Abdelbasset Amara

Genetics of low spinal muscular atrophy carrier frequency in sub‐Saharan Africa

Modibo Sangaré, Brant C. Hendrickson, Hammadoun Ali sango et al. · Annals of Neurology · 2014 · 40 citations · Full text

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 · 38 citations

Genetic Disorder, Medicine, Genetics +9

Cytogenetic and Molecular Aspects of Absolute Teratozoospermia: Comparison Between Polymorphic and Monomorphic Forms

Sonia Brahem, Hatem Elghezal, Houda Ghédir et al. · Urology · 2011 · 31 citations

Biology, Absolute Teratozoospermia, Cytogenetics +10

Molecular and biochemical characterization of Tunisian patients with glycogen storage disease type III

A. Mili, Ilhem Ben Charfeddine, Ons Mamaï et al. · Journal of Human Genetics · 2011 · 27 citations · Full text

Glycoproteomics, Biochemistry, Natural Sciences +11

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

Adrenal Gland, Urology, Novel Cyp11b1 Mutations +10