Malika Chaouch
Algiers, Algeria
Last Updated: 09/26/2026
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Found 10 publications
A recurrent homozygous LMNA missense variant p.Thr528Met causes atypical progeroid syndrome characterized by mandibuloacral dysostosis, severe muscular dystrophy, and skeletal deformities.
Journal: American journal of medical genetics. Part A
Published: December 21, 2022
Clinical, Biomarker, and Molecular Delineations and Genotype-Phenotype Correlations of Ataxia With Oculomotor Apraxia Type 1.
Journal: JAMA neurology
Published: January 23, 2018
Atypical pantothenate kinase-associated neurodegeneration: Clinical description of two brothers and a review of the literature.
Journal: Revue neurologique
Published: November 24, 2016
Refining the phenotype associated with CASC5 mutation.
Journal: Neurogenetics
Published: September 02, 2015
Familial epilepsy in Algeria: Clinical features and inheritance profiles.
Journal: Seizure
Published: May 15, 2015
Greater improvement in LRRK2 G2019S patients undergoing Subthalamic Nucleus Deep Brain Stimulation compared to non-mutation carriers.
Journal: BMC neuroscience
Published: April 22, 2015
Galanin pathogenic mutations in temporal lobe epilepsy.
Journal: Human molecular genetics
Published: December 16, 2014
Molecular and clinical study of a cohort of 110 Algerian patients with autosomal recessive ataxia.
Journal: BMC medical genetics
Published: November 15, 2014
Consanguinity and epilepsy in Oran, Algeria: A case-control study.
Journal: Epilepsy research
Published: September 15, 2014
Mutation in TTI2 reveals a role for triple T complex in human brain development.
Journal: Human mutation
Published: April 02, 2013
Showing 1-10 of 10
Last Updated: 09/26/2026