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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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Antiphospholipid Antibodies and Procoagulant Profile in Tunisians With Inflammatory Bowel Diseases
The hypercoagulable state accompanying inflammatory bowel diseases (IBDs) is still poorly understood. The aim of this study was to assess antiphospholipid antibodies (APAs) and a large panel ofExpand
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A prospective study of the prevalence of heparin‐induced antibodies and other associated thromboembolic risk factors in pediatric patients undergoing hemodialysis
Heparin, which is used at high doses in hemodialysis patients, may induce antibodies favoring thromboembolic complications. We prospectively investigated the prevalence of heparin‐inducedExpand
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[Dysfibrinogenemia and thrombosis. A case report].
BACKGROUND Congenital dysfibrinogenemia is a functional disorder of the fibrinogen that represents a rare cause of thrombophilia. AIM To report a Tunisian case of the association dysfibrinogenemiaExpand
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Platelet‐specific alloantigens and antibodies in Tunisian women after three or more pregnancies
Pregnancy may allow alloimmunization against human platelet antigens (HPA), which can lead to neonatal alloimmune thrombocytopenia (NAIT). The specificities of alloantibodies are closely related toExpand
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Antibodies to anionic phospholipids and cofactors in kala-azar. Comparative study with malaria, toxoplasmosis and "autoimmune diseases".
OBJECTIVE To investigate the distribution of various anti-anionic and anti-cofactor phospholipid antibodies in children with kala-azar, and to compare them to malaria, toxoplasmosis and auto-immuneExpand
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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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[Primary renal non-Hodgkin lymphoma].
Primary renal non Hodgkin lymphoma is rare and unusual because the renal parenchyma does not have lymphatics. We report a case of bilateral primary lymphoblastic T lymphoma presenting with renalExpand
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