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Intracranial haemorrhages in French haemophilia patients (1991-2001): clinical presentation, management and prognosis factors for death

Haemophilia : the official journal of the World Federation of Hemophilia, 2005-09, Vol.11 (5), p.452-458

2005

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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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Implementation of a hepatitis A prevention policy in haemophiliacs: results from the French cohort

Haemophilia : the official journal of the World Federation of Hemophilia, 2007-11, Vol.13 (6), p.712-721

2007

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Severe factor V deficiency in two brothers with different clinical presentations

Haemophilia : the official journal of the World Federation of Hemophilia, 2012-09, Vol.18 (5), p.e383-e385

2012

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Experiences with continuous infusion of recombinant activated factor VII

Blood coagulation & fibrinolysis, 1998-03, Vol.9 Suppl 1, p.S97

1998

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A chromogenic assay allows reliable measurement of factor VIII levels in the presence of strong lupus anticoagulants

Thrombosis and haemostasis, 1998-01, Vol.79 (1), p.237-238

1998

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A cross-over pharmacokinetic study of a double viral inactivated factor IX concentrate (15 nm filtration and SD) compared to a SD factor IX concentrate

Thrombosis and haemostasis, 1998-12, Vol.80 (6), p.919-924

1998

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A three‐base deletion removing a leucine residue in a leucine‐rich repeat of platelet glycoprotein Ibα associated with a variant of Bernard‐Soulier syndrome (Nancy I)

British journal of haematology, 1995-02, Vol.89 (2), p.386-396

1995

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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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Functional mapping of anti–factor IX inhibitors developed in patients with severe hemophilia B

Blood, 2001-09, Vol.98 (5), p.1416-1423

2001

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Hemorheological and hemostatic parameters in children with nephrotic syndrome undergoing steroid therapy

Nephron (2015), 1994, Vol.68 (2), p.184-191

1994

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Déficit en facteur Willebrand et septorhinoplastie

Annales d'oto-laryngologie et de chirurgie cervico-faciale, 2007-11, Vol.124 (5), p.222-227

2007

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Role of the Leucine-Rich Domain of Platelet GPIbα in Correct Post-translational Processing – The Nancy I Bernard-Soulier Mutation Expressed on CHO Cells

Thrombosis and haemostasis, 2000, Vol.84 (7), p.104-111

2000

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Interferon alpha therapy in haemophilic patients with chronic hepatitis C: a French multicentre pilot study of 58 patients

European journal of gastroenterology & hepatology, 2001-07, Vol.13 (7), p.859-864

2001

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Infectious complications due to transfusion acquired Yersinia enterocolitica

Transfusion (Philadelphia, Pa.), 1989-05, Vol.29 (4), p.372-373

1989

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Première expérience de la perfusion continue de facteur anti-hémophilique au CHU de Nancy : description de l'organisation pluridisciplinaire et rôle du service pharmacie

Journal de pharmacie clinique, 2003-10, Vol.22 (4), p.197-204

2003

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Comparative assessment of phospholipid-binding antibodies indicates limited overlapping

Journal of clinical laboratory analysis, 1996, Vol.10 (1), p.6-12

1996

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A case of female hemophilia with a 46,XXr karyotype studied with X-chromosome DNA probes

Human genetics, 1986-02, Vol.72 (2), p.157-159

1986

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Nécroses cutanées induites par l'héparine : à propos de deux cas

Annales de biologie clinique (Paris), 2001, Vol.59 (5), p.651-654

2001

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'Eccentriplate': a new centrifugal plate for platelet concentrates

Progress in clinical and biological research, 1990, Vol.337, p.19

1990

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L'anomalie de May-Hegglin

Annales de biologie clinique (Paris), 2000, Vol.58 (2), p.204-207

2000

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Thrombopénie induite par l'héparine

Annales de cardiologie et d'angéiologie, 1999, Vol.48 (1), p.37-41

1999

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Preliminary results of a new plateletpheresis prototype based on autopheresis C

Progress in clinical and biological research, 1990, Vol.337, p.15

1990

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HLA typing in a new family with Fletcher factor deficiency

Human genetics, 1982-01, Vol.60 (1), p.71-73

1982

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Inherited factor VII deficiency and surgery: clinical data are the best criteria to predict the risk of bleeding

British journal of haematology, 2002-04, Vol.117 (1), p.172-175

2002

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Intracranial haemorrhages in French haemophilia patients (1991-2001): clinical presentation, management and prognosis factors for death

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

Implementation of a hepatitis A prevention policy in haemophiliacs: results from the French cohort

Severe factor V deficiency in two brothers with different clinical presentations

Experiences with continuous infusion of recombinant activated factor VII

A chromogenic assay allows reliable measurement of factor VIII levels in the presence of strong lupus anticoagulants

A cross-over pharmacokinetic study of a double viral inactivated factor IX concentrate (15 nm filtration and SD) compared to a SD factor IX concentrate

A three‐base deletion removing a leucine residue in a leucine‐rich repeat of platelet glycoprotein Ibα associated with a variant of Bernard‐Soulier syndrome (Nancy I)

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

Functional mapping of anti–factor IX inhibitors developed in patients with severe hemophilia B

Hemorheological and hemostatic parameters in children with nephrotic syndrome undergoing steroid therapy

Déficit en facteur Willebrand et septorhinoplastie

Role of the Leucine-Rich Domain of Platelet GPIbα in Correct Post-translational Processing – The Nancy I Bernard-Soulier Mutation Expressed on CHO Cells

Interferon alpha therapy in haemophilic patients with chronic hepatitis C: a French multicentre pilot study of 58 patients

Infectious complications due to transfusion acquired Yersinia enterocolitica

Première expérience de la perfusion continue de facteur anti-hémophilique au CHU de Nancy : description de l'organisation pluridisciplinaire et rôle du service pharmacie

Comparative assessment of phospholipid-binding antibodies indicates limited overlapping

A case of female hemophilia with a 46,XXr karyotype studied with X-chromosome DNA probes

Nécroses cutanées induites par l'héparine : à propos de deux cas

'Eccentriplate': a new centrifugal plate for platelet concentrates

L'anomalie de May-Hegglin

Thrombopénie induite par l'héparine

Preliminary results of a new plateletpheresis prototype based on autopheresis C

HLA typing in a new family with Fletcher factor deficiency

Inherited factor VII deficiency and surgery: clinical data are the best criteria to predict the risk of bleeding

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