Abdelmadjid Hamri

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

Ataxia with oculomotor apraxia type 2: clinical, biological and genotype/phenotype correlation study of a cohort of 90 patients

Mathieu Anheim, B. Monga, Marie‐Céline Fleury et al. · Brain · 2009 · 248 citations · Full text

Life Sciences, Genetics, Neurology +14

Mutations in ABHD12 Cause the Neurodegenerative Disease PHARC: An Inborn Error of Endocannabinoid Metabolism

Torunn Fiskerstrand, Dorra H’mida-Ben Brahim, Stefan Johansson et al. · The American Journal of Human Genetics · 2010 · 233 citations · Full text

Life Sciences, Genetics, Molecular Genetics +15

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

Clinical Heterogeneity of Autosomal Recessive Spastic Paraplegias

Paula Coutinho, José Barros, R. Zemmouri et al. · Archives of Neurology · 1999 · 93 citations

Life Sciences, Genetics, Neurology +17