31 results on '"Chamouni, Pierre"'
Search Results
2. Obstetrical complications in hereditary fibrinogen disorders: the Fibrinogest study
3. Management of patients with inherited bleeding disorders in oral surgery: A 13-year experience
4. Factor XII deficiency evaluated by thrombin generation assay
5. Evaluation of thrombin generation assay in factor XI deficiency
6. Management of von Willebrand disease with a factor VIII‐poor von Willebrand factor concentrate: Results from a prospective observational post‐marketing study
7. P1672: OCCUPATIONAL INTEGRATION OF ADULTS WITH SEVERE HAEMOPHILIA (INTHEMO): A STUDY BASED ON THE FRANCECOAG REGISTRY
8. Heterozygous large deletion mimicking homozygous substitution in MCFD2 in a patient with combined Factor V and Factor VIII deficiency.
9. A French Real-World Evidence Study Evaluating the Efficacy, Safety, and Pharmacokinetic Parameters of rVIII-SingleChain in Patients with Hemophilia A Receiving Prophylaxis
10. 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.
11. Modèle hub & spoke en France : organisation des soins et parcours des patients pour la thérapie génique de l'hémophilie.
12. Effectiveness of long‐term prophylaxis using pdFVIII / VWF concentrate in patients with inherited von Willebrand disease
13. Revised terminal half‐life of nonacog alfa as derived from extended sampling data: A real‐world study involving 64 haemophilia B patients on nonacog alfa regular prophylaxis
14. Prostate biopsy and prostate cancer management in patients with haemophilia: The experience of French Haemophilia Treatment Centres
15. First observation of inhibitor development against efmoroctocog alfa in France
16. Gastrointestinal bleeding from angiodysplasia in von Willebrand disease: Improved diagnosis and outcome prediction using videocapsule on top of conventional endoscopy
17. Afibrinogenemia with two compound heterozygous mutations in FGA gene
18. The Hemarthrosis-Simulating Knee Model: A Useful Tool for Individualized Education in Patients with Hemophilia (GEFACET Study)
19. Effectiveness of long‐term prophylaxis using pdFVIII/VWF concentrate in patients with inherited von Willebrand disease.
20. The Hemarthrosis-Simulating Knee Model: A Useful Tool for Individualized Education in Patients with Hemophilia (GEFACET Study)
21. Management of von Willebrand disease with a factor VIII‐poor von Willebrand factor concentrate: Results from a prospective observational post‐marketing study
22. Abnormal bleeding phenotype for mild haemophilia B patients with the p.Ile112Thr variation on the gene for factor IX
23. 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?
24. Assessment of prolonged hospital stay attributable to surgical site infections using appropriateness evaluation protocol
25. Abnormal bleeding phenotype for mild haemophilia B patients with the p.Ile112Thr variation on the gene for factor IX.
26. The Hemarthrosis-Simulating Knee Model: A Useful Tool for Individualized Education in Patients with Hemophilia (GEFACET Study).
27. Variants du facteur VII de la coagulation : quelle thromboplastine utiliser pour doser son activité ?
28. Congenital factor XIII deficiency: comprehensive overview of the FranceCoag cohort.
29. Determinants of adherence and consequences of the transition from adolescence to adulthood among young people with severe haemophilia (TRANSHEMO): study protocol for a multicentric French national observational cross-sectional study
30. Factor VII variants: which thromboplastin is the most relevant for FVII activity measurement?
31. Management of congenital quantitative fibrinogen disorders: a Delphi consensus.
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