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A quantitative analysis of bleeding symptoms in type 1 von Willebrand disease: results from a multicenter European study (MCMDM‐1 VWD)

Journal of thrombosis and haemostasis, 2006-04, Vol.4 (4), p.766-773

2006

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Mild hemophilia A with factor VIII assay discrepancy: using thrombin generation assay to assess the bleeding phenotype

Journal of thrombosis and haemostasis, 2008-03, Vol.6 (3), p.486-493

2008

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Platelet function analyser (PFA-100) results and von Willebrand factor deficiency: a 16-year 'real-world' experience

Haemophilia : the official journal of the World Federation of Hemophilia, 2015-09, Vol.21 (5), p.646-652

2015

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Validation of the first commercial ELISA for type 2N von Willebrand's disease diagnosis

Haemophilia : the official journal of the World Federation of Hemophilia, 2011-11, Vol.17 (6), p.944-951

2011

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Expression of 14 von Willebrand factor mutations identified in patients with type 1 von Willebrand disease from the MCMDM‐1VWD study

Journal of thrombosis and haemostasis, 2009-08, Vol.7 (8), p.1304-1312

2009

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Compound heterozygosity or heterozygosity with two mutations in cis on the same allele? A rebuttal to the letter to the Editors: Koessler et al. Von Willebrand disease caused by compound heterozygosity for p.R854Q and p.R760C: diagnostic and therapeutic implications. Haemophilia 2011; 17: e240-2

Haemophilia : the official journal of the World Federation of Hemophilia, 2011-09, Vol.17 (5), p.e832-e833

2011

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Use of recombinant factor VIIa in 3 patients with inherited type I Glanzmann's thrombasthenia undergoing invasive procedures

Thrombosis and haemostasis, 2000-05, Vol.83 (5), p.644-647

2000

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Platelet factor 4 complexed to heparin is the target for antibodies generated in heparin-induced thrombocytopenia

Thrombosis and haemostasis, 1992, Vol.68 (1), p.95-96

1992

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Antibodies to macromolecular platelet factor 4-heparin complexes in heparin-induced thrombocytopenia: a study of 44 cases

Thrombosis and haemostasis, 1995-01, Vol.73 (1), p.21-28

1995

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Molecular basis of severe factor XI deficiency in seven families from the west of France. Seven novel mutations, including an ancient Q88X mutation

Journal of thrombosis and haemostasis, 2004-01, Vol.2 (1), p.71-76

2004

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Presence of Autoantibodies to Interleukin-8 or Neutrophil-Activating Peptide-2 in Patients With Heparin-Associated Thrombocytopenia

Blood, 1996-07, Vol.88 (2), p.410-416

1996

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Scott Syndrome, Characterized by Impaired Transmembrane Migration of Procoagulant Phosphatidylserine and Hemorrhagic Complications, Is an Inherited Disorder

Blood, 1996-02, Vol.87 (4), p.1409-1415

1996

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French previously untreated patients with severe hemophilia A after exposure to recombinant factor VIII : incidence of inhibitor and evaluation of immune tolerance

Thrombosis and haemostasis, 1998-11, Vol.80 (5), p.779-783

1998

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First identification and expression of a type 2N von Willebrand disease mutation (E1078K) located in exon 25 of von Willebrand factor gene

Journal of thrombosis and haemostasis, 2004-12, Vol.2 (12), p.2271-2273

2004

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Mutations C1157F and C1234W of von Willebrand factor cause intracellular retention with defective multimerization and secretion

Journal of thrombosis and haemostasis, 2006-01, Vol.4 (1), p.148-157

2006

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Analyses of the FranceCoag cohort support differences in immunogenicity among one plasma-derived and two recombinant factor VIII brands in boys with severe hemophilia A

Haematologica (Roma), 2018-01, Vol.103 (1), p.179-189

2018

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A new automated method for von Willebrand factor antigen measurement using latex particles

Thrombosis and haemostasis, 1999-02, Vol.81 (2), p.320-321

1999

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Evaluation of denaturing high‐performance liquid chromatography (DHPLC) in the screening of mutations in hemophilia B patients

