Lamia Ali Pacha
Algiers, Algeria
Last Updated: 09/26/2026
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Found 11 publications
Loss of ANK3 Function Causes a Recessive Neurodevelopmental Disorder with Cerebellar Ataxia.
Journal: Movement disorders : official journal of the Movement Disorder Society
Published: May 24, 2025
Biallelic NDUFA9 variants cause a progressive neurodevelopmental disorder with prominent dystonia and mitochondrial complex I deficiency.
Journal: Brain communications
Published: January 28, 2025
Congenital myasthenic syndromes with kinetic abnormalities of the acetylcholine receptor
Journal: Medecine sciences : M/S
Published: November 17, 2023
Innovative Therapeutic Approaches in Congenital Myasthenic Syndromes.
Journal: Neurology. Clinical practice
Published: April 12, 2023
The high phenotypic variability of RYR1 gene mutations
Journal: Medecine sciences : M/S
Published: January 17, 2023
Congenital myasthenic syndromes by Epsilon subunit mutations: Phenotypic profiles of 17 Algerian families.
Journal: Revue neurologique
Published: October 08, 2022
Clinical management and disease-modifying treatment for amyotrophic lateral sclerosis in African hospital centers: the TROPALS study.
Journal: Amyotrophic lateral sclerosis & frontotemporal degeneration
Published: August 30, 2021
In-vitro immunomodulatory effects of nicotine on Nitric Oxide, interleukin 1β and interleukin 37 production in human peripheral blood mononuclear cells (PBMC) from patients with Behçet disease.
Journal: International immunopharmacology
Published: May 26, 2021
Clinical features and prognosis of amyotrophic lateral sclerosis in Africa: the TROPALS study.
Journal: Journal of neurology, neurosurgery, and psychiatry
Published: March 21, 2018
Molecular and clinical study of a cohort of 110 Algerian patients with autosomal recessive ataxia.
Journal: BMC medical genetics
Published: November 15, 2014
Showing 1-11 of 11
Last Updated: 09/26/2026