These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
128 related articles for article (PubMed ID: 9681234)
21. Multiple von Willebrand factor mutations in patients with recessive type 1 von Willebrand disease. Casonato A; Gallinaro L; Pontara E; Bernardo L; Sartorello F; Daidone V; Pagnan A Thromb Res; 2007; 120(3):451-3. PubMed ID: 17157361 [No Abstract] [Full Text] [Related]
22. von Willebrand's variants. Ludlam CA; Steel CM Lancet; 1993 Apr; 341(8851):997. PubMed ID: 8096952 [No Abstract] [Full Text] [Related]
23. The rapid differentiation of type IIb von Willebrand's disease from platelet-type (pseudo-) von Willebrand's disease by the "neutral" monoclonal antibody binding assay. Scott JP; Montgomery RR Am J Clin Pathol; 1991 Dec; 96(6):723-8. PubMed ID: 1746488 [TBL] [Abstract][Full Text] [Related]
24. [Intermittent thrombocytopenia as a manifestation of Von Willebrand's disease]. Gómez García EB; Brouwers GJ; Kappers-Klunne MC; Leebeek FW; van Vliet HH Ned Tijdschr Geneeskd; 2002 Jun; 146(25):1192-5. PubMed ID: 12109311 [TBL] [Abstract][Full Text] [Related]
25. Diagnostic and therapeutic difficulties in type 2A von Willebrand disease: resolution. Thomas MR; Cutler JA; Savidge GF Clin Appl Thromb Hemost; 2006 Apr; 12(2):237-9. PubMed ID: 16708129 [TBL] [Abstract][Full Text] [Related]
27. Laboratory diagnosis of von Willebrand's disease. Triplett DA Mayo Clin Proc; 1991 Aug; 66(8):832-40. PubMed ID: 1907342 [TBL] [Abstract][Full Text] [Related]
28. von Willebrand disease, type 2B: A diagnosis more elusive than previously thought. Favaloro EJ Thromb Haemost; 2008 Mar; 99(3):630-1; author reply 632-3. PubMed ID: 18327414 [No Abstract] [Full Text] [Related]
29. Gastrointestinal angiodysplasia in a patient with type 2 von Willebrand's disease and analysis of exon 28 of the von Willebrand factor gene. Satoh Y; Kita H; Kihira K; Mutoh H; Osawa H; Satoh K; Ido K; Sakata Y; Sugano K Am J Gastroenterol; 2004 Dec; 99(12):2495-8. PubMed ID: 15571600 [TBL] [Abstract][Full Text] [Related]
30. Von Willebrand's disease. Ewenstein BM Annu Rev Med; 1997; 48():525-42. PubMed ID: 9046981 [TBL] [Abstract][Full Text] [Related]
31. Clinical profile of the association of P.R1205h and P.R924q in a patient with von Willebrand's disease. Woods AI; Kempfer AC; Sánchez-Luceros A; Calderazzo JC; Grosso SH; Lazzari MA Haemophilia; 2013 May; 19(3):e180-1. PubMed ID: 23490306 [No Abstract] [Full Text] [Related]
32. Molecular and clinical profile of von Willebrand disease in Spain (PCM-EVW-ES): Proposal for a new diagnostic paradigm. Batlle J; Pérez-Rodríguez A; Corrales I; López-Fernández MF; Rodríguez-Trillo Á; Lourés E; Cid AR; Bonanad S; Cabrera N; Moret A; Parra R; Mingot-Castellano ME; Balda I; Altisent C; Pérez-Montes R; Fisac RM; Iruín G; Herrero S; Soto I; de Rueda B; Jiménez-Yuste V; Alonso N; Vilariño D; Arija O; Campos R; Paloma MJ; Bermejo N; Toll T; Mateo J; Arribalzaga K; Marco P; Palomo Á; Sarmiento L; Iñigo B; Nieto Mdel M; Vidal R; Martínez MP; Aguinaco R; César JM; Ferreiro M; García-Frade J; Rodríguez-Huerta AM; Cuesta J; Rodríguez-González R; García-Candel F; Cornudella R; Aguilar C; Borràs N; Vidal F Thromb Haemost; 2016 Jan; 115(1):40-50. PubMed ID: 26245874 [TBL] [Abstract][Full Text] [Related]
33. Discrepancies between von Willebrand factor multimeric composition and other tests in some von Willebrand's disease variants. Casonato A; Fabris F; De Marco L; Girolami A Blut; 1987 Jul; 55(1):61-2. PubMed ID: 3496930 [No Abstract] [Full Text] [Related]
34. Characterization of the von Willebrand factor gene (VWF) in von Willebrand disease type III patients from 24 families of Swedish and Finnish origin. Zhang ZP; Blombäck M; Egberg N; Falk G; Anvret M Genomics; 1994 May; 21(1):188-93. PubMed ID: 8088787 [TBL] [Abstract][Full Text] [Related]
35. Von Willebrand's disease: a novel mutation, P1824H and the incidence of R1205H defect among families with dominant quantitative von Willebrand factor deficiency. Casaña P; Cabrera N; Haya S; Cid AR; Aznar JA Haematologica; 2006 Aug; 91(8):1130-3. PubMed ID: 16870550 [TBL] [Abstract][Full Text] [Related]
36. Classification of variant von Willebrand's disease subtypes by analysis of functional characteristics and multimeric composition of factor VIII/von Willebrand factor. Ruggeri ZM; Zimmerman TS Ann N Y Acad Sci; 1981; 370():205-9. PubMed ID: 6791543 [No Abstract] [Full Text] [Related]
37. Mutations in severe, type III von Willebrand's disease in the Dutch population: candidate missense and nonsense mutations associated with reduced levels of von Willebrand factor messenger RNA. Eikenboom JC; Ploos van Amstel HK; Reitsma PH; Briët E Thromb Haemost; 1992 Oct; 68(4):448-54. PubMed ID: 1448779 [TBL] [Abstract][Full Text] [Related]
38. Electroblot and immunoperoxidase staining for rapid screening of the abnormalities of the multimeric structure of von Willebrand factor in von Willebrand's disease. Lombardi R; Gelfi C; Righetti PG; Lattuada A; Mannucci PM Thromb Haemost; 1986 Apr; 55(2):246-9. PubMed ID: 3520937 [TBL] [Abstract][Full Text] [Related]
40. A new candidate mutation (N528S) within the von Willebrand factor propeptide identified in a Japanese patient with phenotype IIC of von Willebrand disease. Gaucher C; Uno H; Yamazaki T; Mashiba H; Mazurier C Eur J Haematol; 1998 Aug; 61(2):145-8. PubMed ID: 9714529 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]