O. Chafa

发表

Factor VII gene intronic mutation in a lethal factor VII deficiency: effects on splice-site selection.

S. Amselem, K. Borensztajn, M. Sobrier, 2003, Blood.

Characterization of two novel splice site mutations in human factor VII gene causing severe plasma factor VII deficiency and bleeding diathesis

K. Borensztajn, M. Alhenc-Gelas, A. Fischer, 2002, British journal of haematology.

Characterization of a homozygous Gly11Val mutation in the Gla domain of coagulation factor X.

M. Tagzirt, A. Fischer, O. Chafa, 2009, Thrombosis research.

Clinical, biological, and genetic features in an afibrinogenemia patient series in Algeria

P. de Mazancourt, T. Mirault, A. Fischer, 2022, Haemophilia : the official journal of the World Federation of Hemophilia.

Severe hypofibrinogenemia associated with bilateral ischemic necrosis of toes and fingers.

A. Fischer, O. Chafa, A. Reghis, 1995, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

Homozygous nonsense mutation (Cys72→stop) in the human F7 gene: a not life‐threatening mutation despite the absence of circulating factor VII

A. Fischer, O. Chafa, J. Tapon-Bretaudière, 2005, Journal of thrombosis and haemostasis : JTH.

Prevalence of the FVQ506 (factor V Leiden) mutation in the normal and thrombophilic Algerian population.

A. Fischer, O. Chafa, A. Reghis, 1997, British journal of haematology.

Antithrombin III Alger: A New Homozygous AT III Variant

M. Desnos, S. Béguin, M. Dautzenberg, 1986, Thrombosis and Haemostasis.

Behçet Syndrome Associated with Protein S Deficiency

A. Fischer, O. Chafa, M. Benabadji, 1992, Thrombosis and Haemostasis.

A new case of ‘type II’ inherited protein S deficiency

A. Fischer, O. Chafa, M. Benabadji, 1989, British journal of haematology.

Lethal factor VII deficiency due to novel mutations in the F7 promoter: Functional analysis reveals disruption of HNF4 binding site

E. Lopez, M. Claustres, M. Taulan, 2012, Thrombosis and Haemostasis.

Inherited factor VII deficiency: identification of two novel mutations (A191V and T239P) in the catalytic domain.

K. Borensztajn, H. Wajcman, B. L. Le Bonniec, 2005, Thrombosis research.

Prevalence of the Prothrombin Gene 20210A Mutation in Thrombophilic and Healthy Algerian Subjects

A. Fischer, O. Chafa, A. Reghis, 1999, Thrombosis and Haemostasis.