Mohamed Yahyaoui
Rabat, Morocco
Last Updated: 09/26/2026
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Found 24 publications
Genetic Analysis of Undiagnosed Juvenile GM1-Gangliosidosis by Microarray and Exome Sequencing.
Journal: Case reports in genetics
Published: September 03, 2018
Non-Motor Symptoms of Parkinson's Disease and Their Impact on Quality of Life in a Cohort of Moroccan Patients.
Journal: Frontiers in neurology
Published: October 23, 2017
Deep Brain Stimulation in Moroccan Patients With Parkinson's Disease: The Experience of Neurology Department of Rabat.
Journal: Frontiers in neurology
Published: September 30, 2017
Evidence for prehistoric origins of the G2019S mutation in the North African Berber population.
Journal: PloS one
Published: January 16, 2017
Association of vitamin D status with multiple sclerosis in a case-control study from Morocco.
Journal: Revue neurologique
Published: December 01, 2016
Stroke and syphilis: A retrospective study of 53 patients.
Journal: Revue neurologique
Published: November 10, 2016
A case of neurosyphilis presenting with essential-like tremor.
Journal: Revue neurologique
Published: October 23, 2016
Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic Paraplegia.
Journal: American journal of human genetics
Published: June 04, 2016
Clinical and genetic data of Huntington disease in Moroccan patients.
Journal: African health sciences
Published: March 10, 2016
A Novel Homozygous p.L539F Mutation Identified in PINK1 Gene in a Moroccan Patient with Parkinsonism.
Journal: BioMed research international
Published: March 02, 2016
Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic Paraplegia.
Journal: American journal of human genetics
Published: October 18, 2015
Last Updated: 09/26/2026