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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
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
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
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
Blood coagulation in falciparum malariaâa review.
- Published in:
- Parasitology Research, 2008, v. 102, n. 4, p. 571, doi. 10.1007/s00436-007-0832-0
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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
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
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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
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
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
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
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
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
- By:
- Publication type:
- 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
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- Publication type:
- Article
Plasminogen activator inhibitor-1 4G/5G gene polymorphism in women with fetal loss
- Published in:
- 2009
- By:
- Publication type:
- journal article
Decrease in circulating percentage platelet microparticles during pregnancy-a different perspective.
- Published in:
- 2016
- 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
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
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
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
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
- 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
Deep venous thrombosis in the antenatal period in a large cohort of pregnancies from western India.
- Published in:
- Thrombosis Journal, 2007, v. 5, p. 9, doi. 10.1186/1477-9560-5-9
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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
- By:
- Publication type:
- Article
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
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- Publication type:
- Article
JAK2 Mutations Across a Spectrum of Venous Thrombosis Cases.
- Published in:
- American Journal of Clinical Pathology, 2010, v. 134, n. 1, p. 82, doi. 10.1309/AJCP7VO4HAIZYATP
- By:
- Publication type:
- Article
Reduced Clinical Severity in a Mutationally Well-Characterized Cohort of Severe Hemophilia With Associated Thrombophilia.
- Published in:
- American Journal of Clinical Pathology, 2008, v. 130, n. 1, p. 84, doi. 10.1309/6A8UURH9NU2YNFBP
- By:
- Publication type:
- Article
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
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
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- 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
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- 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
Amelioration of clinical severity of similar mutations severe factor IX deficiency by coinherited thrombophilia.
- Published in:
- 2008
- By:
- Publication type:
- Letter
Direct detection of factor IX gene deletions in Indian haemophiliacs by multiplex PCR.
- Published in:
- European Journal of Haematology, 2003, v. 71, n. 3, p. 233, doi. 10.1034/j.1600-0609.2003.00119.x
- By:
- Publication type:
- Article
Requiem to prenatal diagnosis of haemophilia A and B using coagulation activity and antigen based assays: not yet!
- Published in:
- European Journal of Haematology, 2003, v. 70, n. 4, p. 253, doi. 10.1034/j.1600-0609.2003.00056.x
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- Publication type:
- Article
Inherited deficiency of multiple vitamin K-dependent coagulation factors and coagulation inhibitors presenting as hemorrhagic diathesis, mental retardation, and growth retardation.
- Published in:
- American Journal of Hematology, 1996, v. 52, n. 1, p. 67, doi. 10.1002/(SICI)1096-8652(199605)52:1<67::AID-AJH18>3.0.CO;2-4
- By:
- Publication type:
- Article
Imaging the interaction between dengue 2 virus and human blood platelets using atomic force and electron microscopy.
- Published in:
- Journal of Electron Microscopy, 2008, v. 57, n. 3, p. 113, doi. 10.1093/jmicro/dfn007
- By:
- Publication type:
- Article
Protein C ( PROC) gene mutations in two Indian families with purpura fulminans.
- Published in:
- 2010
- By:
- Publication type:
- Letter
A common G10430A mutation (Gly 60 Ser) in the factor IX gene describes the presence of moderate and mild hemophilia B in the majority of the Gujarati population.
- Published in:
- Annals of Hematology, 2007, v. 86, n. 5, p. 377, doi. 10.1007/s00277-007-0250-5
- By:
- Publication type:
- Article
The spectrum of bleeding disorders in women with menorrhagia: a report from Western India.
- Published in:
- Annals of Hematology, 2005, v. 84, n. 5, p. 339, doi. 10.1007/s00277-004-0905-4
- By:
- Publication type:
- Article
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
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
- By:
- Publication type:
- Case Study
Mutations in the MCFD2 gene and a novel mutation in the LMAN1 gene in Indian families with combined deficiency of factor V and VIII.
- Published in:
- American Journal of Hematology, 2005, v. 79, n. 4, p. 262, doi. 10.1002/ajh.20397
- By:
- Publication type:
- Article
Major disorganization of factor VIII gene as a cause of severe hemophilia A in Indian patients.
- Published in:
- American Journal of Hematology, 2004, v. 76, n. 1, p. 96, doi. 10.1002/ajh.20031
- By:
- Publication type:
- Article
Factor VIII and IX gene polymorphisms and carrier analysis in Indian population.
- Published in:
- American Journal of Hematology, 1997, v. 54, n. 4, p. 271, doi. 10.1002/(SICI)1096-8652(199704)54:4<271::AID-AJH2>3.0.CO;2-S
- By:
- Publication type:
- Article
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
- By:
- Publication type:
- Article
Double mutations causing haemophilia B: a double whammy!
- Published in:
- 2009
- By:
- Publication type:
- Letter