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Journal Abstract Search
265 related items for PubMed ID: 24903476
1. [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; 34(3):201-12. PubMed ID: 24903476 [Abstract] [Full Text] [Related]
4. 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; 21(6):470-8. PubMed ID: 20635849 [Abstract] [Full Text] [Related]
6. Genetic testing in the diagnostic evaluation of inherited platelet disorders. Nurden AT, Fiore M, Pillois X, Nurden P. Semin Thromb Hemost; 2009 Mar; 35(2):204-12. PubMed ID: 19408193 [Abstract] [Full Text] [Related]
7. ISTH bleeding assessment tool and platelet function analyzer in children with mild inherited platelet function disorders. Alhaj D, Hagedorn N, Cuntz F, Reschke M, Schuldes J, Ruthenberg J, Bakchoul T, Greinacher A, Holzhauer S. Eur J Haematol; 2024 Jul; 113(1):54-65. PubMed ID: 38549165 [Abstract] [Full Text] [Related]
8. PFA-100 system: a new method for assessment of platelet dysfunction. Mammen EF, Comp PC, Gosselin R, Greenberg C, Hoots WK, Kessler CM, Larkin EC, Liles D, Nugent DJ. Semin Thromb Hemost; 1998 Jul; 24(2):195-202. PubMed ID: 9579642 [Abstract] [Full Text] [Related]
9. 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]
10. Genetics of inherited platelet disorders. Gothwal M, Sandrock-Lang K, Zieger B. Hamostaseologie; 2014 Mar; 34(2):133-41. PubMed ID: 24352347 [Abstract] [Full Text] [Related]
11. Diagnostic assessment of platelet disorders: what are the challenges to standardization? Pai M, Hayward CP. Semin Thromb Hemost; 2009 Mar; 35(2):131-8. PubMed ID: 19408186 [Abstract] [Full Text] [Related]
14. Platelet function testing: auditing local practice and broader implications. Favaloro EJ, Mohammed S. Clin Lab Sci; 2010 Mar; 23(1):21-31. PubMed ID: 20218091 [Abstract] [Full Text] [Related]
16. Guidelines for the laboratory investigation of heritable disorders of platelet function. Harrison P, Mackie I, Mumford A, Briggs C, Liesner R, Winter M, Machin S, British Committee for Standards in Haematology. Br J Haematol; 2011 Oct; 155(1):30-44. PubMed ID: 21790527 [Abstract] [Full Text] [Related]
18. Platelet function defects. Simon D, Kunicki T, Nugent D. Haemophilia; 2008 Nov; 14(6):1240-9. PubMed ID: 19141164 [Abstract] [Full Text] [Related]
19. [First results of the THROMKID study: a quality project for the registration of children und adolescents with hereditary platelet function defects in Germany, Austria, and Switzerland]. Knöfler R, Olivieri M, Weickardt S, Eberl W, Streif W, THROMKID Studiengruppe der Gesellschaft für Thrombose- und Hämostaseforschung e.V. Hamostaseologie; 2007 Feb; 27(1):48-53. PubMed ID: 17279276 [Abstract] [Full Text] [Related]