Found: 15
Select item for more details and to access through your institution.
Gingival bleeding is a useful clinical feature in the diagnosis of hereditary bleeding disorders in children.
- Published in:
- European Journal of Pediatrics, 2024, v. 183, n. 5, p. 2215, doi. 10.1007/s00431-024-05487-6
- By:
- Publication type:
- Article
Major surgery management in patients with haemophilia A and inhibitors on emicizumab prophylaxis without global coagulation monitoring.
- Published in:
- British Journal of Haematology, 2020, v. 189, n. 3, p. e100, doi. 10.1111/bjh.16512
- 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
Analysis of the genotypes and phenotypes of 37 unrelated patients with inherited factor VII deficiency.
- Published in:
- European Journal of Human Genetics, 2001, v. 9, n. 2, p. 105
- By:
- Publication type:
- Article
Argatroban in the management of heparin-induced thrombocytopenia: a multicenter clinical trial.
- Published in:
- 2015
- By:
- Publication type:
- journal article
Purpura fulminans due to imported falciparum malaria.
- Published in:
- 2008
- By:
- Publication type:
- Letter
Traitement antihémophilique et risque d'inhibiteurs chez l'hémophile A sévère : l'étude SIPPET démontre un avantage aux concentrés de facteur VIII d'origine plasmatique sur les concentrés recombinants.
- Published in:
- Hematologie, 2019, v. 25, n. 2, p. 93, doi. 10.1684/hma.2019.1461
- By:
- Publication type:
- Article
Secretion of functional plasma haemostasis proteins in long-term primary cultures of human hepatocytes.
- Published in:
- British Journal of Haematology, 2004, v. 125, n. 5, p. 638, doi. 10.1111/j.1365-2141.2004.04957.x
- By:
- Publication type:
- Article
Inherited factor VII deficiency and surgery: clinical data are the best criteria to predict the risk of bleeding.
- Published in:
- British Journal of Haematology, 2002, v. 117, n. 1, p. 172, doi. 10.1046/j.1365-2141.2002.03408.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
A focus on dominant negative variants in a series of 170 heterozygous FXI‐deficient patients.
- Published in:
- Haemophilia, 2023, v. 29, n. 4, p. 1113, doi. 10.1111/hae.14802
- By:
- Publication type:
- Article
Occupational integration of adults with severe haemophilia (INTHEMO): A study based on the FranceCoag registry.
- Published in:
- Haemophilia, 2022, v. 28, n. 6, p. 962, doi. 10.1111/hae.14620
- By:
- Publication type:
- Article
Prostate biopsy and prostate cancer management in patients with haemophilia: The experience of French Haemophilia Treatment Centres.
- Published in:
- Haemophilia, 2022, v. 28, n. 3, p. 437, doi. 10.1111/hae.14507
- By:
- Publication type:
- Article
The homozygous variant p.Gln1311* in exon 28 of VWF is associated with the development of alloantibodies in 3 unrelated patients with type 3 VWD.
- Published in:
- Haemophilia, 2021, v. 27, n. 4, p. e491, doi. 10.1111/hae.14207
- By:
- Publication type:
- Article