Found: 16
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Progressive endothelial damage revealed by multilevel von Willebrand factor plasma concentrations in atrial fibrillation patients.
- Published in:
- 2013
- By:
- Publication type:
- Journal Article
Progressive endothelial damage revealed by multilevel von Willebrand factor plasma concentrations in atrial fibrillation patients.
- Published in:
- EP: Europace, 2013, v. 15, n. 11, p. 1562, doi. 10.1093/europace/eut121
- By:
- Publication type:
- Article
Effectiveness and safety of hFVIII/VWF concentrate (Voncento®) in patients with inherited von Willebrand disease requiring surgical procedures: the OPALE multicentre observational study.
- Published in:
- Blood Transfusion (17232007), 2021, v. 19, n. 2, p. 152, doi. 10.2450/2020.0246-20
- By:
- Publication type:
- Article
Acquired factor V inhibitor: a nation‐wide study of 38 patients.
- Published in:
- British Journal of Haematology, 2021, v. 192, n. 5, p. 892, doi. 10.1111/bjh.17308
- By:
- Publication type:
- Article
Congenital factor XIII deficiency: comprehensive overview of the FranceCoag cohort.
- Published in:
- British Journal of Haematology, 2020, v. 188, n. 2, p. 317, doi. 10.1111/bjh.16133
- By:
- Publication type:
- Article
Management of rare inherited bleeding disorders: Proposals of the French Reference Centre on Haemophilia and Rare Coagulation Disorders.
- Published in:
- European Journal of Haematology, 2023, v. 110, n. 6, p. 584, doi. 10.1111/ejh.13941
- By:
- Publication type:
- Article
Effectiveness of long‐term prophylaxis using pdFVIII/VWF concentrate in patients with inherited von Willebrand disease.
- Published in:
- European Journal of Haematology, 2022, v. 109, n. 1, p. 109, doi. 10.1111/ejh.13778
- By:
- Publication type:
- Article
Déficit congénital en facteur XIII en 2020 Prévalence, diagnostic clinique et biologique et modalités thérapeutiques.
- Published in:
- Hematologie, 2020, v. 26, n. 4, p. 192, doi. 10.1684/hma.2020.1571
- By:
- Publication type:
- Article
A risk score for the management of pregnant women with increased risk of venous thromboembolism: a multicentre prospective study.
- Published in:
- British Journal of Haematology, 2009, v. 145, n. 6, p. 825, doi. 10.1111/j.1365-2141.2009.07698.x
- By:
- Publication type:
- Article
Erratum: Molecular bases of antithrombin deficiency: twenty-two novel mutations in the antithrombin gene.
- Published in:
- Human Mutation, 2006, v. 27, n. 11, p. 1160, doi. 10.1002/humu.9468
- By:
- Publication type:
- Article
Molecular bases of antithrombin deficiency: twenty-two novel mutations in the antithrombin gene.
- Published in:
- Human Mutation, 2006, v. 27, n. 6, p. 600, doi. 10.1002/humu.9425
- By:
- Publication type:
- Article
Report of surgeries, their outcome and the thrombin generation assay in patients with Factor XI deficiency: A retrospective single‐centre study.
- Published in:
- Haemophilia, 2022, v. 28, n. 2, p. 301, doi. 10.1111/hae.14506
- By:
- Publication type:
- Article
Management of previously untreated patients with severe haemophilia A preferentially treated with recombinant factor VIII products: Two French centres' real‐life experience.
- Published in:
- Haemophilia, 2020, v. 26, n. 6, p. e349, doi. 10.1111/hae.14132
- By:
- Publication type:
- Article
Benefits of thromboelastometry for monitoring replacement therapy in patients with severe inherited factor XIII deficiency: 3 illustrative cases.
- Published in:
- Haemophilia, 2019, v. 25, n. 5, p. e336, doi. 10.1111/hae.13823
- By:
- Publication type:
- Article
A single‐centre study of management of pregnant women with von Willebrand disease.
- Published in:
- 2019
- By:
- Publication type:
- Letter to the Editor
Relationships between severe neonatal thrombocytopenia and maternal characteristics in pregnancies associated with autoimmune thrombocytopenia.
- Published in:
- British Journal of Haematology, 1998, v. 103, n. 2, p. 397, doi. 10.1046/j.1365-2141.1998.01006.x
- By:
- Publication type:
- Article