Naima Bouslam
Rabat, Morocco
Last Updated: 09/26/2026
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Found 19 publications
Novel WFS1 Variants in Two Moroccan Families with Wolfram Syndrome.
Journal: Genetic testing and molecular biomarkers
Published: May 09, 2024
Exercise Habits in People with Parkinson's: A Multinational Survey.
Journal: Movement disorders clinical practice
Published: December 13, 2023
Gene Panel Sequencing Analysis Revealed a Strong Contribution of Rare Coding Variants to the Risk of Parkinson's Disease in Sporadic Moroccan Patients.
Journal: Journal of molecular neuroscience : MN
Published: April 13, 2023
A Specific Diplotype H1j/H2 of the MAPT Gene Could Be Responsible for Parkinson's Disease with Dementia.
Journal: Case reports in genetics
Published: May 21, 2020
Gene Panel Sequencing Identifies Novel Pathogenic Mutations in Moroccan Patients with Familial Parkinson Disease.
Journal: Journal of molecular neuroscience : MN
Published: March 22, 2020
Novel pathogenic VPS13A mutation in Moroccan family with Choreoacanthocytosis: a case report.
Journal: BMC medical genetics
Published: October 25, 2019
Genetic Analysis of Undiagnosed Juvenile GM1-Gangliosidosis by Microarray and Exome Sequencing.
Journal: Case reports in genetics
Published: September 03, 2018
Evidence for prehistoric origins of the G2019S mutation in the North African Berber population.
Journal: PloS one
Published: January 16, 2017
LRRK2 G2019S Mutation: Prevalence and Clinical Features in Moroccans with Parkinson's Disease.
Journal: Parkinson's disease
Published: December 09, 2016
Association of vitamin D status with multiple sclerosis in a case-control study from Morocco.
Journal: Revue neurologique
Published: December 01, 2016
Mutations in CAPN1 Cause Autosomal-Recessive Hereditary Spastic Paraplegia.
Journal: American journal of human genetics
Published: June 04, 2016
Last Updated: 09/26/2026