Publications by authors named "Meriem Tazir"

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Loss of ANK3 Function Causes a Recessive Neurodevelopmental Disorder with Cerebellar Ataxia.
Reza Maroofian, Giulia Spoto, Dalila Moualek, Maha S Zaki, Asthik Biswas, Meriem Tazir

Mov Disord· November 2025

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Biallelic variants cause a progressive neurodevelopmental disorder with prominent dystonia and mitochondrial complex I deficiency.
Francesca Magrinelli, Lucie S Taylor, Sahar Sedighzadeh, Dalila Moualek, Mariasavina Severino, Meriem Tazir

Brain Commun· October 2025

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Disease Progression in Charcot-Marie-Tooth Disease Type 4B (CMT4B) Associated With Mutations in Myotubularin-Related Proteins 2 and 13.
Alessandro Bertini, Mary M Reilly, Chiara Pisciotta, Stefano C Previtali, Yesim Parman, Meriem Tazir

Eur J Neurol· February 2025

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NEUROMYODredger: Whole Exome Sequencing for the Diagnosis of Neurodevelopmental and Neuromuscular Disorders in Seven Countries.
Edoardo Malfatti, Alexandru Caramizaru, Hane Lee, JiHye Kim, Hussein Shoaito, Meriem Tazir

Clin Genet· February 2025

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Distal hereditary motor neuropathies.
Meriem Tazir, Sonia Nouioua

Rev Neurol (Paris)· December 2024

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The methylenetetrahydrofolate reductase C677T and A1298C genetic polymorphisms and plasma homocysteine in Alzheimer's disease in an Algerian population.
Khadidja Bouguerra, Meriem Tazir, Hamid Melouli, Malika Khelil

Int J Neurosci· August 2024

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Innovative Therapeutic Approaches in Congenital Myasthenic Syndromes.
Mohamed I Kediha, Meriem Tazir, Damien Sternberg, Bruno Eymard, Lamia Ali Pacha

Neurol Clin Pract· June 2024

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Loss of phospholipase PLAAT3 causes a mixed lipodystrophic and neurological syndrome due to impaired PPARγ signaling.
Nika Schuermans, Salima El Chehadeh, Dimitri Hemelsoet, Jérémie Gautheron, Marie-Christine Vantyghem, Meriem Tazir

Nat Genet· November 2023

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[Congenital myasthenic syndromes with kinetic abnormalities of the acetylcholine receptor].
Mohamed Islam Kediha, Meriem Tazir, Damien Sternberg, Bruno Eymard, Lamia Ali Pacha

Med Sci (Paris)· November 2023

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[The high phenotypic variability of RYR1 gene mutations].
Mohamed Islam Kediha, Sonia Nouioua, Meriem Tazir, Damien Sternberg, Joël Lunardi

Med Sci (Paris)· December 2022

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Clinical management and disease-modifying treatment for amyotrophic lateral sclerosis in African hospital centers: the TROPALS study.
Jaime Luna, Jeremy Jost, Mouhamadou Diagana, Leila Ait Aissa, Meriem Tazir

Amyotroph Lateral Scler Frontotemporal Degener· May 2022

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Moderate phenotype of a congenital myasthenic syndrome type 19 caused by mutation of the COL13A1 gene: a case report.
Mohamed Islam Kediha, Meriem Tazir, Damien Sternberg, Bruno Eymard, Lamia Alipacha

J Med Case Rep· March 2022

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Heterozygous Variant Causes Adolescence-Onset Generalized Dystonia Partially Responsive to DBS.
Francesca Magrinelli, Dalila Moualek, Meriem Tazir, Lamia Ali Pacha, Alice Verghese

Mov Disord Clin Pract· February 2022

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[A case of congenital limb girdle myasthenia solved through a tripartite collaboration].
Sonia Nouioua, Edoardo Malfatti, Ravenscroft Gianina, Sihem Hellal, Tazir Meriem

Med Sci (Paris)· November 2021

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NTRK1 gene-related congenital insensitivity to pain with anhidrosis: a nationwide multicenter retrospective study.
Andoni Echaniz-Laguna, Cecilia Altuzarra, Alain Verloes, Marta Gomez Garcia De La Banda, Susana Quijano-Roy, Meriem Tazir

Neurogenetics· October 2021

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Increasing involvement of CAPN1 variants in spastic ataxias and phenotype-genotype correlations.
Jean-Loup Méreaux, Cristina Firanescu, Giulia Coarelli, Malin Kvarnung, Rita Rodrigues, Meriem Tazir

Neurogenetics· March 2021

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Nonsteroidal Anti-inflammatory Use and LRRK2 Parkinson's Disease Penetrance.
Marta San Luciano, Caroline M Tanner, Cheryl Meng, Connie Marras, Samuel M Goldman, Meriem Tazir

Mov Disord· October 2020

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Characterization of Recessive Parkinson Disease in a Large Multicenter Study.
Suzanne Lesage, Ariane Lunati, Marion Houot, Sawssan Ben Romdhan, Fabienne Clot, Meriem Tazir

Ann Neurol· October 2020

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A multicenter retrospective study of charcot-marie-tooth disease type 4B (CMT4B) associated with mutations in myotubularin-related proteins (MTMRs).
Davide Pareyson, Tanya Stojkovic, Mary M Reilly, Sarah Leonard-Louis, Matilde Laurà, Meriem Tazir

Ann Neurol· July 2019

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Clinical features and prognosis of amyotrophic lateral sclerosis in Africa: the TROPALS study.
Jaime Luna, Mouhamadou Diagana, Leila Ait Aissa, Meriem Tazir, Lamia Ali Pacha

J Neurol Neurosurg Psychiatry· January 2019

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The classification of Charcot-Marie-Tooth diseases, a never-ending story: CMT4?
Jean-Michel Vallat, Meriem Tazir, Laurent Magy, Gwendal Le Masson, Stéphane Mathis

Brain· September 2018

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Some new proposals for the classification of inherited myopathies.
Stéphane Mathis, Meriem Tazir, Guilhem Solé, Laurent Magy, Gwendal Le Masson

J Neurol Sci· August 2018

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Clinical, Biomarker, and Molecular Delineations and Genotype-Phenotype Correlations of Ataxia With Oculomotor Apraxia Type 1.
Mathilde Renaud, Maria-Céu Moreira, Bondo Ben Monga, Diana Rodriguez, Rabab Debs, Meriem Tazir

JAMA Neurol· April 2018

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Updating the classification of inherited neuropathies: Results of an international survey.
Laurent Magy, Stéphane Mathis, Gwendal Le Masson, Cyril Goizet, Meriem Tazir

Neurology· March 2018

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Nerve Biopsy Is Still Useful in Some Inherited Neuropathies.
Mathilde Duchesne, Stéphane Mathis, Laurence Richard, Corinne Magdelaine, Philippe Corcia, Meriem Tazir

J Neuropathol Exp Neurol· February 2018

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