| Thrombotic microangiopathy. | |
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MedLine Citation:
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PMID: 21885345 Owner: NLM Status: Publisher |
Abstract/OtherAbstract:
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Thrombotic microangiopathy (TMA) is a histopathological feature of various diseases including thrombotic thrombocytopenic purpura (TTP) and hemolytic uremic syndrome (HUS). There are many secondary causes of TMA, many of them could mimic TTP or HUS. This article presents a short overview on TMA. In conclusion TMA is the result of various etiology reasons and pathologic reactions with various clinical entities. It is important to focus on a thorough history including family history when deciding on a diagnosis. Analysis of ADAMTS 13 and ADAMTS 13-antibodies may help to decide continued therapy. |
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Authors:
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M Mörtzell; G Berlin; T Nilsson; C G Axelsson; M Efvergren; J Audzijoni; A Griskevicius; J Ptak; M Blaha; H Tomsova; G M Limbruno; P Centoni; E Newman; S Eloot; A Dhondt; J Tomaz; V Witt; G Rock; B Stegmayr |
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Publication Detail:
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Type: JOURNAL ARTICLE Date: 2011-8-30 |
Journal Detail:
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Title: Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis Volume: - ISSN: 1473-0502 ISO Abbreviation: - Publication Date: 2011 Aug |
Date Detail:
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Created Date: 2011-9-2 Completed Date: - Revised Date: - |
Medline Journal Info:
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Nlm Unique ID: 101095653 Medline TA: Transfus Apher Sci Country: - |
Other Details:
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Languages: ENG Pagination: - Citation Subset: - |
Copyright Information:
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Copyright © 2011 Elsevier Ltd. All rights reserved. |
Affiliation:
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Department of Public Health and Medicine, Umeå University, Umea, Sweden. |
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From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine
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