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827 related items for PubMed ID: 20941465
1. Prospective study of low-dose ristocetin-induced platelet aggregation to identify type 2B von Willebrand disease (VWD) and platelet-type VWD in children. Frontroth JP, Hepner M, Sciuccati G, Feliú Torres A, Pieroni G, Bonduel M. Thromb Haemost; 2010 Dec; 104(6):1158-65. PubMed ID: 20941465 [Abstract] [Full Text] [Related]
2. A first Taiwanese Chinese family of type 2B von Willebrand disease with R1306W mutation. Shen MC, Lin JS, Lin DS, Hsu SC, Lin B. Thromb Res; 2003 Dec; 112(5-6):291-5. PubMed ID: 15041272 [Abstract] [Full Text] [Related]
6. Measurement of von Willebrand factor binding to a recombinant fragment of glycoprotein Ibalpha in an enzyme-linked immunosorbent assay-based method: performances in patients with type 2B von Willebrand disease. Caron C, Hilbert L, Vanhoorelbeke K, Deckmyn H, Goudemand J, Mazurier C. Br J Haematol; 2006 Jun; 133(6):655-63. PubMed ID: 16704443 [Abstract] [Full Text] [Related]
9. von Willebrand disease in a pediatric-based population--comparison of type 1 diagnostic criteria and use of the PFA-100 and a von Willebrand factor/collagen-binding assay. Dean JA, Blanchette VS, Carcao MD, Stain AM, Sparling CR, Siekmann J, Turecek PL, Lillicrap D, Rand ML. Thromb Haemost; 2000 Sep; 84(3):401-9. PubMed ID: 11019962 [Abstract] [Full Text] [Related]
11. Evaluation of an heterogeneous group of patients with von Willebrand disease using an assay alternative to ristocetin induced platelet agglutination. Stufano F, Baronciani L, Pagliari MT, Franchi F, Cozzi G, Garcia-Oya I, Bucciarelli P, Boscarino M, Peyvandi F. J Thromb Haemost; 2015 Oct; 13(10):1806-14. PubMed ID: 26206100 [Abstract] [Full Text] [Related]
12. Response of von Willebrand factor parameters to desmopressin in patients with type 1 and type 2 congenital von Willebrand disease: diagnostic and therapeutic implications. Michiels JJ, van de Velde A, van Vliet HH, van der Planken M, Schroyens W, Berneman Z. Semin Thromb Hemost; 2002 Apr; 28(2):111-32. PubMed ID: 11992235 [Abstract] [Full Text] [Related]
13. Identification of p.W246L as a novel mutation in the GP1BA gene responsible for platelet-type von Willebrand disease. Woods AI, Sanchez-Luceros A, Bermejo E, Paiva J, Alberto MF, Grosso SH, Kempfer AC, Lazzari MA. Semin Thromb Hemost; 2014 Mar; 40(2):151-60. PubMed ID: 24474090 [Abstract] [Full Text] [Related]