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dc.contributor.authorBesbas, N.
dc.contributor.authorKarpman, D.
dc.contributor.authorLandau, D.
dc.contributor.authorLoirat, C.
dc.contributor.authorProesmans, W.
dc.contributor.authorRemuzzi, G.
dc.contributor.authorRizzoni, G.
dc.contributor.authorTaylor, C. M.
dc.contributor.authorVan de Kar, N.
dc.contributor.authorZimmerhackl, L. B.
dc.date.accessioned2019-12-10T10:41:20Z
dc.date.available2019-12-10T10:41:20Z
dc.date.issued2006
dc.identifier.issn0085-2538
dc.identifier.urihttps://doi.org/10.1038/sj.ki.5001581
dc.identifier.urihttp://hdl.handle.net/11655/14175
dc.description.abstractThe diagnostic terms hemolytic uremic syndrome (HUS) and thrombotic thrombocytopenic purpura (TTP) are based on historical and overlapping clinical descriptions. Advances in understanding some of the causes of the syndrome now permit many patients to be classified according to etiology. The increased precision of a diagnosis based on causation is important for considering logical approaches to treatment and prognosis. It is also essential for research. We propose a classification that accommodates both a current understanding of causation (level 1) and clinical association in cases for whom cause of disease is unclear (level 2). We tested the classification in a pediatric disease registry of HUS. The revised classification is a stimulus to comprehensive investigation of all cases of HUS and TTP and is expected to increase the proportion of cases in whom a level 1 etiological diagnosis is confirmed.
dc.language.isoen
dc.publisherElsevier Science Inc
dc.relation.isversionof10.1038/sj.ki.5001581
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectUrology & Nephrology
dc.titleA Classification of Hemolytic Uremic Syndrome and Thrombotic Thrombocytopenic Purpura and Related Disorders
dc.typeinfo:eu-repo/semantics/review
dc.typeinfo:eu-repo/semantics/publishedVersion
dc.relation.journalKidney International
dc.contributor.departmentÇocuk Sağlığı ve Hastalıkları
dc.identifier.volume70
dc.identifier.issue3
dc.identifier.startpage423
dc.identifier.endpage431
dc.description.indexWoS


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