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FEIBA in the treatment of acquired haemophilia A: Results from the prospective multicentre French 'FEIBA dans l'hémophilie A acquise' (FEIBHAC) registry

Haemophilia : the official journal of the World Federation of Hemophilia, 2015-05, Vol.21 (3), p.330-337

2015

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Post-authorization safety study of Clottafact®, a triply secured fibrinogen concentrate in congenital afibrinogenemia. A prospective observational study

Vox sanguinis, 2016-11, Vol.111 (4), p.383-390

2016

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Characterizing hospital pathways for the care of acquired hemophilia in France using comprehensive national health data

La revue de medecine interne, 2022-03, Vol.43 (3), p.139-144

2022

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Factor XI replacement for inherited factor XI deficiency in routine clinical practice: results of the HEMOLEVEN prospective 3-year postmarketing study

Haemophilia : the official journal of the World Federation of Hemophilia, 2015-07, Vol.21 (4), p.481-489

2015

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Plasma D-dimer concentration in patients with systemic sclerosis

British journal of dermatology (1951), 2008-02, Vol.158 (2), p.392-395

2008

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Outcome of acquired haemophilia in France: the prospective SACHA (Surveillance des Auto antiCorps au cours de l'Hémophilie Acquise) registry

Haemophilia : the official journal of the World Federation of Hemophilia, 2013-07, Vol.19 (4), p.564-570

2013

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Prothrombotic inherited abnormalities other than factor v leiden mutation do not play a role in venous thrombosis in inflammatory bowel disease

The American journal of gastroenterology, 2001-05, Vol.96 (5), p.1448-1454

2001

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The G79A polymorphism of protein Z gene is an independent risk factor for cerebral venous thrombosis

Journal of neurology, 2008-10, Vol.255 (10), p.1521-1525

2008

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Molecular analysis of the fibrinogen gene cluster in 16 patients with congenital afibrinogenemia : novel truncating mutations in the FGA and FGG genes

Human genetics, 2001-03, Vol.108 (3), p.237-240

2001

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Decision analysis for use of platelet aggregation test, carbon 14-serotonin release assay, and heparin-platelet factor 4 enzyme-linked immunosorbent assay for diagnosis of heparin-induced thrombocytopenia

American journal of clinical pathology, 1999-05, Vol.111 (5), p.700-706

1999

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Thrombophilia and fetal growth restriction

European journal of obstetrics & gynecology and reproductive biology, 2004-03, Vol.113 (1), p.36-40

2004

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Successful long‐term replacement therapy with FXIII concentrate (Fibrogammin® P) for severe congenital factor XIII deficiency: a prospective multicentre study

Journal of thrombosis and haemostasis, 2011-06, Vol.9 (6), p.1264-1266

2011

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Analysis of biological phenotypes from 42 patients with inherited factor VII deficiency: can biological tests predict the bleeding risk?

Haematologica (Roma), 2004-06, Vol.89 (6), p.704

2004

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The IgG autoimmune response in postpartum acquired hemophilia A targets mainly the A1a1 domain of FVIII

Journal of thrombosis and haemostasis, 2012-09, Vol.10 (9), p.1814-1822

2012

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Retrobulbar optic neuritis revealing primary anti-phospholipid antibody syndrome

Scandinavian journal of rheumatology, 2007-01, Vol.36 (2), p.156-157

2007

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Venous thromboembolism during pregnancy: a retrospective study of enoxaparin safety in 624 pregnancies

BJOG : an international journal of obstetrics and gynaecology, 2001-11, Vol.108 (11), p.1134-1140

2001

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Pharmacokinetics and pharmacodynamics of a new highly secured fibrinogen concentrate

Journal of thrombosis and haemostasis, 2008-09, Vol.6 (9), p.1494-1499

2008

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Quantification of Lupus Anticoagulants in Clinical Samples Using Anti- β2GP1 and Anti-Prothrombin Monoclonal Antibodies

Thrombosis and haemostasis, 2001, Vol.86 (8), p.584-589

2001

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Differences in specificity of heparin‐dependent antibodies developed in heparin‐induced thrombocytopenia and consequences on cross‐reactivity with danaparoid sodium

