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Hémophilie A acquise. Étude d’une série rétrospective monocentrique de 39 patients

La revue de medecine interne, 2013-01, Vol.34 (1), p.4-11

2013

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Prospective evaluation of the ‘4Ts’ score and particle gel immunoassay specific to heparin/PF4 for the diagnosis of heparin‐induced thrombocytopenia

Journal of thrombosis and haemostasis, 2007-07, Vol.5 (7), p.1373-1379

2007

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Cross‐reactivity of human anti‐ FVIII antibodies to porcine rFVIII : French field study to validate the modified Nijmegen method

International journal of laboratory hematology, 2024-06

2024

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Use of a thrombopoietin receptor agonist in von Willebrand disease type 2B (p.V1316M) with severe thrombocytopenia and intracranial hemorrhage

Platelets (Edinburgh), 2017-07, Vol.28 (5), p.518-520

2017

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Diagnosis and management challenges in patients with mild haemophilia A and discrepant FVIII measurements

Haemophilia : the official journal of the World Federation of Hemophilia, 2014-07, Vol.20 (4), p.550-558

2014

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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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Confirmed validation of an innovative PCR-assay without DNA extraction for multiplex diagnosis of factor V Leiden and prothrombin gene variants

Thrombosis research, 2019-11, Vol.183, p.143-145

2019

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FranceCoag: a 22-year prospective follow-up of the national French cohort of patients with inherited bleeding disorders

European journal of epidemiology, 2019-05, Vol.34 (5), p.521-532

2019

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Prevalence, biological phenotype and genotype in moderate/mild hemophilia A with discrepancy between one‐stage and chromogenic factor VIII activity

Journal of thrombosis and haemostasis, 2011-03, Vol.9 (3), p.524-530

2011

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Discrepancies between one stage assay and chromogenic substrate assay in patients treated with recombinant or plasma-derived FVIII and usefulness of a specific standard in ReFacto AF®-treated patients

Haemophilia : the official journal of the World Federation of Hemophilia, 2016-03, Vol.22 (2), p.e101-e103

2016

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Intérêt d’explorations complémentaires devant des taux d’antithrombine limites pour authentifier un déficit responsable d’un risque thrombotique

Journal de médecine vasculaire, 2019-03, Vol.44 (2), p.147-147

2019

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Agreement between factor XIII activity and antigen assays in measurement of factor XIII: A French multicenter study of 147 human plasma samples

International Journal of Laboratory Hematology, 2017-06, Vol.39 (3), p.279-285

2017

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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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The use of the new ReFacto AF Laboratory Standard allows reliable measurement of FVIII:C levels in ReFacto AF mock plasma samples by a one-stage clotting assay

Haemophilia : the official journal of the World Federation of Hemophilia, 2011-09, Vol.17 (5), p.e958-e962

2011

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Does the presence of von Willebrand factor in FVIII-deficient plasma influences the measurement of FVIII inhibitor titres in haemophilia A patients?

International journal of laboratory hematology, 2015-02, Vol.37 (1), p.125-132

2015

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An unexpected transmission of von Willebrand disease type 3: the first case of maternal uniparental disomy 12

Haematologica (Roma), 2011-10, Vol.96 (10), p.1567-1568

2011

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Management of bleeding in severe factor V deficiency with a factor V inhibitor

Vox sanguinis, 2014-07, Vol.107 (1), p.97-99

2014

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Fibrinogen angers with a new deletion (γ GVYYQ 346‐350) causes hypofibrinogenemia with hepatic storage

Journal of thrombosis and haemostasis, 2007-10, Vol.5 (10), p.1999-2005

2007

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Évaluation qualitative des recherches d’antiphospholipides et devenir des patients suspects de SAPL au CHU de Nantes

La revue de medecine interne, 2013-12, Vol.34, p.A38-A39

2013

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Diagnostic du syndrome des antiphospholipides : étude de pertinence et d’exhaustivité des prescriptions biologiques

La revue de medecine interne, 2011-12, Vol.32, p.S283-S284

2011

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Une pathologie rare mais au risque hémorragique très élevé : l'hémophilie A acquise

Annales de biologie clinique (Paris), 2000, Vol.58 (6), p.741-744

2000

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Sténose d’allure athéromateuse au cours du syndrome des antiphospholipides chez cinq patients : caractéristiques cliniques et particularités biologiques

La revue de medecine interne, 2012-12, Vol.33, p.A29-A29

2012

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Acquired hemophilia A. A monocentric retrospective study of 39 patients

La revue de medecine interne, 2013-01, Vol.34 (1), p.4-11

2013

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Maladie de Willebrand acquise et syndromes lymphoprolifératifs

La Presse médicale (1983), 2001-02, Vol.30 (5), p.209-212

2001

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A novel panel of blood markers to assess the degree of liver fibrosis

Hepatology (Baltimore, Md.), 2005-12, Vol.42 (6), p.1373-1381

2005

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Hémophilie A acquise. Étude d’une série rétrospective monocentrique de 39 patients

Prospective evaluation of the ‘4Ts’ score and particle gel immunoassay specific to heparin/PF4 for the diagnosis of heparin‐induced thrombocytopenia

Cross‐reactivity of human anti‐ FVIII antibodies to porcine rFVIII : French field study to validate the modified Nijmegen method

Use of a thrombopoietin receptor agonist in von Willebrand disease type 2B (p.V1316M) with severe thrombocytopenia and intracranial hemorrhage

Diagnosis and management challenges in patients with mild haemophilia A and discrepant FVIII measurements

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

Confirmed validation of an innovative PCR-assay without DNA extraction for multiplex diagnosis of factor V Leiden and prothrombin gene variants

FranceCoag: a 22-year prospective follow-up of the national French cohort of patients with inherited bleeding disorders

Prevalence, biological phenotype and genotype in moderate/mild hemophilia A with discrepancy between one‐stage and chromogenic factor VIII activity

Discrepancies between one stage assay and chromogenic substrate assay in patients treated with recombinant or plasma-derived FVIII and usefulness of a specific standard in ReFacto AF®-treated patients

Intérêt d’explorations complémentaires devant des taux d’antithrombine limites pour authentifier un déficit responsable d’un risque thrombotique

Agreement between factor XIII activity and antigen assays in measurement of factor XIII: A French multicenter study of 147 human plasma samples

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

The use of the new ReFacto AF Laboratory Standard allows reliable measurement of FVIII:C levels in ReFacto AF mock plasma samples by a one-stage clotting assay

Does the presence of von Willebrand factor in FVIII-deficient plasma influences the measurement of FVIII inhibitor titres in haemophilia A patients?

An unexpected transmission of von Willebrand disease type 3: the first case of maternal uniparental disomy 12

Management of bleeding in severe factor V deficiency with a factor V inhibitor

Fibrinogen angers with a new deletion (γ GVYYQ 346‐350) causes hypofibrinogenemia with hepatic storage

Évaluation qualitative des recherches d’antiphospholipides et devenir des patients suspects de SAPL au CHU de Nantes

Diagnostic du syndrome des antiphospholipides : étude de pertinence et d’exhaustivité des prescriptions biologiques

Une pathologie rare mais au risque hémorragique très élevé : l'hémophilie A acquise

Sténose d’allure athéromateuse au cours du syndrome des antiphospholipides chez cinq patients : caractéristiques cliniques et particularités biologiques

Acquired hemophilia A. A monocentric retrospective study of 39 patients

Maladie de Willebrand acquise et syndromes lymphoprolifératifs

A novel panel of blood markers to assess the degree of liver fibrosis

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