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Thrombotic thrombocytopenic purpura possibly triggered by Graves’ disease
Thrombotic thrombocytopenic purpura (TTP) is a part of a spectrum of thrombotic microangiopathy syndromes which are mainly characterized by platelet aggregation causing microangiopathic hemolytic anemia, thrombocytopenia and microvascular occlusion. In literature, very few cases expressing a direct...
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| Yayımlandı: | Oxf Med Case Reports |
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| Asıl Yazarlar: | , , , , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Oxford University Press
2017
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5934682/ https://ncbi.nlm.nih.gov/pubmed/29744115 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/omcr/omx057 |
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