Anti‐glycoprotein VI mediated immune thrombocytopenia: An under‐recognized and significant entity?

ESSENTIALS: Platelet function defects may cause atypical bleeding symptoms in immune thrombocytopenia (ITP). An isolated platelet defect of collagen‐induced aggregation was explored in a patient with ITP. ITP mediated by antibodies to glycoprotein (GP) VI curtail receptor function. Inclusion of GPVI...

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Detaylı Bibliyografya
Yayımlandı:Res Pract Thromb Haemost
Asıl Yazarlar: Rabbolini, David J., Gardiner, Elizabeth E., Morel‐Kopp, Marie‐Christine, Dunkley, Scott, Jahangiri, Anila, Lee, Christine S‐M., Stevenson, William S., Ward, Christopher M.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: John Wiley and Sons Inc. 2017
Konular:
Case Reports
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC6058269/
https://ncbi.nlm.nih.gov/pubmed/30046699
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/rth2.12033
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