Sonia Nouioua

Spine deformities in Charcot-Marie-Tooth 4C caused by <i>SH3TC2</i> gene mutations

Hamid Azzedine, N. Ravisé, Christophe Verny et al. · Neurology · 2006 · 106 citations

Life Sciences, Genetics, Neurology +17

Arginine:glycine amidinotransferase (AGAT) deficiency: Clinical features and long term outcomes in 16 patients diagnosed worldwide

Sylvia Stöckler‐Ipsiroglu, Delia Apatean, Roberta Battini et al. · Molecular Genetics and Metabolism · 2015 · 67 citations · Full text

Life Sciences, Molecular Genetics, Neurology +17

Ataxia with oculomotor apraxia type 2: A clinical and genetic study of 19 patients

Mériem Tazir, Lamia Alipacha, A. M’zahem et al. · Journal of the Neurological Sciences · 2009 · 63 citations

Life Sciences, Genetics, Neurology +11

Phenotypic variability in giant axonal neuropathy

Mériem Tazir, Sonia Nouioua, Laurent Magy et al. · Neuromuscular Disorders · 2009 · 60 citations

Life Sciences, Neurology, Neuroscience +13

The <i>CHRNE</i> 1293insG founder mutation is a frequent cause of congenital myasthenia in North Africa

Pascale Richard, Karen Gaudon, Asma Ammar et al. · Neurology · 2008 · 41 citations

Life Sciences, Genetics, Molecular Genetics +16