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É. Fressinaud · SciRah

Researcher profile · Semantic Scholar

É. Fressinaud

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É. Fressinaud — researcher profile on SciRah

h-index: 43
Works: 122
Citations: 6,729

Most-cited papers

Platelet Factor 4 Complexed to Heparin Is the Target for Antibodies Generated in Heparin-Induced Thrombocytopenia
J. Amiral, F. Bridey, M. Dreyfus, A. Vissac +3 more
1992Thrombosis and Haemostasis738 citations
Semantic Scholar
A quantitative analysis of bleeding symptoms in type 1 von Willebrand disease: results from a multicenter European study (MCMDM‐1 VWD)
A. Tosetto, F. Rodeghiero, G. Castaman, A. Goodeve +17 more
2006Journal of Thrombosis and Haemostasis558 citations Open access
Semantic Scholar
Screening for von Willebrand disease with a new analyzer using high shear stress: a study of 60 cases.
É. Fressinaud, A. Veyradier, F. Truchaud, Isabelle Martin +3 more
1998Blood342 citations
Semantic Scholar
Antibodies to Macromolecular Platelet Factor 4-Heparin Complexes in Heparin-induced Thrombocytopenia: a Study of 44 Cases
J. Amiral, F. Bridey, M. Wolf, C. Boyer-Neumann +5 more
1995Thrombosis and Haemostasis297 citations
Semantic Scholar
Presence of autoantibodies to interleukin-8 or neutrophil-activating peptide-2 in patients with heparin-associated thrombocytopenia.
J. Amiral, A. Marfaing-Koka, M. Wolf, M. Alessi +6 more
1996Blood231 citations
Semantic Scholar
Response to desmopressin is influenced by the genotype and phenotype in type 1 von Willebrand disease (VWD): results from the European Study MCMDM-1VWD.
G. Castaman, S. Lethagen, A. Federici, A. Tosetto +17 more
2008Blood210 citations Open access
Semantic Scholar
Scott syndrome, characterized by impaired transmembrane migration of procoagulant phosphatidylserine and hemorrhagic complications, is an inherited disorder.
Florence Toti, N. Satta, É. Fressinaud, Dominique Meyer +1 more
1996Blood208 citations
Semantic Scholar
High incidence of anti‐heparin/platelet factor 4 antibodies after cardiopulmonary bypass surgery
M. Trossaërt, Anne Gaillard, P. Commin, J. Amiral +2 more
1998British Journal of Haematology150 citations Open access
Semantic Scholar
Acquired von Willebrand Syndrome: from Pathophysiology to Management
A. Veyradier, CharlesS. P Jenkins, É. Fressinaud, D. Meyer
2000Thrombosis and Haemostasis130 citations
Semantic Scholar
International Survey of Patients with von Willebrand Disease and Angiodysplasia
É. Fressinaud, D. Meyer
1993Thrombosis and Haemostasis127 citations
Semantic Scholar
Gene Defects in 150 Unrelated French Cases with Type 2 von Willebrand Disease: from the Patient to the Gene
D. Meyer, É. Fressinaud, C. Gaucher, J. Lavergne +4 more
1997Thrombosis and Haemostasis125 citations
Semantic Scholar
Intracranial haemorrhages in French haemophilia patients (1991–2001): clinical presentation, management and prognosis factors for death
N. Stieltjes, T. Calvez, V. Demiguel, M. Torchet +5 more
2005Haemophilia124 citations
Semantic Scholar
Type 2N von Willebrand disease: clinical manifestations, pathophysiology, laboratory diagnosis and molecular biology.
C. Mazurier, J. Goudemand, L. Hilbert, C. Caron +2 more
2001Baillière's Best Practice & Research: Clinical Haematology124 citations
Semantic Scholar
Estimation of the von Willebrand Factor-cleaving Protease in Plasma Using Monoclonal Antibodies to vWF
B. Obert, H. Tout, A. Veyradier, É. Fressinaud +2 more
1999Thrombosis and Haemostasis122 citations
Semantic Scholar
Use of Recombinant Factor VIIa in 3 Patients with Inherited Type I Glanzmann’s Thrombasthenia Undergoing Invasive Procedures
R. d'Oiron, C. Menart, M. Trzeciak, P. Nurden +4 more
2000Thrombosis and Haemostasis118 citations
Semantic Scholar
Management of dental extractions in patients with bleeding disorders.
B. Piot, M. Sigaud-Fiks, P. Huet, É. Fressinaud +2 more
2002Oral surgery, oral medicine, oral pathology, oral radiology, and endodontics103 citations
Semantic Scholar
