Nizar Elleuch

Mutations in SPG11, encoding spatacsin, are a major cause of spastic paraplegia with thin corpus callosum

Giovanni Stévanin, Filippo M. Santorelli, Hamid Azzedine et al. · Nature Genetics · 2007 · 332 citations

Medicine, Neurology, Neuroscience +8

Identification of the SPG15 Gene, Encoding Spastizin, as a Frequent Cause of Complicated Autosomal-Recessive Spastic Paraplegia, Including Kjellin Syndrome

Sylvain Hanein, Elodie Martin, Amir Boukhris et al. · The American Journal of Human Genetics · 2008 · 213 citations · Full text

Life Sciences, Genetics, Molecular Genetics +8

Hereditary Spastic Paraplegia With Mental Impairment and Thin Corpus Callosum in Tunisia

Amir Boukhris, Giovanni Stévanin, Imed Feki et al. · Archives of Neurology · 2008 · 57 citations · Full text

Life Sciences, Genetics, Neurology +13

A new locus (SPG46) maps to 9p21.2-q21.12 in a Tunisian family with a complicated autosomal recessive hereditary spastic paraplegia with mental impairment and thin corpus callosum

Amir Boukhris, Imed Feki, Nizar Elleuch et al. · Neurogenetics · 2010 · 50 citations

Life Sciences, Genetics, Molecular Genetics +9

Hereditary Spastic Paraplegia With Thin Corpus Callosum

Alexander Lossos, Giovanni Stévanin, Vardiella Meiner et al. · Archives of Neurology · 2006 · 38 citations

Life Sciences, Genetics, Neurology +8