Thrombotic microangiopathy
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00179906%3A_____%2F11%3A10105367" target="_blank" >RIV/00179906:_____/11:10105367 - isvavai.cz</a>
Alternative codes found
RIV/00216208:11150/11:10105367
Result on the web
<a href="http://www.sciencedirect.com/science/article/pii/S1473050211001194" target="_blank" >http://www.sciencedirect.com/science/article/pii/S1473050211001194</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1016/j.transci.2011.07.002" target="_blank" >10.1016/j.transci.2011.07.002</a>
Alternative languages
Result language
angličtina
Original language name
Thrombotic microangiopathy
Original language description
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. Thisarticle 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.
Czech name
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Czech description
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Classification
Type
J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)
CEP classification
FD - Oncology and haematology
OECD FORD branch
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Result continuities
Project
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Continuities
V - Vyzkumna aktivita podporovana z jinych verejnych zdroju
Others
Publication year
2011
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Transfusion and Apheresis Science
ISSN
1473-0502
e-ISSN
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Volume of the periodical
45
Issue of the periodical within the volume
2
Country of publishing house
GB - UNITED KINGDOM
Number of pages
5
Pages from-to
119-123
UT code for WoS article
000296406200003
EID of the result in the Scopus database
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