This five-volume series provides clinicians with a detailed, up-to-date, well-referenced overview of the latest developments in this rapidly expanding feld. It serves as an
authoritative guide to the diagnosis and treatment of platelet disorders.The primary audience for the series is clinicians, residents and fellows in internal medicine,
cardiology and haematology, as well as clinicians (e.g. neurologists, nephrologists, rheumatologists) and basic scientists who may be concerned with disorders and
cellular mechanisms involving platelets.
Chapter 60: Approach to patients with suspected platelet-related bleeding.- Chapter 61: Inherited thrombocytopenias.- Chapter 62: Immune thrombocytopenia.- Chapter 63: Fetal and neonatal alloimmune thrombocytopenia.- Chapter 64: Drug-induced thrombocytopenia.- Chapter 65: Thrombocytopenia in pregnancy.- Chapter 66: Thrombocytopenia in cancer.- Chapter 67: Miscellaneous causes of thrombocytopenia.- Chapter 68: Inherited platelet function disorders: adhesive protein defects.- Chapter 69: Inherited platelet function disorders: G protein-coupled receptor defects.- Chapter 70: Inherited platelet function disorders: defects of content and secretion of platelet granules.- Chapter 71: Inherited platelet function disorders: signal transduction defects.- Chapter 72: Inherited platelet disorders: defects of transcription factors.- Chapter 73: Inherited platelet function disorders: defects of cytoskeletal proteins.- Chapter 74: Inherited platelet function disorders: defects of membrane phospholipids.- Chapter 75: Inherited platelet function disorders: Quebec platelet disorder.- Chapter 76: Acquired disorders of platelet function.- Chapter 77: Management of bleeding in antiplatelet-treated patients.- Chapter 78: Autoimmune platelet function disorders.
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