| Atypical hemolytic uremic syndrome associated with mutations in complement regulator genes. | |
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MedLine Citation:
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PMID: 20865641 Owner: NLM Status: In-Process |
Abstract/OtherAbstract:
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In the last 10 years the knowledge of the pathophysiology of atypical hemolytic uremic syndrome (aHUS) has substantially increased. Nevertheless, aHUS remains a severe disorder, in which early recognition of symptoms remains a key issue. The landmark discovery of genetic abnormalities in complement regulatory genes in most patients gave us new insights into the influence of each abnormality on the disease outcome and opened new perspectives for patient management. This allows a potentially more tailored approach in treating aHUS patients. |
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Authors:
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Moglie Le Quintrec; Lubka Roumenina; Marina Noris; Véronique Frémeaux-Bacchi |
Publication Detail:
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Type: Journal Article; Research Support, Non-U.S. Gov't Date: 2010-09-23 |
Journal Detail:
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Title: Seminars in thrombosis and hemostasis Volume: 36 ISSN: 1098-9064 ISO Abbreviation: Semin. Thromb. Hemost. Publication Date: 2010 Sep |
Date Detail:
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Created Date: 2010-09-24 Completed Date: - Revised Date: - |
Medline Journal Info:
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Nlm Unique ID: 0431155 Medline TA: Semin Thromb Hemost Country: United States |
Other Details:
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Languages: eng Pagination: 641-52 Citation Subset: IM |
Copyright Information:
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© Thieme Medical Publishers. |
Affiliation:
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Service de Néphrologie, Hôpital Foch, 40 rue Worth, Suresnes, Paris, France. |
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From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
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