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Prophylactic versus on-demand treatment strategies for severe haemophilia: a comparison of costs and long-term outcome

Haemophilia : the official journal of the World Federation of Hemophilia, 2002-11, Vol.8 (6), p.745-752

2002

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Epidemiological survey of the orthopaedic status of severe haemophilia A and B patients in France

Haemophilia : the official journal of the World Federation of Hemophilia, 2000-01, Vol.6 (1), p.23-32

2000

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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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A retrospective study on chemical and radioactive synovectomy in severe haemophilia patients with recurrent haemarthrosis

Haemophilia : the official journal of the World Federation of Hemophilia, 1999-03, Vol.5 (2), p.115-123

1999

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Evaluation of the impact of information about treatment-related risks in patients receiving blood-derived or recombinant medications

Haemophilia : the official journal of the World Federation of Hemophilia, 2004-09, Vol.10 (5), p.572-581

2004

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Nonviolent (empathic) communication for health care providers

Haemophilia : the official journal of the World Federation of Hemophilia, 1998-07, Vol.4 (4), p.335-340

1998

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Embolized ischemic lesions of toes in an afibrinogenemic patient: possible relevance to in vivo circulating thrombin

Thrombosis research, 2001-05, Vol.102 (3), p.211-219

2001

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Endothelial binding sites for heparin. Specificity and role in heparin neutralization

Biochemical journal, 1986-09, Vol.238 (3), p.847-854

1986

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Magnetic field effects on viscous fingering of a ferrofluid in an anisotropic Hele--Shaw cell

Magnetohydrodynamics (New York, N.Y. 1965), 2005-12, Vol.41 (4), p.373-378

2005

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Molecular characterization of antithrombin III (ATIII) variants using polymerase chain reaction: identification of the ATIII Charleville as an Ala 384 Pro mutation

The Journal of clinical investigation, 1989-10, Vol.84 (4), p.1236-1242

1989

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Brief report: Autoantibodies against erythropoietin in a patient with pure red-cell aplasia

The New England journal of medicine, 1996-03, Vol.334 (10), p.630-633

1996

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Important role of arginine 129 in heparin-binding site of antithrombin III. Identification of a novel mutation arginine 129 to glutamine

The Journal of biological chemistry, 1990-11, Vol.265 (31), p.18997-19001

1990

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Electrochemical deposition of iron in a thin cell under an in-plane magnetic field

Magnetohydrodynamics (New York, N.Y. 1965), 2006-12, Vol.42 (4), p.403-408

2006

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De l'héparine aux héparines: vers de nouvelles perspectives thérapeutiques?

Biomedicine & pharmacotherapy, 1987, Vol.41 (4), p.171-175

1987

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Electrochemical growth of Zn and Fe arborescences under normal magnetic field

Magnetohydrodynamics (New York, N.Y. 1965), 2003-12, Vol.39 (4), p.461-468

2003

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Molecular bases of antithrombin deficiency in French families: identification of seven novel mutations in the antithrombin gene

British journal of haematology, 2000-09, Vol.110 (3), p.731-734

2000

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Effect of tamoxifen on von Willebrand factor levels

Archives of internal medicine (1960), 1997-07, Vol.157 (14), p.1613

1997

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Binding and endocytosis of heparin by human endothelial cells in culture

Biochimica et biophysica acta, 1985-05, Vol.845 (2), p.196-203

1985

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Ombres et lumières sur les anomalies de l'hémostase associées à la maladie veineuse thromboembolique

La revue de medecine interne, 1991, Vol.12 (1), p.23-24

Molho-Sabatier, P.

1991

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Ex vivo inhibition of platelet aggregation in patients with severe limb arteriopathy treated with BAY U3405, a specific TX A2 receptor antagonist

Thrombosis and haemostasis, 1994-11, Vol.72 (5), p.659

1994

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Homocysteine, 5,10-méthylénetétrahydrofolate reductase et thrombose veineuse profonde. Enquête auprès de 120 patients en médecine interne

La revue de medecine interne, 1998, Vol.19 (1), p.29-33

1998

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Homocystéinémie et thromboses veineuses

La revue de medecine interne, 1994, Vol.15, p.124s-124s

1994

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Epidemiological survey of the orthopaedic status of severe haemophilia A and B patients in France. The French Study Group. secretariat.haemophiles@cch.ap-hop-paris.fr

Haemophilia : the official journal of the World Federation of Hemophilia, 2000-01, Vol.6 (1), p.23-32

2000

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Endothélium et thrombose

La revue de medecine interne, 1987, Vol.8 (4), p.389-394

Molho-Sabatier, P.

1987

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Familial variant of antithrombin III (AT III Bligny, 47Arg to His) associated with protein C deficiency

Thrombosis and haemostasis, 1990-04, Vol.63 (2), p.215-219

1990

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Prophylactic versus on-demand treatment strategies for severe haemophilia: a comparison of costs and long-term outcome

Epidemiological survey of the orthopaedic status of severe haemophilia A and B patients in France

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

A retrospective study on chemical and radioactive synovectomy in severe haemophilia patients with recurrent haemarthrosis

Evaluation of the impact of information about treatment-related risks in patients receiving blood-derived or recombinant medications

Nonviolent (empathic) communication for health care providers

Embolized ischemic lesions of toes in an afibrinogenemic patient: possible relevance to in vivo circulating thrombin

Endothelial binding sites for heparin. Specificity and role in heparin neutralization

Magnetic field effects on viscous fingering of a ferrofluid in an anisotropic Hele--Shaw cell

Molecular characterization of antithrombin III (ATIII) variants using polymerase chain reaction: identification of the ATIII Charleville as an Ala 384 Pro mutation

Brief report: Autoantibodies against erythropoietin in a patient with pure red-cell aplasia

Important role of arginine 129 in heparin-binding site of antithrombin III. Identification of a novel mutation arginine 129 to glutamine

Electrochemical deposition of iron in a thin cell under an in-plane magnetic field

De l'héparine aux héparines: vers de nouvelles perspectives thérapeutiques?

Electrochemical growth of Zn and Fe arborescences under normal magnetic field

Molecular bases of antithrombin deficiency in French families: identification of seven novel mutations in the antithrombin gene

Effect of tamoxifen on von Willebrand factor levels

Binding and endocytosis of heparin by human endothelial cells in culture

Ombres et lumières sur les anomalies de l'hémostase associées à la maladie veineuse thromboembolique

Ex vivo inhibition of platelet aggregation in patients with severe limb arteriopathy treated with BAY U3405, a specific TX A2 receptor antagonist

Homocysteine, 5,10-méthylénetétrahydrofolate reductase et thrombose veineuse profonde. Enquête auprès de 120 patients en médecine interne

Homocystéinémie et thromboses veineuses

Epidemiological survey of the orthopaedic status of severe haemophilia A and B patients in France. The French Study Group. secretariat.haemophiles@cch.ap-hop-paris.fr

Endothélium et thrombose

Familial variant of antithrombin III (AT III Bligny, 47Arg to His) associated with protein C deficiency

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