Fathi Amri

Oxidant, antioxidant status and metabolic data in patients with beta-thalassemia

Asma Kassab-Chekir, Sandrine Laradi, Salima Ferchichi et al. · Clinica Chimica Acta · 2003 · 158 citations

Life Sciences, Biochemistry, Hematology +12

Correlation of SMN2, NAIP, p44, H4F5 and Occludin genes copy number with spinal muscular atrophy phenotype in Tunisian patients

Abdelbasset Amara, Labiba Adala, Ilhem Ben Charfeddine et al. · European Journal of Paediatric Neurology · 2011 · 39 citations

Life Sciences, Genetics, Molecular Genetics +11

Steroid 21-hydroxylase gene mutational spectrum in 50 Tunisian patients: Characterization of three novel polymorphisms

Ilhem Ben Charfeddine, Felix G. Riepe, Éric Clauser et al. · Gene · 2012 · 28 citations

Life Sciences, Genetics, Molecular Genetics +16

Two novel CYP11B1 mutations in congenital adrenal hyperplasia due to steroid 11β hydroxylase deficiency in a Tunisian family

Ilhem Ben Charfeddine, Felix G. Riepe, N. Kahloul et al. · General and Comparative Endocrinology · 2011 · 23 citations

Life Sciences, Endocrinology, Genetics +17