Mild hemophilia A with factor VIII assay discrepancy: using thrombin generation assay to assess the bleeding phenotype
M. Trossaert, V. Regnault, M. Sigaud, P. Boisseau +2 more
2008Journal of Thrombosis and Haemostasis100 citations Open access
Semantic Scholar
Mapping of X-linked myxomatous valvular dystrophy to chromosome Xq28.
F. Kyndt, J. Schott, J. Trochu, Florence Baranger +8 more
1998American Journal of Human Genetics100 citations Open access
Semantic Scholar
Variations in glycosylation of von Willebrand factor with O-linked sialylated T antigen are associated with its plasma levels.
Carina J. M. van Schooten, C. Denis, T. Lisman, Jeroen Eikenboom +6 more
2007Blood93 citations Open access
Semantic Scholar
Impaired megakaryocytopoiesis in type 2B von Willebrand disease with severe thrombocytopenia.
P. Nurden, N. Debili, W. Vainchenker, R. Bobe +7 more
2006Blood91 citations
Semantic Scholar
Therapeutic monitoring of von Willebrand disease: interest and limits of a platelet function analyser at high shear rates
É. Fressinaud, A. Veyradier, M. Sigaud, C. Boyer-Neumann +2 more
1999British Journal of Haematology88 citations Open access
Semantic Scholar
Use of recombinant factor VIIa (NovoSeven) in patients with Glanzmann thrombasthenia.
Man-Chiu Poon, R. d'Oiron, I. Hann, C. Négrier +37 more
2001Seminars in hematology (Print)85 citations
Semantic Scholar
Aminophospholipid exposure, microvesiculation and abnormal protein tyrosine phosphorylation in the platelets of a patient with Scott syndrome: a study using physiologic agonists and local anaesthetics
J. Dachary‐Prigent, J. Pasquet, É. Fressinaud, F. Toti +2 more
1997British Journal of Haematology75 citations Open access
Semantic Scholar
Molecular basis of severe factor XI deficiency in seven families from the west of France. Seven novel mutations, including an ancient Q88X mutation
F. Quélin, M. Trossaert, M. Sigaud, P. Mazancourt +1 more
2004Journal of Thrombosis and Haemostasis72 citations Open access
Semantic Scholar
A Laboratory Phenotype/Genotype Correlation of 1167 French Patients From 670 Families With von Willebrand Disease
A. Veyradier, P. Boisseau, É. Fressinaud, C. Caron +12 more
2016Medicine70 citations Open access
Semantic Scholar
Expression of 14 von Willebrand factor mutations identified in patients with type 1 von Willebrand disease from the MCMDM‐1VWD study
J. Eikenboom, L. Hilbert, A. Ribba, A. Hommais +24 more
2009Journal of Thrombosis and Haemostasis68 citations Open access
Semantic Scholar
Shear rate-dependent impairment of thrombus growth on collagen in nonanticoagulated blood from patients with von Willebrand disease and hemophilia A.
É. Fressinaud, K. Sakariassen, Chantal Rothschild, H. R. Baumgartner +1 more
1992Blood68 citations Open access
Semantic Scholar
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.
S. Jorieux, É. Fressinaud, Jenny Goudemand, C. Gaucher +2 more
2000Blood61 citations
Semantic Scholar
A point mutation in the cysteine-rich domain of glycoprotein (GP) IIIa results in the expression of a GPIIb-IIIa (alphaIIbbeta3) 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 +6 more
2001Blood57 citations
Semantic Scholar
Type 2 von Willebrand disease causing defective von Willebrand factor-dependent platelet function.
Dominique Meyer, É. Fressinaud, L. Hilbert, A. Ribba +2 more
2001Baillière's Best Practice & Research: Clinical Haematology52 citations
Semantic Scholar
Scott syndrome: an inherited defect of the procoagulant activity of platelets.
N. Satta, F. Toti, É. Fressinaud, D. Meyer +1 more
1997Platelets52 citations
Semantic Scholar
Incidence of Factor VIII Inhibitor Development in Severe Hemophilia A Patients Treated only with One Brand of Highly Purified Plasma-Derived Concentrate
C. Guérois, Y. Laurian, C. Rothschild, A. Parquet‐Gernez +10 more
1995Thrombosis and Haemostasis52 citations
Semantic Scholar
Iliopsoas hematoma in patients with hemophilia: a single-center study.
M. Dauty, M. Sigaud, M. Trossaërt, É. Fressinaud +2 more
2007Joint, bone, spine : revue du rhumatisme48 citations
