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Wijdene Elborgi

Tunis El Manar University

5

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8

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[Contribution and limits of CD157 in the detection of the paroxysmal nocturnal hemoglobinuria clone: a case report].

2021 Annales De Biologie Clinique
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Homozygous Mutation on the β-Globin Polyadenylation Signal in a Tunisian Patient with β-Thalassemia Intermedia and Coinheritance of Gilbert’s Syndrome

2017 Hemoglobin
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C0219 Inherited factor XI deficiency: A report of 11 cases and review of literature

2012 Thrombosis Research
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C0220 Incidence of hemophilia in the North of Tunisia

2012 Thrombosis Research
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[Iron overload in sickle cell anemia : a study of 94 patients].

2011 La Tunisie médicale
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