Mériem Tazir

University of Algiers Benyoucef Benkhedda — DZ

Neuroscience · Life Sciences

37h-index6.1kcitations135works1.82yr avg
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Research Topics

Hereditary Neurological Disorders(39), Genetic Neurodegenerative Diseases(31), Neurological diseases and metabolism(31), Mitochondrial Function and Pathology(20), Parkinson's Disease Mechanisms and Treatments(13)

Publications132 total

Biallelic <i>NDUFA9</i> variants cause a progressive neurodevelopmental disorder with prominent dystonia and mitochondrial complex I deficiency
Brain Communications·2025Open Access
<scp>NEUROMYODredger</scp> : Whole Exome Sequencing for the Diagnosis of Neurodevelopmental and Neuromuscular Disorders in Seven Countries
Clinical Genetics·2025· 2 citedOpen Access
Author response for "&lt;scp&gt;NEUROMYODredger&lt;/scp&gt;: Whole Exome Sequencing for the Diagnosis of Neurodevelopmental and Neuromuscular Disorders in Seven Countries"
2025
Disease Progression in Charcot‐Marie‐Tooth Disease Type <scp>4B</scp> (<scp>CMT4B</scp>) Associated With Mutations in Myotubularin‐Related Proteins 2 and 13
European Journal of Neurology·2025· 1 citedOpen Access
Innovative Therapeutic Approaches in Congenital Myasthenic Syndromes
Neurology Clinical Practice·2024Open Access
Distal hereditary motor neuropathies
Revue Neurologique·2024· 8 cited
Les syndromes myasthéniques congénitaux avec anomalies cinétiques du récepteur à l’acétylcholine
médecine/sciences·2023Open Access
Loss of phospholipase PLAAT3 causes a mixed lipodystrophic and neurological syndrome due to impaired PPARγ signaling
Nature Genetics·2023· 23 citedOpen Access
Disability and prognostic factors of MS severity: An Algerian cohort study
Journal of Neurological Research And Therapy·2023Open Access
Les comorbidités non psychiatriques associées à la sclérose en plaques : à propos d’une cohorte algérienne
Revue Neurologique·2023
La grande variabilité phénotypique des mutations du gène <i>RYR1</i>
médecine/sciences·2022Open Access
<i>PTPA</i> variants and impaired PP2A activity in early-onset parkinsonism with intellectual disability
Brain·2022· 28 citedOpen Access
A homozygous MED11 C-terminal variant causes a lethal neurodegenerative disease
Genetics in Medicine·2022· 17 citedOpen Access
Moderate phenotype of a congenital myasthenic syndrome type 19 caused by mutation of the COL13A1 gene: a case report
Journal of Medical Case Reports·2022· 5 citedOpen Access
Heterozygous <scp><i>EIF2AK2</i></scp> Variant Causes Adolescence‐Onset Generalized Dystonia Partially Responsive to <scp>DBS</scp>
Movement Disorders Clinical Practice·2021· 12 citedOpen Access
Moderate phenotype of a congenital myasthenic syndrome type 19 in an Algerian patient
Journal of the Neurological Sciences·2021
Familial and sporadic forms of MS in Algeria: Are there distinctive clinical and genetic features?
Journal of the Neurological Sciences·2021
Clinical management and disease-modifying treatment for amyotrophic lateral sclerosis in African hospital centers: the TROPALS study
Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration·2021· 3 cited
NTRK1 gene-related congenital insensitivity to pain with anhidrosis: a nationwide multicenter retrospective study
Neurogenetics·2021· 11 cited
Newborn screening programs for spinal muscular atrophy worldwide: Where we stand and where to go
Neuromuscular Disorders·2021· 165 cited
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Frequent Co-authors

Alexis Brice(22), Alexandra Dürr(16), Suzanne Lesage(12), Sonia Nouioua(12), Djamel Grid(10), Christine Tranchant(10), Traki Benhassine(10), Mathieu Anheim(9), Ebba Lohmann(8), Marie Vidailhet(8), Abdelmadjid Hamri(8), Cyril Goizet(8), Tarik Hamadouche(8), Pierre Pollak(7), Jean‐Christophe Corvol(7), Michel Kœnig(7), Laurent Magy(7), Jean‐Michel Vallat(7), François Tison(6), Giovanni Stévanin(6)