Last Updated: 09/26/2026
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Found 98 publications
Advancing neurogenetics in Africa: past achievements, current developments and shaping the future.
Journal: Nature reviews. Neurology
Published: May 01, 2025
Identifying Clinical Measures Related to Falls in Ambulatory Patients with Spinal and Bulbar Muscular Atrophy.
Journal: Neurology international
Published: March 24, 2025
Evaluation of Sensory and Motor Function in Spinal and Bulbar Muscular Atrophy Using Quiet Stance and Reactive Postural Control.
Journal: Neurology international
Published: March 24, 2025
The evolution of eukaryotic linear motifs governing the function of androgen receptor from fish to Homo sapiens.
Journal: Nucleic acids research
Published: December 17, 2024
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
AP2A2 mutation and defective endocytosis in a Malian family with hereditary spastic paraplegia.
Journal: Neurobiology of disease
Published: January 13, 2024
Pentanucleotide Repeat Insertions in RAI1 Cause Benign Adult Familial Myoclonic Epilepsy Type 8.
Journal: Movement disorders : official journal of the Movement Disorder Society
Published: July 11, 2023
Patient-Reported Impact of Symptoms in Spinal and Bulbar Muscular Atrophy.
Journal: Neurology. Clinical practice
Published: May 11, 2023
Last Updated: 09/26/2026