D. Hmida

A new form of childhood onset, autosomal recessive spinocerebellar ataxia and epilepsy is localized at 16q21-q23

Moez Gribaa, Mustafa A. Salih, Mathieu Anheim et al. · Brain · 2007 · 50 citations · Full text

Life Sciences, Genetics, Neurology +17

Placental Mesenchymal Dysplasia with Beckwith–Wiedemann Syndrome Fetus in the Context of Biparental and Androgenic Cell Lines

D. Hmida, Moez Gribaa, Tahar Yacoubi et al. · Placenta · 2008 · 45 citations

Medicine, Developmental Biology, Pathology +13

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

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

Life Sciences, Biochemistry, Molecular Biology +13

Phenotypic intrafamilial variability including H syndrome and Rosai–Dorfman disease associated with the same c.1088G > A mutation in the SLC29A3 gene

Hamza Chouk, M. Ben Rejeb, L. Boussofara et al. · Human Genomics · 2021 · 17 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16