Imed Feki

Mutations in SPG11 are frequent in autosomal recessive spastic paraplegia with thin corpus callosum, cognitive decline and lower motor neuron degeneration

Giovanni Stévanin, Hamid Azzedine, Paola S. Denora et al. · Brain · 2007 · 246 citations

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 · 211 citations · Full text

Including Kjellin Syndrome, Genetics, Spg15 Gene +4

Alteration of Ganglioside Biosynthesis Responsible for Complex Hereditary Spastic Paraplegia

Amir Boukhris, Rebecca Schüle, José Leal Loureiro et al. · The American Journal of Human Genetics · 2013 · 178 citations · Full text

Medicine, Physiology, Ganglioside Biosynthesis Responsible +7

CYP7B1 mutations in pure and complex forms of hereditary spastic paraplegia type 5

Cyril Goizet, A. Boukhris, A. Dürr et al. · Brain · 2009 · 109 citations

A New Locus for Autosomal Dominant Pure Spastic Paraplegia, on Chromosome 2q24-q34

Bertrand Fontaine, Claire-Sophie Davoine, Alexandra Dürr et al. · The American Journal of Human Genetics · 2000 · 97 citations · Full text

Mendelian Disorder, Genetic Disorder, Medicine +5