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209 related items for PubMed ID: 7741134
41. Characterization, classification, and treatment of von Willebrand diseases: a critical appraisal of the literature and personal experiences. Michiels JJ, Gadisseur A, Budde U, Berneman Z, van der Planken M, Schroyens W, van de Velde A, van Vliet H. Semin Thromb Hemost; 2005 Nov; 31(5):577-601. PubMed ID: 16276467 [Abstract] [Full Text] [Related]
42. In vivo experiments indicate that relatively high platelet deposition in von Willebrand's disease 'Vicenza' is caused by normal platelet-VWF levels rather than by high VWF-multimers in plasma. d'Alessio PA, Castaman G, Rodeghiero F, de Boer HC, Federici AB, Mannucci PM, de Groot PG, Sixma JJ, Zwaginga JJ. Thromb Res; 1992 Jan 15; 65(2):221-8. PubMed ID: 1579897 [Abstract] [Full Text] [Related]
43. von Willebrand's disease characterized by increased ristocetin sensitivity and the presence of all von Willebrand factor multimers in plasma: a new subtype. Wylie B, Gibson J, Uhr E, Kronenberg H. Pathology; 1988 Jan 15; 20(1):62-3. PubMed ID: 3259690 [Abstract] [Full Text] [Related]
44. A new congenital platelet abnormality characterized by spontaneous platelet aggregation, enhanced von Willebrand factor platelet interaction, and the presence of all von Willebrand factor multimers in plasma. Casonato A, De Marco L, Mazzucato M, De Angelis V, De Roia D, Fabris F, Ruggeri ZM, Girolami A. Blood; 1989 Nov 01; 74(6):2028-33. PubMed ID: 2804346 [Abstract] [Full Text] [Related]
51. Aberrant multimeric structure of von Willebrand factor in a new variant of von Willebrand's disease (type IIC). Ruggeri ZM, Nilsson IM, Lombardi R, Holmberg L, Zimmerman TS. J Clin Invest; 1982 Nov 01; 70(5):1124-7. PubMed ID: 6982283 [Abstract] [Full Text] [Related]
52. Type 2A (IIH) von Willebrand disease is due to mutations that affect von Willebrand factor multimerization. Baronciani L, Federici AB, Punzo M, Solimando M, Cozzi G, La Marca S, Rubini V, Canciani MT, Mannucci PM. J Thromb Haemost; 2009 Jul 01; 7(7):1114-22. PubMed ID: 19422453 [Abstract] [Full Text] [Related]
54. N1421K mutation in the glycoprotein Ib binding domain impairs ristocetin- and botrocetin-mediated binding of von Willebrand factor to platelets. Lanke E, Kristoffersson AC, Isaksson C, Holmberg L, Lethagen S. Eur J Haematol; 2008 Nov 01; 81(5):384-90. PubMed ID: 18637125 [Abstract] [Full Text] [Related]