| A review of long-term prophylaxis in the rare inherited coagulation factor deficiencies. | |
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MedLine Citation:
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PMID: 19906159 Owner: NLM Status: MEDLINE |
Abstract/OtherAbstract:
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The rare inherited coagulation factor deficiencies (deficiencies of factors I, II, V, VII, XI, XIII, combined FV + FVII deficiency, combined deficiency of the vitamin K dependent factors and von Willebrand disease type 3) have an aggregate prevalence of approximately 1:100,000. They may cause recurrent life or function threatening haemorrhage. In this article we review the available literature on long-term prophylaxis and, where possible, make recommendations on this important area. |
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Authors:
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T Todd; D J Perry |
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Publication Detail:
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Type: Journal Article; Review Date: 2009-11-11 |
Journal Detail:
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Title: Haemophilia : the official journal of the World Federation of Hemophilia Volume: 16 ISSN: 1365-2516 ISO Abbreviation: Haemophilia Publication Date: 2010 Jul |
Date Detail:
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Created Date: 2010-07-20 Completed Date: 2011-01-05 Revised Date: - |
Medline Journal Info:
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Nlm Unique ID: 9442916 Medline TA: Haemophilia Country: England |
Other Details:
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Languages: eng Pagination: 569-83 Citation Subset: IM |
Affiliation:
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Department of Haematology, Royal Devon and Exeter Hospital, Exeter, UK. anthony.todd@rdeft.nhs.uk |
Export Citation:
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APA/MLA Format Download EndNote Download BibTex |
| MeSH Terms | |
Descriptor/Qualifier:
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Blood Coagulation Disorders
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drug therapy* Blood Coagulation Factors / administration & dosage, therapeutic use* Fibrinogen Humans Vitamin K Deficiency / drug therapy |
| Chemical | |
Reg. No./Substance:
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0/Blood Coagulation Factors; 9001-32-5/Fibrinogen |
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
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