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Journal Articles

Wish-Qol Study - Assessment of Health-Related Quality of Life (HRQoL) and Health-Economic Aspects in Patients with Von Willebrand Disease (VWD) in France: Results of the Women Cohort

Annie Borel-Derlon, MD PhD, Jenny Goudemand, MD PhD, Dominique Desprez, MD, Fabienne Volot, MD, Yves Gruel, MD, Sophie Bayard, MD, Catherine Chatelanaz, Catherine Doriat-Robin, Agnes Veyradier, MD PhD, Edith Fressinaud, MD, Sylvia von Mackensen, PhD

Blood (2016) 128 (22): 1395.

https://doi.org/10.1182/blood.V128.22.1395.1395

Published: 2016

Journal Articles

Mutations in the A3 domain of Von Willebrand factor inducing combined qualitative and quantitative defects in the protein

Paulette Legendre, Ana-Maria Navarrete, Julie Rayes, Caterina Casari, Pierre Boisseau, Catherine Ternisien, Claudine Caron, Edith Fressinaud, Jenny Goudemand, Agnès Veyradier, Cécile V. Denis, Peter J. Lenting, Olivier D. Christophe

Blood (2013) 121 (11): 2135–2143.

https://doi.org/10.1182/blood-2012-09-456038

Published: 2013

Includes: Supplemental data

Journal Articles

First Case of Platelet-Type Von Willebrand Disease (PT-VWD) Associated with Type 2B Von Willebrand Disease (2B VWD)

Marie Dreyfus, Celine Desconclois, Corinne Guitton, Marie-Jeanne Baas, Helene Mandard, Pierre Boisseau, Jenny Goudemand, MD, PhD, Claudine Caron, Nathalie Itzhar, Agnes Veyradier, Francois Lanza, PhD, MD, Edith Fressinaud

Blood (2011) 118 (21): 5313.

https://doi.org/10.1182/blood.V118.21.5313.5313

Published: 2011

Journal Articles

Response to desmopressin is influenced by the genotype and phenotype in type 1 von Willebrand disease (VWD): results from the European Study MCMDM-1VWD

Blood (2008) 111 (7): 3531–3539.

https://doi.org/10.1182/blood-2007-08-109231

Published: 2008

Includes: Supplemental data

Journal Articles

O -Linked Glycosylation with Sialylated T-Antigen: A Novel Carbohydrate Determinant of von Willebrand Factor Antigen Levels.

Peter J. Lenting, PhD, Carina J.M. van Schooten, MSc, Ton Lisman, PhD, Marijke van den Berg, MD, PhD, Jeroen C.J. Eikenboom, MD, PhD, Frank W.G. Leebeek, MD, PhD, Jenny Goudemand, MD, PhD, Edith Fressinaud, MD, PhD, Philip G. de Groot, PhD, Cécile V. Denis, PhD

Blood (2006) 108 (11): 178.

https://doi.org/10.1182/blood.V108.11.178.178

Published: 2006

Journal Articles

Variations in glycosylation of von Willebrand factor with O -linked sialylated T antigen are associated with its plasma levels

Carina J. M. van Schooten, Cécile V. Denis, Ton Lisman, Jeroen C. J. Eikenboom, Frank W. Leebeek, Jenny Goudemand, Edith Fressinaud, H. Marijke van den Berg, Philip G. de Groot, Peter J. Lenting

Blood (2006) 109 (6): 2430–2437.

https://doi.org/10.1182/blood-2006-06-032706

Published: 2006

Journal Articles

Impaired megakaryocytopoiesis in type 2B von Willebrand disease with severe thrombocytopenia

Paquita Nurden, Najet Debili, William Vainchenker, Regis Bobe, Raymonde Bredoux, Elisabeth Corvazier, Robert Combrie, Edith Fressinaud, Dominique Meyer, Alan T. Nurden, Jocelyne Enouf

Blood (2006) 108 (8): 2587–2595.

https://doi.org/10.1182/blood-2006-03-009449

Published: 2006

Includes: Supplemental data

Journal Articles

FranceCoag Network: A National Multicenter Prospective Cohort for Congenital Bleeding Disorders.

Edith Fressinaud, Jocelyne Dieval, Valerie Gay, Viviane Guerin, Thierry Lambert, Jean Donadieu, Reseau FranceCoag

Blood (2005) 106 (11): 4094.

https://doi.org/10.1182/blood.V106.11.4094.4094

Published: 2005

Journal Articles

Immune Tolerance with a High Purity Plasma Derived Factor VIII Containing Von Willebrand Factor in Haemophilia A Patients with High Responding Inhibitors.

