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Items: 1 to 20 of 90

1.

VWF sequence variants: innocent until proven guilty.

Babushok D, Cuker A.

Blood. 2012 Mar 1;119(9):1959-60. doi: 10.1182/blood-2012-01-403634.

2.

Characterization of recessive severe type 1 and 3 von Willebrand Disease (VWD), asymptomatic heterozygous carriers versus bloodgroup O-related von Willebrand factor deficiency, and dominant type 1 VWD.

Michiels JJ, Berneman Z, Gadisseur A, van der Planken M, Schroyens W, van de Velde A, van Vliet H.

Clin Appl Thromb Hemost. 2006 Jul;12(3):277-95. Review.

PMID:
16959681
5.
6.

New variant of type II von Willebrand's disease with structural abnormality of plasma von Willebrand factor in a patient with very mild bleeding history.

Baillod P, Gaucher C, Affolter B, Mazurier C, Pflugshaupt R.

Am J Hematol. 1995 May;49(1):21-8. Review.

PMID:
7741134
7.

Laboratory diagnosis and molecular classification of von Willebrand disease.

Gadisseur A, Hermans C, Berneman Z, Schroyens W, Deckmyn H, Michiels JJ.

Acta Haematol. 2009;121(2-3):71-84. doi: 10.1159/000214846. Epub 2009 Jun 8. Review.

PMID:
19506352
8.

Proteolytic processing of von Willebrand factor subunit: heterogeneity in type-IIA von Willebrand disease.

Batlle J, Lasierra J, Villamor AF, Navarro JL, Pardo A, Campos M, Justiça B, López Fernández MF.

Ann Hematol. 1994 Mar;68(3):111-5.

PMID:
8167176
9.

Type 2M von Willebrand disease: F606I and I662F mutations in the glycoprotein Ib binding domain selectively impair ristocetin- but not botrocetin-mediated binding of von Willebrand factor to platelets.

Hillery CA, Mancuso DJ, Evan Sadler J, Ponder JW, Jozwiak MA, Christopherson PA, Cox Gill J, Paul Scott J, Montgomery RR.

Blood. 1998 Mar 1;91(5):1572-81.

10.

Von Willebrand disease - phenotype versus genotype: deficiency versus disease.

Lillicrap D.

Thromb Res. 2007;120 Suppl 1:S11-6. Epub 2007 May 8. Review.

PMID:
17490730
11.

Determinants of bleeding severity in von Willebrand disease.

Di Paola J.

Curr Hematol Rep. 2005 Sep;4(5):345-9.

PMID:
16131434
12.

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.

PMID:
7890268
13.
14.

Diagnosis of subtype 2B von Willebrand disease in a patient with 2A phenotype of plasma von Willebrand factor.

Gaucher C, de Romeuf C, Rauïs-Morret M, Corazza F, Fondu P, Mazurier C.

Thromb Haemost. 1995 Apr;73(4):610-6.

PMID:
7495067
15.

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 1;101(1):151-6. Epub 2002 Aug 8.

16.

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.

PMID:
1566742
20.

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