Ahmed Bouhouche

Exome Sequencing Links Corticospinal Motor Neuron Disease to Common Neurodegenerative Disorders

Gaia Novarino, Ali G. Fenstermaker, Maha S. Zaki et al. · Science · 2014 · 540 citations

Life Sciences, Genetics, Neuroscience +17

Mutations in MTMR13, a New Pseudophosphatase Homologue of MTMR2 and Sbf1, in Two Families with an Autosomal Recessive Demyelinating Form of Charcot-Marie-Tooth Disease Associated with Early-Onset Glaucoma

Hamid Azzedine, Alessandra Bolino, T. Taïeb et al. · The American Journal of Human Genetics · 2003 · 302 citations · Full text

Life Sciences, Genetics, Molecular Genetics +13

Alteration of Fatty-Acid-Metabolizing Enzymes Affects Mitochondrial Form and Function in Hereditary Spastic Paraplegia

Christelle Tesson, Magdalena Nawara, Mustafa A. Salih et al. · The American Journal of Human Genetics · 2012 · 199 citations · Full text

Life Sciences, Biochemistry, Molecular Genetics +14

Non-Motor Symptoms of Parkinson’s Disease and Their Impact on Quality of Life in a Cohort of Moroccan Patients

Houyam Tibar, Khalil El Bayad, Ahmed Bouhouche et al. · Frontiers in Neurology · 2018 · 136 citations · Full text

Medicine, Neurology, Functional Movement Assessment +16

Mutation in the epsilon subunit of the cytosolic chaperonin-containing t-complex peptide-1 (Cct5) gene causes autosomal recessive mutilating sensory neuropathy with spastic paraplegia

Ahmed Bouhouche · Journal of Medical Genetics · 2006 · 128 citations · Full text

Life Sciences, Genetics, Neurology +11