British journal of haematology, 1997-11, Vol.99 (2), p.273-280

1997

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Antiphospholipid Antibodies in the Acute Phase of Cerebral Ischaemia in Young Adults: A Descriptive Study of 139 Patients

Cerebrovascular diseases (Basel, Switzerland), 2002-01, Vol.13 (3), p.156-162

2002

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Frequency of protein Z deficiency in patients with ischaemic stroke

The Lancet (British edition), 2001-03, Vol.357 (9260), p.933-934

2001

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Activated protein C sensitivity ratio in pregnant women at delivery

British journal of haematology, 1996, Vol.92 (1), p.244-246

1996

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Acute adrenal failure secondary to bilateral infarction of the adrenal glands as the first manifestation of primary antiphospholipid antibody syndrome

Annals of the rheumatic diseases, 1997-09, Vol.56 (9), p.567-568

1997

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Evaluation of Sensitivity and Specificity of a Standardized Procedure Using Different Reagents for the Detection of Lupus Anticoagulants

Thrombosis and haemostasis, 1997, Vol.77 (2), p.336-342

1997

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The A20210 allele of the prothrombin gene is not frequently associated with the factor V Arg 506 to Gln mutation in thrombophilic families

Blood, 1997-08, Vol.90 (4), p.1711-1711

1997

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FEIBA in the treatment of acquired haemophilia A: Results from the prospective multicentre French 'FEIBA dans l'hémophilie A acquise' (FEIBHAC) registry

Post-authorization safety study of Clottafact®, a triply secured fibrinogen concentrate in congenital afibrinogenemia. A prospective observational study

Characterizing hospital pathways for the care of acquired hemophilia in France using comprehensive national health data

Factor XI replacement for inherited factor XI deficiency in routine clinical practice: results of the HEMOLEVEN prospective 3-year postmarketing study

Plasma D-dimer concentration in patients with systemic sclerosis

Outcome of acquired haemophilia in France: the prospective SACHA (Surveillance des Auto antiCorps au cours de l'Hémophilie Acquise) registry

Prothrombotic inherited abnormalities other than factor v leiden mutation do not play a role in venous thrombosis in inflammatory bowel disease

The G79A polymorphism of protein Z gene is an independent risk factor for cerebral venous thrombosis

Molecular analysis of the fibrinogen gene cluster in 16 patients with congenital afibrinogenemia : novel truncating mutations in the FGA and FGG genes

Decision analysis for use of platelet aggregation test, carbon 14-serotonin release assay, and heparin-platelet factor 4 enzyme-linked immunosorbent assay for diagnosis of heparin-induced thrombocytopenia

Thrombophilia and fetal growth restriction

Successful long‐term replacement therapy with FXIII concentrate (Fibrogammin® P) for severe congenital factor XIII deficiency: a prospective multicentre study

Analysis of biological phenotypes from 42 patients with inherited factor VII deficiency: can biological tests predict the bleeding risk?

The IgG autoimmune response in postpartum acquired hemophilia A targets mainly the A1a1 domain of FVIII

Retrobulbar optic neuritis revealing primary anti-phospholipid antibody syndrome

Venous thromboembolism during pregnancy: a retrospective study of enoxaparin safety in 624 pregnancies

Pharmacokinetics and pharmacodynamics of a new highly secured fibrinogen concentrate

Quantification of Lupus Anticoagulants in Clinical Samples Using Anti- β2GP1 and Anti-Prothrombin Monoclonal Antibodies

Differences in specificity of heparin‐dependent antibodies developed in heparin‐induced thrombocytopenia and consequences on cross‐reactivity with danaparoid sodium

Antiphospholipid Antibodies in the Acute Phase of Cerebral Ischaemia in Young Adults: A Descriptive Study of 139 Patients

Frequency of protein Z deficiency in patients with ischaemic stroke

Activated protein C sensitivity ratio in pregnant women at delivery

Acute adrenal failure secondary to bilateral infarction of the adrenal glands as the first manifestation of primary antiphospholipid antibody syndrome

Evaluation of Sensitivity and Specificity of a Standardized Procedure Using Different Reagents for the Detection of Lupus Anticoagulants

The A20210 allele of the prothrombin gene is not frequently associated with the factor V Arg 506 to Gln mutation in thrombophilic families

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