Inherited Giant Platelet Disorders
Author:
Affiliation:
1. Departments of Pathology at Baylor College of Medicine and The Methodist Hospital, Houston, TX.
Publisher
Oxford University Press (OUP)
Subject
General Medicine
Link
http://academic.oup.com/ajcp/article-pdf/113/2/176/24980480/ajcpath113-0176.pdf
Reference92 articles.
1. Kehrel B, Kronenberg A, Schwippert B, et al. Thrombospondin binds normally to glycoprotein IIIb deficient platelets. Biochem Biophys Res Comm. 1991;179:985-991.
2. Asch AS, Barnwell J, Silverstein RL, et al. Isolation of the thrombospondin membrane receptor. J Clin Invest. 1987;79:1054-1061.
3. Takashima T, Maeda H, Koyanagi T, et al. Prenatal diagnosis and obstetrical management of May-Hegglin anomaly: a case report. Fetal Diagn Ther. 1992;7:186-189.
4. Hamilton WR, Shaikh BS, Ottie JN, et al. Platelet function, ultrastructure and survival in the May-Hegglin anomaly. Am J Clin Pathol. 1980;74:663-668.
5. Noris P, Spedini P, Belletti S, et al. Thrombocytopenia, giant platelets and leukocyte inclusion bodies (MHA): clinical and laboratory findings. Am J Med. 1998;194:355-360.
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