Semantic Scholar
The role of platelet von Willebrand factor in platelet adhesion and thrombus formation: a study of 34 patients with various subtypes of type I von Willebrand disease
É. Fressinaud, Augusto B. Federici, G. Castaman, C. Rothschild +4 more
1994British Journal of Haematology45 citations
Semantic Scholar
Two novel mutations, Q1053H and C1060R, located in the D3 domain of von Willebrand factor, are responsible for decreased FVIII‐binding capacity
L. Hilbert, S. Jorieux, V. Proulle, R. Favier +5 more
2003British Journal of Haematology44 citations
Semantic Scholar
Significance of capacitative Ca2+ entry in the regulation of phosphatidylserine expression at the surface of stimulated cells.
Maria Martinez, Sophie Martin, Florence Toti, É. Fressinaud +3 more
1999Biochemistry44 citations
Semantic Scholar
von Willebrand factor mutation promotes thrombocytopathy by inhibiting integrin αIIbβ3.
C. Casari, E. Berrou, M. Lebret, F. Adam +9 more
2013Journal of Clinical Investigation42 citations Open access
Semantic Scholar
Platelet function analyser (PFA‐100) results and von Willebrand factor deficiency: a 16‐year ‘real‐world’ experience
L. Ardillon, C. Ternisien, M. Fouassier, M. Sigaud +6 more
2015Haemophilia41 citations
Semantic Scholar
Protein A Sepharose immunoadsorption can restore the efficacy of platelet concentrates in patients with Glanzmann's thrombasthenia and anti‐glycoprotein IIb–IIIa antibodies
I. Martin, F. Kriaa, V. Proulle, B. Guillet +9 more
2002British Journal of Haematology38 citations
Semantic Scholar
Detection of a molecular defect in 40 of 44 patients with haemophilia B by PCR and denaturing gradient gel electrophoresis
Michel Tartary, D. Vidaud, Ying-Chao Piao, Jean-marc Costa +7 more
1993British Journal of Haematology38 citations
Semantic Scholar
Type 2N von Willebrand disease due to compound heterozygosity for R854Q and a novel R763G mutation at the cleavage site of von Willebrand factor propeptide
L. Hilbert, P. Nurden, C. Caron, A. Nurden +4 more
2006Thrombosis and Haemostasis37 citations
Semantic Scholar
Molecular Genetics of Type 2 von Willebrand Disease
É. Fressinaud, C. Mazurier, D. Meyer
2002International journal of hematology37 citations
Semantic Scholar
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.
A. Ribba, L. Hilbert, J. Lavergne, É. Fressinaud +7 more
2001Blood36 citations
Semantic Scholar
A New Automated Method for von Willebrand Factor Antigen Measurement Using Latex Particles
Agnès Veyradier, É. Fressinaud, M. Sigaud, M. Wolf +1 more
1999Thrombosis and Haemostasis36 citations
Semantic Scholar
Validation of the first commercial ELISA for type 2N von Willebrand’s disease diagnosis
A. Veyradier, C. Caron, C. Ternisien, M. Wolf +3 more
2011Haemophilia30 citations
Semantic Scholar
Mutations in the A3 domain of von Willebrand factor inducing combined qualitative and quantitative defects in the protein.
P. Legendre, A. Navarrete, J. Rayes, C. Casari +9 more
2013Blood28 citations Open access
Semantic Scholar
Laboratory diagnosis of von Willebrand disease
A. Veyradier, É. Fressinaud, D. Meyer
1998International journal of clinical & laboratory research (Print)26 citations
Semantic Scholar
Mutational analysis of the von Willebrand factor gene in type 1 von Willebrand disease using conformation sensitive gel electrophoresis: a comparison of fluorescent and manual techniques.
Mohammad Hashemi Soteh, I. Peake, L. Marsden, J. Anson +7 more
2007Haematologica23 citations Open access
Semantic Scholar
Mutations C1157F and C1234W of von Willebrand factor cause intracellular retention with defective multimerization and secretion
A. Hommais, A. Stépanian, É. Fressinaud, C. Mazurier +3 more
2006Journal of Thrombosis and Haemostasis22 citations Open access
Semantic Scholar
Somatic mosaicism and compound heterozygosity in female hemophilia B.
Jean-marc Costa, D. Vidaud, I. Laurendeau, M. Vidaud +5 more
2000Blood20 citations Open access
Semantic Scholar

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