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Ahmed Bouhouche
Ahmed Bouhouche
Faculté de Médecine et de Pharmacie, Rabat
在 um5r.ac.ma 的电子邮件经过验证
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引用次数
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年份
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
5572014
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
3282003
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
2142012
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
1462006
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
1362018
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
1292006
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
1201999
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
1182016
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
1072006
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
882014
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
792005
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
732002
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
572017
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
562020
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
482007
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
462006
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
332007
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
222018
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
212017
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
212017
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