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Items: 1 to 20 of 56

2.

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
3.

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. Review.

PMID:
16276467
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
5.

Update on the pathophysiology and classification of von Willebrand disease: a report of the Subcommittee on von Willebrand Factor.

Sadler JE, Budde U, Eikenboom JC, Favaloro EJ, Hill FG, Holmberg L, Ingerslev J, Lee CA, Lillicrap D, Mannucci PM, Mazurier C, Meyer D, Nichols WL, Nishino M, Peake IR, Rodeghiero F, Schneppenheim R, Ruggeri ZM, Srivastava A, Montgomery RR, Federici AB; Working Party on von Willebrand Disease Classification.

J Thromb Haemost. 2006 Oct;4(10):2103-14. Epub 2006 Aug 2. Review.

7.

Dominant von Willebrand disease type 2M and 2U are variable expressions of one distinct disease entity caused by loss-of-function mutations in the A1 domain of the von Willebrand factor gene.

Gadisseur A, van der Planken M, Schroyens W, Berneman Z, Michiels JJ.

Acta Haematol. 2009;121(2-3):145-53. doi: 10.1159/000214855. Epub 2009 Jun 8. Review.

PMID:
19506361
8.

Molecular genetics of type 2 von Willebrand disease.

Fressinaud E, Mazurier C, Meyer D.

Int J Hematol. 2002 Jan;75(1):9-18. Review.

PMID:
11843298
9.

The revised classification of von Willebrand disease including the previously masqueraded female hemophilia A (type 2N)

Nishino M, Yoshioka A.

Int J Hematol. 1997 Jul;66(1):21-30. Review. Erratum in: Int J Hematol 1997 Dec;66(4):531.

PMID:
9220657
10.

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. Review.

PMID:
17000885
11.

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
12.

Intravenous DDAVP and factor VIII-von Willebrand factor concentrate for the treatment and prophylaxis of bleedings in patients With von Willebrand disease type 1, 2 and 3.

Michiels JJ, van Vliet HH, Berneman Z, Gadisseur A, van der Planken M, Schroyens W, van der Velden A, Budde U.

Clin Appl Thromb Hemost. 2007 Jan;13(1):14-34. Review.

PMID:
17164493
14.

Molecular basis of von Willebrand disease.

Mazurier C, Meyer D.

Baillieres Clin Haematol. 1996 Jun;9(2):229-41. Review.

PMID:
8800502
15.

Type 2 von Willebrand disease causing defective von Willebrand factor-dependent platelet function.

Meyer D, Fressinaud E, Hilbert L, Ribba AS, Lavergne JM, Mazurier C.

Best Pract Res Clin Haematol. 2001 Jun;14(2):349-64. Review.

PMID:
11686104
16.

Dominant von Willebrand disease type 2A groups I and II due to missense mutations in the A2 domain of the von Willebrand factor gene: diagnosis and management.

Michiels JJ, van Vliet HH.

Acta Haematol. 2009;121(2-3):154-66. doi: 10.1159/000214856. Epub 2009 Jun 8. Review.

PMID:
19506362
17.

Von Willebrand factor and von Willebrand disease.

Budde U, Schneppenheim R.

Rev Clin Exp Hematol. 2001 Dec;5(4):335-68; quiz following 431. Review.

PMID:
11844133
18.

[Information on von Willebrand disease].

Nishino M, Fujimura Y.

Rinsho Byori. 1997 Oct;45(10):942-50. Review. Japanese.

PMID:
9369071
19.

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
20.

von Willebrand disease.

Zimmerman TS, Ruggeri ZM.

Hum Pathol. 1987 Feb;18(2):140-52. Review.

PMID:
3100416
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