219 related articles for article (PubMed ID: 9569179)
21. [Molecular study of type 2 von Willebrand disease].
Habart D; Smejkal P; Matýsková M; Turek P; Hrachovinová I; Vorlová Z
Cas Lek Cesk; 2003; 142(6):373-6. PubMed ID: 12924038
[TBL] [Abstract][Full Text] [Related]
22. 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]
23. A common splice site mutation is shared by two families with different type 2N von Willebrand disease mutations.
Nesbitt IM; Hampton KK; Preston FE; Peake IR; Goodeve AC
Thromb Haemost; 1999 Sep; 82(3):1061-4. PubMed ID: 10494764
[TBL] [Abstract][Full Text] [Related]
24. Von Willebrand's disease caused by compound heterozygosity for a substitution mutation (T1156M) in the D3 domain of the von Willebrand factor and a stop mutation (Q2470X).
Lethagen S; Isaksson C; Schaedel C; Holmberg L
Thromb Haemost; 2002 Sep; 88(3):421-6. PubMed ID: 12353070
[TBL] [Abstract][Full Text] [Related]
25. Mutations in von Willebrand factor multimerization domains are not a common cause of classical type 1 von Willebrand disease.
Keeney S; Cumming A; Hay C
Thromb Haemost; 1999 Nov; 82(5):1446-50. PubMed ID: 10595636
[TBL] [Abstract][Full Text] [Related]
26. Expression of two type 2N von Willebrand disease mutations identified in exon 18 of von Willebrand factor gene.
Hilbert L; Jorieux S; Fontenay-Roupie M; Guicheteau M; Fressinaud E; Meyer D; Mazurier C;
Br J Haematol; 2004 Oct; 127(2):184-9. PubMed ID: 15461624
[TBL] [Abstract][Full Text] [Related]
27. 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; 112(5-6):291-5. PubMed ID: 15041272
[TBL] [Abstract][Full Text] [Related]
28. 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
[TBL] [Abstract][Full Text] [Related]
29. Impaired dimerization of von Willebrand factor subunit due to mutation A2801D in the CK domain results in a recessive type 2A subtype IID von Willebrand disease.
Hommais A; Stépanian A; Fressinaud E; Mazurier C; Pouymayou K; Meyer D; Girma JP; Ribba AS
Thromb Haemost; 2006 May; 95(5):776-81. PubMed ID: 16676067
[TBL] [Abstract][Full Text] [Related]
30. Autosomal recessive von Willebrand disease type 1 or 2 due to homozygous or compound heterozygous mutations in the von Willebrand factor gene. A single center experience on molecular heterogeneity and laboratory features in 12 families.
Castaman G; Giacomelli S; Rodeghiero F
Acta Haematol; 2009; 121(2-3):106-10. PubMed ID: 19506356
[TBL] [Abstract][Full Text] [Related]
31. Von Willebrand disease - phenotype versus genotype: deficiency versus disease.
Lillicrap D
Thromb Res; 2007; 120 Suppl 1():S11-6. PubMed ID: 17490730
[TBL] [Abstract][Full Text] [Related]
32. Characterization of von Willebrand factor gene defects in two unrelated patients with type IIC von Willebrand disease.
Gaucher C; Diéval J; Mazurier C
Blood; 1994 Aug; 84(4):1024-30. PubMed ID: 8049421
[TBL] [Abstract][Full Text] [Related]
33. [Mutation (Ala737-->Glu) in type 2A von Willebrand disease].
Wang Y; Zhang J; Wan H
Zhonghua Xue Ye Xue Za Zhi; 1999 Mar; 20(3):117-9. PubMed ID: 11601234
[TBL] [Abstract][Full Text] [Related]
34. A von Willebrand's factor genomic nucleotide variant and polymerase chain reaction diagnostic test associated with inheritable type-2 von Willebrand's disease in a line of german shorthaired pointer dogs.
Kramer JW; Venta PJ; Klein SR; Cao Y; Schall WD; Yuzbasiyan-Gurkan V
Vet Pathol; 2004 May; 41(3):221-8. PubMed ID: 15133170
[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. 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]
37. Compound heterozygosity for two novel mutations (1203insG/Y1456X) in the von Willebrand factor gene causing type 3 von Willebrand disease.
Xie F; Wang X; Cooper DN; Lan F; Fang Y; Cai X; Wang Z; Wang H
Haemophilia; 2007 Sep; 13(5):645-8. PubMed ID: 17880457
[TBL] [Abstract][Full Text] [Related]
38. Laboratory diagnosis and molecular basis of mild von Willebrand disease type 1.
Michiels JJ; Berneman Z; Gadisseur A; van der Planken M; Schroyens W; van Vliet HH
Acta Haematol; 2009; 121(2-3):85-97. PubMed ID: 19506353
[TBL] [Abstract][Full Text] [Related]
39. [Study on genetic mutations of the vWF in type 2A von Willebrand disease].
Wang Y; Zhang J; Zhang W; Cheng D; Wan H; Ruan C
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2000 Aug; 17(4):229-32. PubMed ID: 10932002
[TBL] [Abstract][Full Text] [Related]
40. Diagnosis of inherited von Willebrand disease: a clinical perspective.
Federici AB
Semin Thromb Hemost; 2006 Sep; 32(6):555-65. PubMed ID: 16977566
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
