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European Journal of Human Genetics : EJHG|December 8, 2005
Autosomal recessive mutilating sensory neuropathy with spastic paraplegia maps to chromosome 5p15.31-14.1Ahmed Bouhouche, Ali Benomar, Naima Bouslam, et al.Case Reports in Genetics|December 21, 2020
A Specific Diplotype H1j/H2 of the MAPT Gene Could Be Responsible for Parkinson's Disease with DementiaImane Smaili, Imane Hajjaj, Rachid Razine, et al.Biomed Research International|July 15, 2016
A Novel Homozygous p.L539F Mutation Identified in PINK1 Gene in a Moroccan Patient with ParkinsonismRafiqua Ben El Haj, Wafaa Regragui, Rachid Tazi-Ahnini, et al.Indian Journal of Pediatrics|November 27, 2012
CLN6 p.I154del mutation causing late infantile neuronal ceroid lipofuscinosis in a large consanguineous Moroccan familyAhmed Bouhouche, Wafae Regragui, Elmostafa El Fahime, et al.Case Reports in Genetics|December 25, 2018
Genetic Analysis of Undiagnosed Juvenile GM1-Gangliosidosis by Microarray and Exome SequencingAhmed Bouhouche, Houyam Tibar, Yamna Kriouale, et al.Journal of Neurology|March 3, 2006
A new phenotype linked to SPG27 and refinement of the critical region on chromosomePascale Ribai, Giovanni Stevanin, Naima Bouslam, et al.Journal of Molecular Neuroscience : MN|June 20, 2020
Gene Panel Sequencing Identifies Novel Pathogenic Mutations in Moroccan Patients with Familial Parkinson DiseaseImane Smaili, Christelle Tesson, Wafa Regragui, et al.Annals of Neurology|January 6, 2004
Spinocerebellar ataxia with sensory neuropathy (SCA25) maps to chromosome 2pGiovanni Stevanin, Naima Bouslam, Stéphane Thobois, et al.Plos One|July 21, 2017
Evidence for prehistoric origins of the G2019S mutation in the North African Berber populationRafiqua Ben El Haj, Ayyoub Salmi, Wafa Regragui, et al.Journal of Molecular Neuroscience : MN|May 31, 2023
Gene Panel Sequencing Analysis Revealed a Strong Contribution of Rare Coding Variants to the Risk of Parkinson's Disease in Sporadic Moroccan PatientsImane Smaili, Houyam Tibar, Mounia Rahmani, et al.Pageof 4