Salimata Diallo
CHU Du Point
Bamako, BKO, Mali
Bamako, BKO, Mali
Last Updated: 09/26/2026
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Found 18 publications
Rare Variants Cause Charcot-Marie-Tooth Disease in Malian Families.
Journal: Brain and behavior
Published: September 19, 2024
A Novel Splice Site Variant in COL6A1 Causes Ullrich Congenital Muscular Dystrophy in a Consanguineous Malian Family.
Journal: Molecular genetics & genomic medicine
Published: August 05, 2024
Genetic profile of progressive myoclonic epilepsy in Mali reveals novel findings.
Journal: Frontiers in neurology
Published: June 26, 2024
The burden of headache and a health-care needs assessment in the adult population of Mali: a cross-sectional population-based study.
Journal: The journal of headache and pain
Published: May 20, 2024
A novel variant in the GNE gene in a Malian patient presenting with distal myopathy.
Journal: Neurogenetics
Published: April 06, 2024
A novel variant in the GNE gene in a Malian patient presenting with distal myopathy.
Journal: Research square
Published: March 18, 2024
AP2A2 mutation and defective endocytosis in a Malian family with hereditary spastic paraplegia.
Journal: Neurobiology of disease
Published: January 13, 2024
Assessing traditional medicine in the treatment of neurological disorders in Mali: prelude to efficient collaboration.
Journal: BMC complementary medicine and therapies
Published: October 23, 2023
Clinical and Genetic Aspects of Huntington's Disease in the Malian Population.
Journal: Journal of Huntington's disease
Published: March 21, 2022
Hereditary spastic paraplegia in Mali: epidemiological and clinical features.
Journal: Acta neurologica Belgica
Published: March 11, 2022
GJB1 variants in Charcot-Marie-Tooth disease X-linked type 1 in Mali.
Journal: Journal of the peripheral nervous system : JPNS
Published: November 26, 2021
Last Updated: 09/26/2026