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  1. Determination of glucose-6-phosphate dehydrogenase cut-off values in a Tunisian population
  2. Capillarys 2 Flex Piercing: Analytical performance assessment according to CLSI protocols for HbA1c quantification
  3. Setup of a Protocol of Molecular Diagnosis of β-Thalassemia Mutations in Tunisia using Denaturing High-Performance Liquid Chromatography (DHPLC)
  4. Red cell indices: differentiation between β-thalassemia trait and iron deficiency anemia and application to sickle-cell disease and sickle-cell thalassemia
  5. Detection of a novel splicing mutation causing analbuminemia in a Libyan family
  6. δ0-Thalassemia in cis of βKnossos globin gene: first homozygous description in thalassemia intermedia Libyans and first combination with codon 39 (C→T) in thalassemia intermedia Tunisian patients