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.
259 related articles for article (PubMed ID: 2506947)
1. New variant of von Willebrand disease with defective binding to factor VIII. Nishino M; Girma JP; Rothschild C; Fressinaud E; Meyer D Blood; 1989 Oct; 74(5):1591-9. PubMed ID: 2506947 [TBL] [Abstract][Full Text] [Related]
2. A new variant of von Willebrand's disease (type I Padua): doublet-organized plasma von Willebrand factor oligomers in the presence of all size multimers. Casonato A; Pontara E; Dannhäuser D; Bertomoro A; Sartori MT; Girolami A Haematologia (Budap); 1994; 26(2):97-109. PubMed ID: 7890268 [TBL] [Abstract][Full Text] [Related]
3. Further evidence for recessive inheritance of von Willebrand disease with abnormal binding of von Willebrand factor to factor VIII. López-Fernández MF; Blanco-López MJ; Castiñeira MP; Batlle J Am J Hematol; 1992 May; 40(1):20-7. PubMed ID: 1566742 [TBL] [Abstract][Full Text] [Related]
4. Variant von Willebrand disease with defective binding to factor VIII: the first case from Japan. Nishino M; Miura S; Yoshioka A; Kuwahara I; Nishimura T; Hamada K; Fukui H Int J Hematol; 1993 Apr; 57(2):163-73. PubMed ID: 8494994 [TBL] [Abstract][Full Text] [Related]
5. A probable double heterozygous type II von Willebrand's disease with increased ristocetin induced platelet aggregation. Kinoshita S; Yoshioka K; Kasahara M; Takamiya O Am J Hematol; 1992 Jul; 40(3):192-8. PubMed ID: 1609773 [TBL] [Abstract][Full Text] [Related]
6. Diagnosis of von Willebrand disease type 2N: a simplified method for measurement of factor VIII binding to von Willebrand factor. Miller CH; Kelley L; Green D Am J Hematol; 1998 Aug; 58(4):311-8. PubMed ID: 9692396 [TBL] [Abstract][Full Text] [Related]
7. Investigation of a case of subtype IIC von Willebrand disease: characterization of the variability of this subtype. Mazurier C; Mannucci PM; Parquet-Gernez A; Goudemand M; Meyer D Am J Hematol; 1986 Jul; 22(3):301-11. PubMed ID: 3087159 [TBL] [Abstract][Full Text] [Related]
8. Recessive von Willebrand disease type 2 Normandy: variable expression of mild hemophilia and VWD type 1. Michiels JJ; Gadisseur A; Vangenegten I; Schroyens W; Berneman Z Acta Haematol; 2009; 121(2-3):119-27. PubMed ID: 19506358 [TBL] [Abstract][Full Text] [Related]
9. A new von Willebrand factor (vWF) defect in a patient with factor VIII (FVIII) deficiency but with normal levels and multimeric patterns of both plasma and platelet vWF. Characterization of abnormal vWF/FVIII interaction. Mazurier C; Dieval J; Jorieux S; Delobel J; Goudemand M Blood; 1990 Jan; 75(1):20-6. PubMed ID: 2104761 [TBL] [Abstract][Full Text] [Related]
10. Factor VIII:C increases after desmopressin in a subgroup of patients with autosomal recessive severe von Willebrand disease. Castaman G; Lattuada A; Mannucci PM; Rodeghiero F Br J Haematol; 1995 Jan; 89(1):147-51. PubMed ID: 7833254 [TBL] [Abstract][Full Text] [Related]
11. The evaluation of factor VIII binding activity of von Willebrand factor by means of an ELISA method: significance and practical implications. Casonato A; Pontara E; Zerbinati P; Zucchetto A; Girolami A Am J Clin Pathol; 1998 Mar; 109(3):347-52. PubMed ID: 9495210 [TBL] [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 [TBL] [Abstract][Full Text] [Related]
13. High-resolution analysis of von Willebrand factor multimeric composition defines a new variant of type I von Willebrand disease with aberrant structure but presence of all size multimers (type IC). Ciavarella G; Ciavarella N; Antoncecchi S; De Mattia D; Ranieri P; Dent J; Zimmerman TS; Ruggeri ZM Blood; 1985 Dec; 66(6):1423-9. PubMed ID: 3877533 [TBL] [Abstract][Full Text] [Related]
14. Laboratory diagnosis of von Willebrand disease type 1/2E (2A subtype IIE), type 1 Vicenza and mild type 1 caused by mutations in the D3, D4, B1-B3 and C1-C2 domains of the von Willebrand factor gene. Role of von Willebrand factor multimers and the von Willebrand factor propeptide/antigen ratio. Gadisseur A; Berneman Z; Schroyens W; Michiels JJ Acta Haematol; 2009; 121(2-3):128-38. PubMed ID: 19506359 [TBL] [Abstract][Full Text] [Related]
15. Classification and characterization of hereditary types 2A, 2B, 2C, 2D, 2E, 2M, 2N, and 2U (unclassifiable) von Willebrand disease. Michiels JJ; Berneman Z; Gadisseur A; van der Planken M; Schroyens W; van de Velde A; van Vliet H Clin Appl Thromb Hemost; 2006 Oct; 12(4):397-420. PubMed ID: 17000885 [TBL] [Abstract][Full Text] [Related]
16. An Arg760Cys mutation in the consensus sequence of the von Willebrand factor propeptide cleavage site is responsible for a new von Willebrand disease variant. Casonato A; Sartorello F; Cattini MG; Pontara E; Soldera C; Bertomoro A; Girolami A Blood; 2003 Jan; 101(1):151-6. PubMed ID: 12393698 [TBL] [Abstract][Full Text] [Related]
17. von Willebrand's disease: use of collagen binding assay provides potential improvement to laboratory monitoring of desmopressin (DDAVP) therapy. Favaloro EJ; Dean M; Grispo L; Exner T; Koutts J Am J Hematol; 1994 Mar; 45(3):205-11. PubMed ID: 8296790 [TBL] [Abstract][Full Text] [Related]
18. A novel mutation in the D3 domain of von Willebrand factor markedly decreases its ability to bind factor VIII and affects its multimerization. Jorieux S; Gaucher C; Goudemand J; Mazurier C Blood; 1998 Dec; 92(12):4663-70. PubMed ID: 9845532 [TBL] [Abstract][Full Text] [Related]
19. Discrepant increase in factor VIII: C and von Willebrand factor after DDAVP infusion in a patient with variant von Willebrand's disease. Casonato A; Sartori MT; Pontara E; Bertomoro A; Dannhäuser D; Girolami Blood Coagul Fibrinolysis; 1991 Aug; 2(4):567-73. PubMed ID: 1768767 [TBL] [Abstract][Full Text] [Related]
20. Changes in factor VIII binding capacity of von Willebrand factor and factor VIII coagulant activity in two patients with type 2N von Willebrand disease after hemostatic treatment and during pregnancy. Nishino M; Nishino S; Sugimoto M; Shibata M; Tsuji S; Yoshioka A Int J Hematol; 1996 Aug; 64(2):127-34. PubMed ID: 8854570 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]