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11. [Diagnosis of inherited diseases of platelet function. Interdisciplinary S2K guideline of the Permanent Paediatric Committee of the Society of Thrombosis and Haemostasis Research (GTH e. V.)]. Knöfler R, Eberl W, Schulze H, Bakchoul T, Bergmann F, Gehrisch S, Geisen C, Gottstein S, Halimeh S, Harbrecht U, Kappert G, Kirchmaier C, Kehrel B, Lösche W, Krause M, Mahnel R, Meyer O, Pilgrimm AK, Pillitteri D, Rott H, Santoso S, Siegemund A, Schambeck C, Scheer M, Schmugge M, Scholl T, Strauss G, Zieger B, Zotz R, Hermann M, Streif W. Hamostaseologie; 2014 Feb; 34(3):201-12. PubMed ID: 24903476 [Abstract] [Full Text] [Related]
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18. Testing for inherited platelet defects in clinical laboratories in Germany, Austria and Switzerland. Results of a survey carried out by the Permanent Paediatric Group of the German Thrombosis and Haemostasis Research Society (GTH). Streif W, Oliveri M, Weickardt S, Eberl W, Knoefler R, Thromkid Study Group of GTH. Platelets; 2010 Dec; 21(6):470-8. PubMed ID: 20635849 [Abstract] [Full Text] [Related]
20. The level of laboratory testing required for diagnosis or exclusion of a platelet function disorder using platelet aggregation and secretion assays. Mezzano D, Quiroga T, Pereira J. Semin Thromb Hemost; 2009 Mar; 35(2):242-54. PubMed ID: 19408197 [Abstract] [Full Text] [Related] Page: [Next] [New Search]