Pharmacokinetics of recombinant factor XIII at steady state in patients with congenital factor XIII A-subunit deficiency-Reference-Cited by-同舟云学术

Pharmacokinetics of recombinant factor XIII at steady state in patients with congenital factor XIII A-subunit deficiency

Published:2014-10-25 Issue:12 Volume:12 Page:2038-2043
ISSN:1538-7933
Container-title:Journal of Thrombosis and Haemostasis
language:en
Short-container-title:J Thromb Haemost

Author:

Kerlin B.¹,Brand B.²,Inbal A.³,Halimeh S.⁴,Nugent D.⁵,Lundblad M.⁶,Tehranchi R.⁷

Affiliation:

1. Nationwide Children's Hospital and The Ohio State University College of Medicine; Columbus OH USA

2. University Hospital Zurich; Zurich Switzerland

3. Thrombosis and Hemostasis Unit; Hematology Department; Rabin Medical Center; Petah Tikva and Sackler Faculty of Medicine; Tel Aviv University; Tel Aviv Israel

4. Medical Thrombosis and Haemophilia Treatment Center; Duisburg Germany

5. Hematology; CHOC Children's Hospital/UC Irvine Medical School; Orange CA USA

6. Clinical Pharmacology Biopharm; Novo Nordisk A/S; Søborg Denmark

7. Medical and Science; Haemostasis R&D Portfolio; Novo Nordisk A/S; Søborg Denmark

Funder

Novo Nordisk A/S

Publisher

Wiley

Subject

Hematology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/jth.12739/fullpdf

Reference29 articles.

1. Factor XIII is a key molecule at the intersection of coagulation and fibrinolysis as well as inflammation and infection control;Ichinose;Int J Hematol,2012

2. Factor XIII deficiency;Karimi;Semin Thromb Hemost,2009

3. World Federation of Hemophilia Report on the Annual Global Survey 2011 http://www1.wfh.org/publications/files/pdf-1488.pdf

4. Prophylactic therapy with Fibrogammin P is associated with a decreased incidence of bleeding episodes: a retrospective study;Lusher;Haemophilia,2010

5. Pharmacokinetics and tolerability of factor XIII concentrates prepared from human placenta or plasma: a crossover randomised study;Brackmann;Thromb Haemost,1995

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