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Publikováno v:
Transfusion Clinique et Biologique. 22:243
La securite transfusionnelle est un systeme concu dans le but d’assurer un maximum de securite a tous les acteurs intervenants dans une discipline ou le risque zero n’existe pas et qui est la transfusion sanguine. Afin d’instaurer un systeme qu
Publikováno v:
Thrombosis and Haemostasis. 67:001-003
SummaryBeçget syndrome is a multisystem disorder characterized by ocular, mucocutaneous, articular, gastrointestinal and neurologic abnormalities. We report here an unusual case of Beçget syndrome, characterized by the importance of the thrombotic
Publikováno v:
Blood coagulationfibrinolysis : an international journal in haemostasis and thrombosis. 6(6)
Severe hypofibrinogenemia was found in an Algerian woman who, since the age of 37 years, suffered three different episodes of ischemic necrosis of the toes and fingers leading to amputation of the toes and surgical removal of necrotic tissue (necreto
Publikováno v:
Thrombosis and haemostasis. 67(1)
Behçet syndrome is a multisystem disorder characterized by ocular, mucocutaneous, articular, gastrointestinal and neurologic abnormalities. We report here an unusual case of Behçet syndrome, characterized by the importance of the thrombotic events
Publikováno v:
Blood Coagulation & Fibrinolysis. 4:639-640
Publikováno v:
Fibrinolysis. 4:16
Autor:
Desnos M, O. Chafa, Anne-Marie Fischer, C. Sternberg, F. Meriane, Dautzenberg, Beguin S, P. Cornu
Publikováno v:
Thrombosis and Haemostasis. 55:218-221
SummaryA qualitative abnormality of antithrombin III (AT III) was found in the plasma of a 41-year old patient. The plasmatic AT III antigen concentration was 130% and the progressive anti-F IIa and anti-F Xa activities were normal (105% and 137%). T
Autor:
A M, Fischer, P, Cornu, C, Sternberg, F, Mériane, M D, Dautzenberg, O, Chafa, S, Beguin, M, Desnos
Publikováno v:
Thrombosis and haemostasis. 55(2)
A qualitative abnormality of antithrombin III (AT III) was found in the plasma of a 41-year old patient. The plasmatic AT III antigen concentration was 130% and the progressive anti-F IIa and anti-F Xa activities were normal (105% and 137%). The plas
Publikováno v:
British journal of haematology. 73(4)
Protein S inherited deficiency is associated with high risk of recurrent venous thrombotic disease (Broekmans et al, 1985a, b). Protein S exists as two forms in plasma, either free and functionally active or complexed with C4b-binding protein (C4b BP