Factor XI replacement for inherited factor XI deficiency in routine clinical practice: results of the HEMOLEVEN prospective 3‐year postmarketing study-Reference-Cited by-同舟云学术

Factor XI replacement for inherited factor XI deficiency in routine clinical practice: results of the HEMOLEVEN prospective 3‐year postmarketing study

Published:2015-03-26 Issue:4 Volume:21 Page:481-489
ISSN:1351-8216
Container-title:Haemophilia
language:en
Short-container-title:Haemophilia

Author:

Bauduer F.¹,Raucourt E.²,Boyer‐Neumann C.³,Trossaert M.⁴,Beurrier P.⁵,Faradji A.⁶,Peynet J.²,Borg J.‐Y.⁷,Chamouni P.⁷,Chatelanaz C.⁸,Henriet C.⁸,Bridey F.⁸,Goudemand J.⁹,

Affiliation:

1. Clinical Haematology Centre Hospitalier de la Côte Basque, Bayonne and Laboratory MRGM University of Bordeaux Bordeaux France

2. Haemophilia Treatment Center CH Le Chesnay Le Chesnay France

3. Haematology Department CHU Antoine Beclère Clamart France

4. Haematology Department CHU Nantes Nantes France

5. Haemophilia Treatment Center CHU Angers Angers France

6. Haemophilia Treatment Center Haematology Department Hautepierre Hospital Strasbourg France

7. Haemostasis Unit‐CRTH CHRU Hôpital Charles Nicolle Rouen France

8. Laboratoire français du Fractionnement et des Biotechnologies (LFB) Les Ulis France

9. Hematology and Transfusion Faculté de Médecine Lille University Hospital Lille 2 University Lille France

Publisher

Wiley

Subject

Genetics(clinical),Hematology,General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/hae.12655

Reference29 articles.

1. 10 Factor XI deficiency

2. www.wfh.orgAnnual global survey 2013

3. Factor XI Deficiency in Ashkenazi Jews in Israel

4. Factor XI deficiency—resolving the enigma?

5. Congenital Factor XI Deficiency: An Update

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