Meriem Tazir

Algiers, Algeria

Last Updated: 09/26/2026

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Found 47 publications

Loss of ANK3 Function Causes a Recessive Neurodevelopmental Disorder with Cerebellar Ataxia.

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.

Biallelic NDUFA9 variants cause a progressive neurodevelopmental disorder with prominent dystonia and mitochondrial complex I deficiency.

Journal: Brain communications

Published: January 28, 2025

NEUROMYODredger: Whole Exome Sequencing for the Diagnosis of Neurodevelopmental and Neuromuscular Disorders in Seven Countries.

NEUROMYODredger: Whole Exome Sequencing for the Diagnosis of Neurodevelopmental and Neuromuscular Disorders in Seven Countries.

Journal: Clinical genetics

Published: December 26, 2024

Disease Progression in Charcot-Marie-Tooth Disease Type 4B (CMT4B) Associated With Mutations in Myotubularin-Related Proteins 2 and 13.

Disease Progression in Charcot-Marie-Tooth Disease Type 4B (CMT4B) Associated With Mutations in Myotubularin-Related Proteins 2 and 13.

Journal: European journal of neurology

Published: October 28, 2024

Congenital myasthenic syndromes with kinetic abnormalities of the acetylcholine receptor

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.

Innovative Therapeutic Approaches in Congenital Myasthenic Syndromes.

Journal: Neurology. Clinical practice

Published: April 12, 2023

The high phenotypic variability of RYR1 gene mutations

The high phenotypic variability of RYR1 gene mutations

Journal: Medecine sciences : M/S

Published: January 17, 2023

The methylenetetrahydrofolate reductase C677T and A1298C genetic polymorphisms and plasma homocysteine in Alzheimer's disease in an Algerian population.

The methylenetetrahydrofolate reductase C677T and A1298C genetic polymorphisms and plasma homocysteine in Alzheimer's disease in an Algerian population.

Journal: The International journal of neuroscience

Published: December 29, 2022

Loss of phospholipase PLAAT3 causes a mixed lipodystrophic and neurological syndrome due to impaired PPARγ signaling.

Loss of phospholipase PLAAT3 causes a mixed lipodystrophic and neurological syndrome due to impaired PPARγ signaling.

Journal: Nature genetics

Published: December 22, 2022

Congenital myasthenic syndromes by Epsilon subunit mutations: Phenotypic profiles of 17 Algerian families.

Congenital myasthenic syndromes by Epsilon subunit mutations: Phenotypic profiles of 17 Algerian families.

Journal: Revue neurologique

Published: October 08, 2022

Distal hereditary motor neuropathies.

Distal hereditary motor neuropathies.

Journal: Revue neurologique

Published: August 02, 2022

Congenital myasthenic syndrome by mutation of the ColQ gene: Phenotypic and evolutionary profile of three Algerian families.

Congenital myasthenic syndrome by mutation of the ColQ gene: Phenotypic and evolutionary profile of three Algerian families.

Journal: Revue neurologique

Published: June 30, 2022

Showing 1-12 of 47

Last Updated: 09/26/2026