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

Jan Michiels; Z Berneman; A Gadisseur; M van der Planken; W Schroyens; A Velde; H van der Vliet

doi:10.1177/1076029606291401

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

Jan Michiels, Z Berneman, A Gadisseur, M van der Planken, W Schroyens, A Velde, H van der Vliet

Research output: Contribution to journal › Article › Academic › peer-review

17 Citations (Scopus)

3 Downloads (Pure)

Original language	Undefined/Unknown
Pages (from-to)	277-295
Number of pages	19
Journal	Clinical & Applied Thrombosis-Hemostasis
Volume	12
Issue number	3
DOIs	https://doi.org/10.1177/1076029606291401
Publication status	Published - 2006

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Michiels, J., Berneman, Z., Gadisseur, A., van der Planken, M., Schroyens, W., Velde, A., & van der Vliet, H. (2006). 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. Clinical & Applied Thrombosis-Hemostasis, 12(3), 277-295. https://doi.org/10.1177/1076029606291401

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title = "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",

author = "Jan Michiels and Z Berneman and A Gadisseur and {van der Planken}, M and W Schroyens and A Velde and {van der Vliet}, H",

year = "2006",

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Michiels, J, Berneman, Z, Gadisseur, A, van der Planken, M, Schroyens, W, Velde, A & van der Vliet, H 2006, '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', Clinical & Applied Thrombosis-Hemostasis, vol. 12, no. 3, pp. 277-295. https://doi.org/10.1177/1076029606291401

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, Jan; Berneman, Z; Gadisseur, A et al.

In: Clinical & Applied Thrombosis-Hemostasis, Vol. 12, No. 3, 2006, p. 277-295.

Research output: Contribution to journal › Article › Academic › peer-review

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AU - Michiels, Jan

AU - Berneman, Z

AU - Gadisseur, A

AU - van der Planken, M

AU - Schroyens, W

AU - Velde, A

AU - van der Vliet, H

PY - 2006

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DO - 10.1177/1076029606291401

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Michiels J, Berneman Z, Gadisseur A, van der Planken M, Schroyens W, Velde A et al. 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. Clinical & Applied Thrombosis-Hemostasis. 2006;12(3):277-295. doi: 10.1177/1076029606291401