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TTP-like syndrome: novel concept and molecular pathogenesis of endotheliopathy-associated vascular microthrombotic disease

TTP is characterized by microangiopathic hemolytic anemia and thrombocytopenia associated with brain and kidney dysfunction. It occurs due to ADAMTS13 deficiency. TTP-like syndrome occurs in critically ill patients with the similar hematologic changes and additional organ dysfunction syndromes. Vasc...

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Dades bibliogràfiques
Publicat a:Thromb J
Autor principal: Chang, Jae C.
Format: Artigo
Idioma:Inglês
Publicat: BioMed Central 2018
Matèries:
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC6087012/
https://ncbi.nlm.nih.gov/pubmed/30127669
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12959-018-0174-4
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