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[Acquired amegakaryocytic thrombocytopenic purpura treated with intravenous immunoglobulins].
Acquired amegakaryocytic thrombocytopenic purpura is a rare disorder characterized by severe thrombocytopenia due to the absence of bone marrow megakaryocytes. The pathogenic mechanisms of thisExpand
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Platelet and granulocyte alloimmunisation in multitransfused Tunisian patients
Abstract:  We determined the frequency of post‐transfusion alloimmunisation against platelet and granulocyte antigens in 51 Tunisian polytransfused patients with haematological diseases. SerumExpand
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[Partial splenectomy in thalassemia major. Apropos of 19 cases].
Nineteen cases of B Thalassemia have benefited from partial splenectomy at the General Surgery Service of Farhat Hached Hospital in Sousse (Tunisia). The partial splenectomy indication was to reduceExpand
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First study of immunoglobulin and T cell receptor gene rearrangements in chronic and acute lymphoblastic leukemias from Tunisia.
We report the first characterization at the immunological and molecular level of 12 cases of chronic lymphocytic leukemia (CLL) and acute lymphoblastic leukemia (ALL) from Tunisia. Our results showExpand
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[Screening of hemoglobinopathies and molecular analysis of beta-thalassemia in Central Tunisia].
BACKGROUND Previous investigations have permitted to locate 16 beta-thalassemic mutations in different samples of the Tunisian population. One of them (IVS I nt 2: T--G) had been found only in theExpand
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Contribution of Flow Cytometry to Acute Leukemia Classification in Tunisia
The precision of immunological characterization of leukemias was improved by a certain number of technical innovations, particularly hybridoma production and standardization, resulting in monoclonalExpand
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Kala-azar méditerranéen de l'adulte : à propos de quatre observations tunisiennes
Resume En Tunisie, le kala-azar sevit dans le nord et le centre du pays, selon un mode sporadique et affecte essentiellement l'enfant. Nous rapportons les 4 premieres observations de kala-azar adulteExpand
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Maladie de Hodgkin associée à un sarcome de Kaposi et à une tuberculose des organes hématopoïétiques
L'association d'une maladie de Kaposi a une maladie de Hodgkin est rarement signalee. Nous rapportons l'observation d'une patiente agee de 57 ans, traitee pour maladie de Hodgkin et qui developpeExpand
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Frequency of specific coagulation inhibitors and antiphospholipid antibodies in Tunisian haemophiliacs.
Production of factor VIII or factor IX inhibitors is a major complication limiting the efficiency of substitutive therapy in haemophiliacs. Moreover, viral infections, the second serious complicationExpand
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Aspects épidemiologiques, cliniques et thérapeutiques de la leucémie lymphoïde chronique: A propos de 120 cas
Nous avons etudie de maniere retrospective 120 cas de leucemie lymphoide chronique diagnostiques entre le ler janvier 1988 et le 31 decembre 1998. L'âge moyen de nos patients etait de 66 ans, 75%Expand
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