Works matching DE "BLOOD coagulation factor V"
Results: 29
Congenital factor V deficiency and decreased VWF in a Chinese male patient with hematuria.
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- Haemophilia, 2018, v. 24, n. 1, p. e16, doi. 10.1111/hae.13363
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- Article
Combined deficiency of factors V and VIII by chance coinheritance of parahaemophilia and haemophilia A, but not by mutations of either <italic>LMAN1</italic> or <italic>MCFD2,</italic> in a Japanese family.
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- Haemophilia, 2018, v. 24, n. 1, p. e13, doi. 10.1111/hae.13360
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- Article
Laparoscopic surgery in a woman with factor V deficiency: revisiting platelet factor V.
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- Haemophilia, 2016, v. 22, n. 4, p. e322, doi. 10.1111/hae.12946
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- Article
Characterization of an apparently synonymous F5 mutation causing aberrant splicing and factor V deficiency.
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- Haemophilia, 2015, v. 21, n. 2, p. 241, doi. 10.1111/hae.12554
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- Article
Asp68His mutation in the A1 domain of human factor V causes impaired secretion and ineffective translocation.
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- Haemophilia, 2014, v. 20, n. 4, p. e318, doi. 10.1111/hae.12476
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- Article
Acquired thrombin and FV inhibitors upon aortic bioprosthetic valve replacement.
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- Haemophilia, 2014, v. 20, n. 4, p. e354, doi. 10.1111/hae.12469
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- Article
Successful delivery in patients with severe congenital factor V deficiency: a study of five homozygous patients.
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- Haemophilia, 2013, v. 19, n. 5, p. e318, doi. 10.1111/hae.12210
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- Article
Severe factor V deficiency in two brothers with different clinical presentations.
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- Haemophilia, 2012, v. 18, n. 5, p. e383, doi. 10.1111/j.1365-2516.2012.02902.x
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- Article
Coinheritance of three novel FV gene mutations in a patient with a severe FV deficiency.
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- Haemophilia, 2012, v. 18, n. 2, p. e51, doi. 10.1111/j.1365-2516.2011.02747.x
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- Article
Functional characterization of a novel missense mutation identified in a Turkish patient affected by severe coagulation factor V deficiency.
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- Haemophilia, 2012, v. 18, n. 2, p. 205, doi. 10.1111/j.1365-2516.2011.02621.x
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- Article
Congenital Factor V Deficiency: Comparison of the Severity of Clinical Presentations among Patients with Rare Bleeding Disorders.
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- Acta Haematologica, 2015, v. 133, n. 2, p. 148, doi. 10.1159/000363598
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- Article
Modeling of human factor Va inactivation by activated protein C.
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- BMC Systems Biology, 2012, v. 6, n. 1, p. 45, doi. 10.1186/1752-0509-6-45
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- Article
Factor V Leiden and Inflammation.
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- Thrombosis, 2012, p. 1, doi. 10.1155/2012/594986
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- Article
Management of bleeding in severe factor V deficiency with a factor V inhibitor.
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- Vox Sanguinis, 2014, v. 107, n. 1, p. 97, doi. 10.1111/vox.12134
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- Article
Endocytosis of exogenous factor V by ex-vivo differentiated megakaryocytes from patients with severe parahaemophilia.
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- British Journal of Haematology, 2016, v. 175, n. 3, p. 517, doi. 10.1111/bjh.14262
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- Article
Coagulopathy triggered autoimmunity: experimental antiphospholipid syndrome in factor V Leiden mice.
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- BMC Medicine, 2013, v. 11, n. 1, p. 1, doi. 10.1186/1741-7015-11-92
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- Article
Multinuclear blue copper-proteins: the evolutionary design.
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- Journal of Evolutionary Biochemistry & Physiology, 2014, v. 50, n. 3, p. 189, doi. 10.1134/S0022093014030016
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- Article
Understanding Russell’s viper venom factor V activator’s substrate specificity by surface plasmon resonance and in-silico studies.
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- PLoS ONE, 2017, v. 12, n. 7, p. 1, doi. 10.1371/journal.pone.0181216
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- Article
Heritable thrombophilia testing in British Columbia: A report on practice patterns and prevalence.
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- British Columbia Medical Journal, 2013, v. 55, n. 3, p. 144
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- Article
A Hepatic Outflow Obstruction (Budd-Chiari Syndrome) Case Due to Multiple Hypercoagulable Status.
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- 2014
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- Case Study
Acquired factor V inhibitor in a patient with mantle cell lymphoma presenting with hematuria followed by thrombosis: a case report.
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- International Medical Case Reports Journal, 2014, v. 7, p. 27, doi. 10.2147/IMCRJ.S59236
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- Article
DockAFM: benchmarking protein structures by docking under AFM topographs.
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- Bioinformatics, 2013, v. 29, n. 24, p. 3230, doi. 10.1093/bioinformatics/btt561
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- Article
Hip Replacement Surgery in 14-Year-Old Girl with Factor V Deficiency: Haemostatic Treatment and Thromboprophylaxis.
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- Case Reports in Hematology, 2016, p. 1, doi. 10.1155/2016/5024692
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- Article
Factor V Arg506Gln Mutation Is Not Associated with Cardiovascular Mortality in Older Women.
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- American Journal of Epidemiology, 2009, v. 149, n. 7, p. 665
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- Article
A diagnostic algorithm for the detection of inhibitors against coagulation Factor V.
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- Clinical Chemistry & Laboratory Medicine, 2016, v. 54, n. 7, p. e203, doi. 10.1515/cclm-2015-1005
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- Article
The association of factor V Leiden with various clinical patterns of venous thromboembolism—the factor V Leiden paradox.
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- QJM: An International Journal of Medicine, 2014, v. 107, n. 9, p. 715, doi. 10.1093/qjmed/hcu055
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- Article
Single Nucleotide Polymorphisms Other than Factor V Leiden Are Associated with Coagulopathy and Osteonecrosis of the Femoral Head in Chinese Patients.
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- PLoS ONE, 2014, v. 9, n. 8, p. 1, doi. 10.1371/journal.pone.0104461
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- Article
Comparative Response of Platelet fV and Plasma fV to Activated Protein C and Relevance to a Model of Acute Traumatic Coagulopathy.
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- PLoS ONE, 2014, v. 9, n. 6, p. 1, doi. 10.1371/journal.pone.0099181
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- Article
Automated preparation of whole blood-derived platelets suspended in two different platelet additive solutions and stored for 7 days.
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- Transfusion, 2014, v. 54, n. 2, p. 426, doi. 10.1111/trf.12283
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- Article