PLoS ONE, 2014, v. 9, n. 10, p. 1, doi. 10.1371/journal.pone.0108683
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- Publication type:
- Article
Acquired and Heritable Thrombophilia in Indian Patients With Pediatric Deep Venous Thrombosis (DVT).
- Published in:
- Clinical & Applied Thrombosis/Hemostasis, 2014, v. 20, n. 6, p. 573, doi. 10.1177/1076029613476339
- By:
- Publication type:
- Article
Mutations in Intron 1 and Intron 22 Inversion Negative Haemophilia A Patients from Western India.
- Published in:
- PLoS ONE, 2014, v. 9, n. 5, p. 1, doi. 10.1371/journal.pone.0097337
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- Publication type:
- Article
Prenatal diagnosis in severe von Willebrand disease families from India using combination of phenotypic and genotypic assays.
- Published in:
- Prenatal Diagnosis, 2014, v. 34, n. 4, p. 377, doi. 10.1002/pd.4315
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- Publication type:
- Article
Novel genetic abnormalities in Bernard-Soulier syndrome in India.
- Published in:
- Annals of Hematology, 2014, v. 93, n. 3, p. 381, doi. 10.1007/s00277-013-1895-x
- By:
- Publication type:
- Article
A specific and sensitive activated partial thromboplastin time (APTT)-based factor VIII inhibitor screening assay.
- Published in:
- Clinical Chemistry & Laboratory Medicine, 2014, v. 52, n. 3, p. e39, doi. 10.1515/cclm-2013-0595
- By:
- Publication type:
- Article
Delayed Vitamin K Deficiency Related Bleeding: Is it Genetically Linked?
- Published in:
- 2014
- By:
- Publication type:
- Letter
Genetic Heterogeneity in a Large Cohort of Indian Type 3 von Willebrand Disease Patients.
- Published in:
- PLoS ONE, 2014, v. 9, n. 3, p. 1, doi. 10.1371/journal.pone.0092575
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- Publication type:
- Article
An atypical manifestation of acquired von Willebrand syndrome (AVWS) associated with systemic lupus erythematosus (SLE).
- Published in:
- 2014
- By:
- Publication type:
- Letter
An atypical manifestation of acquired von Willebrand syndrome (AVWS) associated with systemic lupus erythematosus (SLE)
- Published in:
- 2014
- By:
- Publication type:
- Journal Article
Elevated Procoagulant Endothelial and Tissue Factor Expressing Microparticles in Women with Recurrent Pregnancy Loss.
- Published in:
- PLoS ONE, 2013, v. 8, n. 11, p. 1, doi. 10.1371/journal.pone.0081407
- By:
- Publication type:
- Article
A common founder mutation p.P2063S in exon 36 of VWF in 11 unrelated Indian von Willebrand disease (VWD) families.
- Published in:
- 2013
- By:
- Publication type:
- Letter
Factor VIII haplotypes in severe hemophilia A patients in India.
- Published in:
- 2013
- By:
- Publication type:
- Letter
Prevalence of factor V G1691A, factor II G20210A, methylenetetrahydrofolate reaductase C677T and endothelial protein C receptor 23 bp insertion polymorphisms in indigenous population of Nepal.
- Published in:
- 2013
- By:
- Publication type:
- Letter
Delayed warfarin induced skin necrosis in a patient with poor warfarin metabolizing activity due to interrupted warfarin therapy.
- Published in:
- 2013
- By:
- Publication type:
- Letter
APTT Reagents for Different Coagulation Tests: One Size Does Not Fit All.
- Published in:
- American Journal of Clinical Pathology, 2012, v. 138, n. 5, p. 757, doi. 10.1309/AJCPDHOK9TPPLUFN
- By:
- Publication type:
- Article
Non conventional mutations associated with myeloproliferative disorders are absent in splanchnic venous thrombosis cases.
- Published in:
- Liver International, 2012, v. 32, n. 10, p. 1596, doi. 10.1111/j.1478-3231.2012.02851.x
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- Publication type:
- Article
Hereditary protein C deficiency in Indian patients with venous thrombosis.
- Published in:
- Annals of Hematology, 2012, v. 91, n. 9, p. 1471, doi. 10.1007/s00277-012-1483-5
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- Publication type:
- Article
Bone health in persons with haemophilia: a review.
- Published in:
- European Journal of Haematology, 2012, v. 89, n. 2, p. 95, doi. 10.1111/j.1600-0609.2012.01803.x
- By:
- Publication type:
- Article
A novel ELISA for diagnosis of Glanzmann's thrombasthenia and the heterozygote carriers.
- Published in:
- Annals of Hematology, 2012, v. 91, n. 6, p. 917, doi. 10.1007/s00277-011-1390-1
- By:
- Publication type:
- Article
Hemostasis Research in India: Past, Present, and Future.
- Published in:
- Clinical & Applied Thrombosis/Hemostasis, 2012, v. 18, n. 2, p. 128, doi. 10.1177/1076029611418965
- By:
- Publication type:
- Article
Pathophysiology of acquired von Willebrand disease: a concise review.
- Published in:
- European Journal of Haematology, 2011, v. 87, n. 2, p. 99, doi. 10.1111/j.1600-0609.2011.01636.x
- By:
- Publication type:
- Article
Challenges of multiple mutations in individual patients with haemophilia.
- Published in:
- European Journal of Haematology, 2011, v. 86, n. 3, p. 185, doi. 10.1111/j.1600-0609.2010.01564.x
- By:
- Publication type:
- Article
Differences in Etiological and Clinical Manifestations in Upper Extremity and Lower Limb Deep Venous Thrombosis Patients From India.
- Published in:
- Clinical & Applied Thrombosis/Hemostasis, 2010, v. 16, n. 6, p. 698, doi. 10.1177/1076029609351290
- By:
- Publication type:
- Article
Protein C ( PROC) gene mutations in two Indian families with purpura fulminans.
- Published in:
- 2010
- By:
- Publication type:
- Letter