Exome sequencing links corticospinal motor neuron disease to common neurodegenerative disorders G Novarino, AG Fenstermaker, MS Zaki, M Hofree, JL Silhavy, ... science 343 (6170), 506-511, 2014 | 557 | 2014 |
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 … H Azzedine, A Bolino, T Taieb, N Birouk, M Di Duca, A Bouhouche, ... The American Journal of Human Genetics 72 (5), 1141-1153, 2003 | 328 | 2003 |
Alteration of fatty-acid-metabolizing enzymes affects mitochondrial form and function in hereditary spastic paraplegia C Tesson, M Nawara, MAM Salih, R Rossignol, MS Zaki, M Al Balwi, ... The American Journal of Human Genetics 91 (6), 1051-1064, 2012 | 214 | 2012 |
Mutation in the epsilon subunit of the cytosolic chaperonin-containing t-complex peptide-1 (Cct5) gene causes autosomal recessive mutilating sensory neuropathy with spastic … A Bouhouche, A Benomar, N Bouslam, T Chkili, M Yahyaoui Journal of medical genetics 43 (5), 441-443, 2006 | 146 | 2006 |
Non-motor symptoms of Parkinson’s disease and their impact on quality of life in a cohort of Moroccan patients H Tibar, K El Bayad, A Bouhouche, EH Ait Ben Haddou, A Benomar, ... Frontiers in neurology 9, 170, 2018 | 136 | 2018 |
Spine deformities in Charcot-Marie-Tooth 4C caused by SH3TC2 gene mutations H Azzedine, N Ravise, C Verny, A Gabreëls-Festen, M Lammens, D Grid, ... Neurology 67 (4), 602-606, 2006 | 129 | 2006 |
A locus for an axonal form of autosomal recessive Charcot-Marie-Tooth disease maps to chromosome 1q21. 2-q21. 3 A Bouhouche, A Benomar, N Birouk, A Mularoni, F Meggouh, J Tassin, ... The American Journal of Human Genetics 65 (3), 722-727, 1999 | 120 | 1999 |
Mutations in CAPN1 cause autosomal-recessive hereditary spastic paraplegia Z Gan-Or, N Bouslam, N Birouk, A Lissouba, DB Chambers, J Vérièpe, ... The American Journal of Human Genetics 98 (5), 1038-1046, 2016 | 118 | 2016 |
Autosomal-recessive forms of demyelinating Charcot-Marie-Tooth disease O Dubourg, H Azzedine, C Verny, G Durosier, N Birouk, R Gouider, ... Neuromolecular medicine 8, 75-85, 2006 | 107 | 2006 |
KIF1C mutations in two families with hereditary spastic paraparesis and cerebellar dysfunction T Dor, Y Cinnamon, L Raymond, A Shaag, N Bouslam, A Bouhouche, ... Journal of medical genetics 51 (2), 137-142, 2014 | 88 | 2014 |
Mapping of a new form of pure autosomal recessive spastic paraplegia (SPG28) N Bouslam, A Benomar, H Azzedine, A Bouhouche, M Namekawa, ... Annals of neurology 57 (4), 567-571, 2005 | 79 | 2005 |
Clinical comparison between AVED patients with 744 del A mutation and Friedreich ataxia with GAA expansion in 15 Moroccan families A Benomar, M Yahyaoui, F Meggouh, A Bouhouche, M Boutchich, ... Journal of the neurological sciences 198 (1-2), 25-29, 2002 | 73 | 2002 |
LRRK2 G2019S Mutation: Prevalence and Clinical Features in Moroccans with Parkinson’s Disease A Bouhouche, H Tibar, R Ben El Haj, K El Bayad, R Razine, S Tazrout, ... Parkinson’s disease 2017 (1), 2412486, 2017 | 57 | 2017 |
Characterization of recessive Parkinson disease in a large multicenter study S Lesage, A Lunati, M Houot, SB Romdhan, F Clot, C Tesson, G Mangone, ... Annals of neurology 88 (4), 843-850, 2020 | 56 | 2020 |
Autosomal recessive axonal Charcot–Marie–Tooth disease (ARCMT2): phenotype–genotype correlations in 13 Moroccan families A Bouhouche, N Birouk, H Azzedine, A Benomar, G Durosier, D Ente, ... Brain 130 (4), 1062-1075, 2007 | 48 | 2007 |
Autosomal recessive mutilating sensory neuropathy with spastic paraplegia maps to chromosome 5p15. 31–14.1 A Bouhouche, A Benomar, N Bouslam, R Ouazzani, T Chkili, M Yahyaoui European journal of human genetics 14 (2), 249-252, 2006 | 46 | 2006 |
A novel locus for autosomal recessive spastic ataxia on chromosome 17p N Bouslam, A Bouhouche, A Benomar, S Hanein, S Klebe, H Azzedine, ... Human genetics 121, 413-420, 2007 | 33 | 2007 |
Association of vitamin D status with multiple sclerosis in a case-control study from Morocco A Skalli, EHAB Haddou, R El Jaoudi, R Razine, GA Mpandzou, H Tibar, ... Revue neurologique 174 (3), 150-156, 2018 | 22 | 2018 |
Mutation analysis of consanguineous Moroccan patients with Parkinson’s disease combining microarray and gene panel A Bouhouche, C Tesson, W Regragui, M Rahmani, V Drouet, H Tibar, ... Frontiers in Neurology 8, 567, 2017 | 21 | 2017 |
Evidence for prehistoric origins of the G2019S mutation in the North African Berber population R Ben El Haj, A Salmi, W Regragui, A Moussa, N Bouslam, H Tibar, ... PLoS One 12 (7), e0181335, 2017 | 21 | 2017 |