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 · 253 citations

Life Sciences, Genetics, Neurology +17

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

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 · 181 citations · Full text

Medicine, Neurology, Neuroscience +12

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

Cyril Goizet, A. Boukhris, A. Dürr et al. · Brain · 2009 · 113 citations

Life Sciences, Genetics, Neurology +14

Spastic paraplegia due to SPAST mutations is modified by the underlying mutation and sex

Livia Parodi, Silvia Fenu, Mathieu Barbier et al. · Brain · 2018 · 111 citations · Full text

Life Sciences, Genetics, Neurology +17