S. Ben Bêcher

SPRED2 loss-of-function causes a recessive Noonan syndrome-like phenotype

Marialetizia Motta, Giulia Fasano, Sina Gredy et al. · The American Journal of Human Genetics · 2021 · 80 citations · Full text

Life Sciences, Genetics, Molecular Genetics +11

Clinical and Genetic Characterization of 26 Tunisian Patients with Allgrove Syndrome

Fakhri Kallabi, Neila Belghuith, Hajer Aloulou et al. · Archives of Medical Research · 2016 · 29 citations

Life Sciences, Genetics, Molecular Genetics +6

Rare splicing defects of FAS underly severe recessive autoimmune lymphoproliferative syndrome

Nourhen Agrebi, Imen Ben‐Mustapha, N. Matoussi et al. · Clinical Immunology · 2017 · 26 citations

Life Sciences, Genetics, Molecular Genetics +12

Implementation of effective transition from pediatric to adult diabetes care: epidemiological and clinical characteristics—a pioneering experience in North Africa

L. Essaddam, Wafa Kallali, Manel Jemel et al. · Acta Diabetologica · 2018 · 18 citations

Medicine, Health Sciences, Pediatrics +17

Childhood diabetic neuropathy: a clinical and electrophysiological study.

F el Bahri-Ben Mrad, Riadh Gouider, Mohamed Fredj et al. · PubMed · 2000 · 16 citations

Medicine, Neurology, Pediatrics +17