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Real Life Population Pharmacokinetics Modelling of Eight Factors VIII in Patients with Severe Haemophilia A: Is It Always Relevant to Switch to an Extended Half-Life?
- Published in:
- Pharmaceutics, 2020, v. 12, n. 4, p. 380, doi. 10.3390/pharmaceutics12040380
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- 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
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- Article
Gestion d'un placenta percreta chez une patiente atteinte d'une hypofibrinogénémie congénitale sévère.
- Published in:
- Annales de Biologie Clinique, 2023, v. 81, n. 2, p. 210, doi. 10.1684/abc.2023.1802
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- Publication type:
- Article
Switch vers un facteur VIII recombinant fusionné avec un fragment Fc Expérience chez 30 patients hémophiles A.
- Published in:
- Annales de Biologie Clinique, 2020, v. 78, n. 1, p. 35, doi. 10.1684/abc.2020.1520
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- Article
Congenital factor XIII deficiency: comprehensive overview of the FranceCoag cohort.
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- British Journal of Haematology, 2020, v. 188, n. 2, p. 317, doi. 10.1111/bjh.16133
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- 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
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- Article
Emergency management of patients with Glanzmann thrombasthenia: consensus recommendations from the French reference center for inherited platelet disorders.
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- Orphanet Journal of Rare Diseases, 2023, v. 18, n. 1, p. 1, doi. 10.1186/s13023-023-02787-2
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- Publication type:
- Article
Efficacy, tolerability, and safety of an innovative medical device for improving oral accessibility during oral examination in special-needs patients: A multicentric clinical trial.
- Published in:
- PLoS ONE, 2020, v. 15, n. 9, p. 1, doi. 10.1371/journal.pone.0239898
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- Article
Efficacy of octreotide in the treatment of gastrointestinal angiodysplasia in a patient with Glanzmann thrombasthenia.
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- Transfusion Medicine, 2022, v. 32, n. 6, p. 519, doi. 10.1111/tme.12911
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- Article
Use of recombinant Von Willebrand factor during transcatheter aortic valve replacement in a patient with acquired von Willebrand syndrome.
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- Transfusion Medicine, 2021, v. 31, n. 2, p. 142, doi. 10.1111/tme.12765
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- Article
COVID-19 in a pediatric patient with Glanzmann thrombasthenia.
- Published in:
- 2020
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- Publication type:
- Letter
Determinants of adherence and consequences of the transition from adolescence to adulthood among young people with severe haemophilia (TRANSHEMO): A multicentric French national observational cross‐sectional study based on the FranceCoag registry.
- Published in:
- Haemophilia, 2023, v. 29, n. 5, p. 1202, doi. 10.1111/hae.14841
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- Publication type:
- Article
Efficacy and safety of a recombinant Von Willebrand Factor treatment in patients with inherited Von Willebrand Disease requiring surgical procedures.
- Published in:
- Haemophilia, 2021, v. 27, n. 2, p. 270, doi. 10.1111/hae.14242
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- Publication type:
- Article