Dina Ben Mohamed
Tunis, Tunisia
Last Updated: 09/26/2026
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Found 10 publications
LRRK2 G2019S as a shared mutation in two distinct double-mutant Parkinson's disease cases: First cases from Tunisia.
Journal: Parkinsonism & related disorders
Published: February 22, 2026
Fetal posterior cerebral artery infarction due to carotid dissection: a case report.
Journal: Journal of medical case reports
Published: June 18, 2025
A Mild Ataxia-Dominant Phenotype of Phosphomannomutase 2-Congenital Disorder of Glycosylation in a Tunisian Family: Broadening the Geographical Scope.
Journal: Journal of movement disorders
Published: April 18, 2025
Chorea associated with vitamin B12 deficiency in adults: a case report and review of literature.
Journal: Journal of neurology
Published: November 27, 2024
Genetic heterogeneity within a consanguineous family involving TTPA and SETX genes.
Journal: Journal of neurogenetics
Published: December 18, 2023
Cerebral large vessels vasculitis following Guillain-Barré syndrome as first clinical manifestations of primary Sjogren's syndrome: A case based - Review.
Journal: Heliyon
Published: December 08, 2023
Cognitive and psychiatric signs revealing Sneddon syndrome: A case report.
Journal: Clinical case reports
Published: September 05, 2022
Adult mild encephalitis with reversible splenial lesion and catatonia: A case report.
Journal: Heliyon
Published: August 15, 2021
A Tunisian patient with CLCN2-related leukoencephalopathy.
Journal: Clinical case reports
Published: April 27, 2021
Showing 1-10 of 10
Last Updated: 09/26/2026