Journal of thrombosis and haemostasis, 2004-12, Vol.2 (12), p.2267-2269

2004

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Gene Defects in 150 Unrelated French Cases with Type 2 von Willebrand Disease: from the Patient to the Gene

Thrombosis and haemostasis, 1997, Vol.78 (1), p.451-456

1997

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Plasma and albumin‐free recombinant factor VIII: pharmacokinetics, efficacy and safety in previously treated pediatric patients

Journal of thrombosis and haemostasis, 2008-08, Vol.6 (8), p.1319-1326

2008

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Identification of a new type 2M von Willebrand disease mutation also at position 1324 of von Willebrand factor

Thrombosis and haemostasis, 2002-04, Vol.87 (4), p.635-640

2002

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Expression of two type 2N von Willebrand disease mutations identified in exon 18 of von Willebrand factor gene

British journal of haematology, 2004-10, Vol.127 (2), p.184-189

2004

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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

Blood, 2001-02, Vol.97 (4), p.952-959

2001

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Compound heterozygosity or heterozygosity with two mutations in cis on the same allele?

Haemophilia : the official journal of the World Federation of Hemophilia, 2011-09, Vol.17 (5), p.e832-e833

2011

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New variant of von Willebrand disease with defective binding to factor VIII

Blood, 1989-10, Vol.74 (5), p.1591-1599

1989

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A quantitative analysis of bleeding symptoms in type 1 von Willebrand disease: results from a multicenter European study (MCMDM‐1 VWD)

Mild hemophilia A with factor VIII assay discrepancy: using thrombin generation assay to assess the bleeding phenotype

Platelet function analyser (PFA-100) results and von Willebrand factor deficiency: a 16-year 'real-world' experience

Validation of the first commercial ELISA for type 2N von Willebrand's disease diagnosis

Expression of 14 von Willebrand factor mutations identified in patients with type 1 von Willebrand disease from the MCMDM‐1VWD study

Compound heterozygosity or heterozygosity with two mutations in cis on the same allele? A rebuttal to the letter to the Editors: Koessler et al. Von Willebrand disease caused by compound heterozygosity for p.R854Q and p.R760C: diagnostic and therapeutic implications. Haemophilia 2011; 17: e240-2

Use of recombinant factor VIIa in 3 patients with inherited type I Glanzmann's thrombasthenia undergoing invasive procedures

Platelet factor 4 complexed to heparin is the target for antibodies generated in heparin-induced thrombocytopenia

Antibodies to macromolecular platelet factor 4-heparin complexes in heparin-induced thrombocytopenia: a study of 44 cases

Molecular basis of severe factor XI deficiency in seven families from the west of France. Seven novel mutations, including an ancient Q88X mutation

Presence of Autoantibodies to Interleukin-8 or Neutrophil-Activating Peptide-2 in Patients With Heparin-Associated Thrombocytopenia

Scott Syndrome, Characterized by Impaired Transmembrane Migration of Procoagulant Phosphatidylserine and Hemorrhagic Complications, Is an Inherited Disorder

French previously untreated patients with severe hemophilia A after exposure to recombinant factor VIII : incidence of inhibitor and evaluation of immune tolerance

First identification and expression of a type 2N von Willebrand disease mutation (E1078K) located in exon 25 of von Willebrand factor gene

Mutations C1157F and C1234W of von Willebrand factor cause intracellular retention with defective multimerization and secretion

Analyses of the FranceCoag cohort support differences in immunogenicity among one plasma-derived and two recombinant factor VIII brands in boys with severe hemophilia A

A new automated method for von Willebrand factor antigen measurement using latex particles

Evaluation of denaturing high‐performance liquid chromatography (DHPLC) in the screening of mutations in hemophilia B patients

Gene Defects in 150 Unrelated French Cases with Type 2 von Willebrand Disease: from the Patient to the Gene

Plasma and albumin‐free recombinant factor VIII: pharmacokinetics, efficacy and safety in previously treated pediatric patients

Identification of a new type 2M von Willebrand disease mutation also at position 1324 of von Willebrand factor

Expression of two type 2N von Willebrand disease mutations identified in exon 18 of von Willebrand factor gene

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

Compound heterozygosity or heterozygosity with two mutations in cis on the same allele?

New variant of von Willebrand disease with defective binding to factor VIII

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