Benoit Polack, MD, PhD, Philippe Beurrier, MD, Chantal Rothschild, MD, Frédérique Orsini, Albert Faradji, MD, Anne Liennhard, MD, Edith Fressinaud, MD, PhD, Jenny Goudemand, MD

Blood (2004) 104 (11): 3096.

https://doi.org/10.1182/blood.V104.11.3096.3096

Published: 2004

Journal Articles

A point mutation in the cysteine-rich domain of glycoprotein (GP) IIIa results in the expression of a GPIIb-IIIa (αIIbβ3) integrin receptor locked in a high-affinity state and a Glanzmann thrombasthenia–like phenotype

Catherine Ruiz, Chao-Yan Liu, Qi-Hong Sun, Marianne Sigaud-Fiks, Edith Fressinaud, Jean-Yves Muller, Paquita Nurden, Alan T. Nurden, Peter J. Newman, Nathalie Valentin

Blood (2001) 98 (8): 2432–2441.

https://doi.org/10.1182/blood.V98.8.2432

Published: 2001

Journal Articles

The arginine-552-cysteine (R1315C) mutation within the A1 loop of von Willebrand factor induces an abnormal folding with a loss of function resulting in type 2A–like phenotype of von Willebrand disease: study of 10 patients and mutated recombinant von Willebrand factor

Anne-Sophie Ribba, Lysiane Hilbert, Jean-Maurice Lavergne, Edith Fressinaud, Catherine Boyer-Neumann, Catherine Ternisien, Irène Juhan-Vague, Jenny Goudemand, Jean-Pierre Girma, Claudine Mazurier, Dominique Meyer

Blood (2001) 97 (4): 952–959.

https://doi.org/10.1182/blood.V97.4.952

Published: 2001

Journal Articles

Somatic mosaicism and compound heterozygosity in female hemophilia B

Jean-Marc Costa, Dominique Vidaud, Ingrid Laurendeau, Michel Vidaud, Edith Fressinaud, Jean-Pierre Moisan, Albert David, Dominique Meyer, Jean-Maurice Lavergne

Blood (2000) 96 (4): 1585–1587.

https://doi.org/10.1182/blood.V96.4.1585

Published: 2000

Journal Articles

Conformational changes in the D′ domain of von Willebrand factor induced by CYS 25 and CYS 95 mutations lead to factor VIII binding defect and multimeric impairment

Sylvie Jorieux, Edith Fressinaud, Jenny Goudemand, Christine Gaucher, Dominique Meyer, Claudine Mazurier, the INSERM Network on Molecular Abnormalities in von Willebrand Disease

Blood (2000) 95 (10): 3139–3145.

https://doi.org/10.1182/blood.V95.10.3139

Published: 2000

Journal Articles

Screening for von Willebrand Disease With a New Analyzer Using High Shear Stress: A Study of 60 Cases

Edith Fressinaud, Agnès Veyradier, Florence Truchaud, Isabelle Martin, Catherine Boyer-Neumann, Marc Trossaert, Dominique Meyer

Blood (1998) 91 (4): 1325–1331.

https://doi.org/10.1182/blood.V91.4.1325

Published: 1998

NARROW

Wish-Qol Study - Assessment of Health-Related Quality of Life (HRQoL) and Health-Economic Aspects in Patients with Von Willebrand Disease (VWD) in France: Results of the Women Cohort

Mutations in the A3 domain of Von Willebrand factor inducing combined qualitative and quantitative defects in the protein

First Case of Platelet-Type Von Willebrand Disease (PT-VWD) Associated with Type 2B Von Willebrand Disease (2B VWD)

Response to desmopressin is influenced by the genotype and phenotype in type 1 von Willebrand disease (VWD): results from the European Study MCMDM-1VWD

O -Linked Glycosylation with Sialylated T-Antigen: A Novel Carbohydrate Determinant of von Willebrand Factor Antigen Levels.

Variations in glycosylation of von Willebrand factor with O -linked sialylated T antigen are associated with its plasma levels

Impaired megakaryocytopoiesis in type 2B von Willebrand disease with severe thrombocytopenia

FranceCoag Network: A National Multicenter Prospective Cohort for Congenital Bleeding Disorders.

Immune Tolerance with a High Purity Plasma Derived Factor VIII Containing Von Willebrand Factor in Haemophilia A Patients with High Responding Inhibitors.

A point mutation in the cysteine-rich domain of glycoprotein (GP) IIIa results in the expression of a GPIIb-IIIa (αIIbβ3) integrin receptor locked in a high-affinity state and a Glanzmann thrombasthenia–like phenotype

The arginine-552-cysteine (R1315C) mutation within the A1 loop of von Willebrand factor induces an abnormal folding with a loss of function resulting in type 2A–like phenotype of von Willebrand disease: study of 10 patients and mutated recombinant von Willebrand factor

Somatic mosaicism and compound heterozygosity in female hemophilia B

Conformational changes in the D′ domain of von Willebrand factor induced by CYS 25 and CYS 95 mutations lead to factor VIII binding defect and multimeric impairment

Screening for von Willebrand Disease With a New Analyzer Using High Shear Stress: A Study of 60 Cases

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American Society of Hematology

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