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Res Pract Thromb Haemost. 2017 Aug 24;1(2):291-295. doi: 10.1002/rth2.12033. eCollection 2017 Oct.

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

Research and practice in thrombosis and haemostasis

David J Rabbolini, Elizabeth E Gardiner, Marie-Christine Morel-Kopp, Scott Dunkley, Anila Jahangiri, Christine S-M Lee, William S Stevenson, Christopher M Ward

Affiliations

  1. Department of Haematology and Transfusion Medicine Royal North Shore Hospital Sydney NSW Australia.
  2. Northern Blood Research Centre Kolling Institute of Medical Research University of Sydney Sydney NSW Australia.
  3. ACRF Department of Cancer Biology and Therapeutics John Curtin School of Medical Research Australian National University Canberra ACT Australia.
  4. The Royal Prince Alfred Hospital Sydney NSW Australia.

PMID: 30046699 PMCID: PMC6058269 DOI: 10.1002/rth2.12033

Abstract

Idiopathic immune thrombocytopenia (ITP) is an autoimmune disorder characterized by relapsing/ remitting thrombocytopenia. Bleeding complications are infrequent with platelet counts above 30×10

Keywords: collagen; immune; platelet membrane glycoproteins; purpura; thrombocytopenia

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