Yvonne V. Sanders

Rotterdam, ZH, Netherlands

Last Updated: 09/26/2026

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Found 14 publications

Women prefer proactive support from providers for treatment of heavy menstrual bleeding: A qualitative study in adult women with moderate or severe Von Willebrand disease.

Women prefer proactive support from providers for treatment of heavy menstrual bleeding: A qualitative study in adult women with moderate or severe Von Willebrand disease.

Journal: Haemophilia : the official journal of the World Federation of Hemophilia

Published: May 31, 2018

Circulating Angiogenic Mediators in Patients with Moderate and Severe von Willebrand Disease: A Multicentre Cross-Sectional Study.

Circulating Angiogenic Mediators in Patients with Moderate and Severe von Willebrand Disease: A Multicentre Cross-Sectional Study.

Journal: Thrombosis and haemostasis

Published: January 06, 2018

Bleeding spectrum in children with moderate or severe von Willebrand disease: Relevance of pediatric-specific bleeding.

Bleeding spectrum in children with moderate or severe von Willebrand disease: Relevance of pediatric-specific bleeding.

Journal: American journal of hematology

Published: July 27, 2015

Joint bleeds in von Willebrand disease patients have significant impact on quality of life and joint integrity: a cross-sectional study.

Joint bleeds in von Willebrand disease patients have significant impact on quality of life and joint integrity: a cross-sectional study.

Journal: Haemophilia : the official journal of the World Federation of Hemophilia

Published: February 20, 2015

Primary postpartum haemorrhage in women with von Willebrand disease or carriership of haemophilia despite specialised care: a retrospective survey.

Primary postpartum haemorrhage in women with von Willebrand disease or carriership of haemophilia despite specialised care: a retrospective survey.

Journal: Haemophilia : the official journal of the World Federation of Hemophilia

Published: December 08, 2014

von Willebrand factor propeptide and the phenotypic classification of von Willebrand disease.

von Willebrand factor propeptide and the phenotypic classification of von Willebrand disease.

Journal: Blood

Published: September 29, 2014

CLEC4M and STXBP5 gene variations contribute to von Willebrand factor level variation in von Willebrand disease.

CLEC4M and STXBP5 gene variations contribute to von Willebrand factor level variation in von Willebrand disease.

Journal: Journal of thrombosis and haemostasis : JTH

Published: July 30, 2014

Von Willebrand disease in the Netherlands: the WiN study

Von Willebrand disease in the Netherlands: the WiN study

Journal: Nederlands tijdschrift voor geneeskunde

Published: May 08, 2014

von Willebrand disease and aging: an evolving phenotype.

von Willebrand disease and aging: an evolving phenotype.

Journal: Journal of thrombosis and haemostasis : JTH

Published: December 18, 2013

Desmopressin response in hemophilia A patients with FVIII:C < 0.10 IU mL(-1.).

Desmopressin response in hemophilia A patients with FVIII:C < 0.10 IU mL(-1.).

Journal: Journal of thrombosis and haemostasis : JTH

Published: August 27, 2013

Reduced prevalence of arterial thrombosis in von Willebrand disease.

Reduced prevalence of arterial thrombosis in von Willebrand disease.

Journal: Journal of thrombosis and haemostasis : JTH

Published: October 12, 2012

Response to desmopressin is strongly dependent on F8 gene mutation type in mild and moderate haemophilia A.

Response to desmopressin is strongly dependent on F8 gene mutation type in mild and moderate haemophilia A.

Journal: Thrombosis and haemostasis

Published: June 11, 2012

Showing 1-12 of 14

Last Updated: 09/26/2026