Ilhem Turki

AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders

Vincenzo Salpietro, Christine L. Dixon, Hui Guo et al. · Nature Communications · 2019 · 249 citations · Full text

Life Sciences, Genetics, Neuroscience +17

Effect of vitamin E supplementation in patients with ataxia with vitamin E deficiency

S. Gabsi, N. Gouider‐Khouja, Samir Belal et al. · European Journal of Neurology · 2001 · 147 citations

Medicine, Neurology, Pharmacotherapy +13

Phenotypic Features and Genetic Findings in Sacsin-Related Autosomal Recessive Ataxia in Tunisia

Ghada El Euch-Fayache, Irfan Lalani, Rim Amouri et al. · Archives of Neurology · 2003 · 107 citations

Life Sciences, Genetics, Neurology +15

Linkage to chromosome 13q11-12 of an autosomal recessive cerebellar ataxia in a Tunisian family

Najiba Fekih Mrissa, Samir Belal, C. Ben Hamida et al. · Neurology · 2000 · 80 citations

Life Sciences, Genetics, Molecular Genetics +16

Electrophysiological and nerve biopsy: comparative study in Friedreich's ataxia and Friedreich's ataxia phenotype with vitamin E deficiency

M. Zouari, Moncef Feki, Christiane Ben Hamida et al. · Neuromuscular Disorders · 1998 · 64 citations

Medicine, Neurology, Neuroscience +14