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Items: 1 to 20 of 122

1.

Biochemistry and genetics of von Willebrand factor.

Sadler JE.

Annu Rev Biochem. 1998;67:395-424. Review.

PMID:
9759493
2.

Correction of a murine model of von Willebrand disease by gene transfer.

Pergolizzi RG, Jin G, Chan D, Pierre L, Bussel J, Ferris B, Leopold PL, Crystal RG.

Blood. 2006 Aug 1;108(3):862-9. Epub 2006 Apr 25.

3.

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.

4.

Molecular genetics of von Willebrand disease.

Mazurier C, Ribba AS, Gaucher C, Meyer D.

Ann Genet. 1998;41(1):34-43. Review.

PMID:
9599650
6.

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
7.

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
8.

Molecular mechanism and classification of von Willebrand disease.

Sadler JE, Matsushita T, Dong Z, Tuley EA, Westfield LA.

Thromb Haemost. 1995 Jul;74(1):161-6. Review.

PMID:
8578450
9.

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. doi: 10.1159/000214852. Epub 2009 Jun 8. Review.

PMID:
19506358
12.

Restoration of plasma von Willebrand factor deficiency is sufficient to correct thrombus formation after gene therapy for severe von Willebrand disease.

De Meyer SF, Vandeputte N, Pareyn I, Petrus I, Lenting PJ, Chuah MK, VandenDriessche T, Deckmyn H, Vanhoorelbeke K.

Arterioscler Thromb Vasc Biol. 2008 Sep;28(9):1621-6. doi: 10.1161/ATVBAHA.108.168369. Epub 2008 Jun 12.

13.

[Von Willebrand's disease].

Furlan M.

Schweiz Med Wochenschr. 1987 Nov 14;117(46):1798-806. Review. German.

PMID:
3122318
14.

A novel von Willebrand factor mutation (I1372S) associated with type 2B-like von Willebrand disease: an elusive phenotype and a difficult diagnosis.

Casonato A, Sartorello F, Pontara E, Gallinaro L, Bertomoro A, Grazia Cattini M, Daidone V, Szukowska M, Pagnan A.

Thromb Haemost. 2007 Dec;98(6):1182-7.

PMID:
18064311
15.
16.

Von Willebrand's disease in the year 2003: towards the complete identification of gene defects for correct diagnosis and treatment.

Castaman G, Federici AB, Rodeghiero F, Mannucci PM.

Haematologica. 2003 Jan;88(1):94-108. Review.

17.

von Willebrand factor and von Willebrand disease.

Ruggeri ZM, Zimmerman TS.

Blood. 1987 Oct;70(4):895-904. Review. Erratum in: Blood 1988 Mar;71(3):830.

18.

Type IIB mutation His-505-->Asp implicates a new segment in the control of von Willebrand factor binding to platelet glycoprotein Ib.

Rabinowitz I, Randi AM, Shindler KS, Tuley EA, Rustagi PK, Sadler JE.

J Biol Chem. 1993 Sep 25;268(27):20497-501.

19.

von Willebrand disease type 2A phenotypes IIC, IID and IIE: A day in the life of shear-stressed mutant von Willebrand factor.

Brehm MA, Huck V, Aponte-Santamaría C, Obser T, Grässle S, Oyen F, Budde U, Schneppenheim S, Baldauf C, Gräter F, Schneider SW, Schneppenheim R.

Thromb Haemost. 2014 Jul 3;112(1):96-108. doi: 10.1160/TH13-11-0902. Epub 2014 Mar 6.

PMID:
24598842
20.

Review article: unexpected bleeding in the operating room: the role of acquired von Willebrand disease.

Lison S, Dietrich W, Spannagl M.

Anesth Analg. 2012 Jan;114(1):73-81. doi: 10.1213/ANE.0b013e318236b16a. Epub 2011 Oct 24. Review.

PMID:
22025497

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