Publications by authors named "M 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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Congenital myasthenic syndromes by Epsilon subunit mutations: Phenotypic profiles of 17 Algerian families.
M I Kediha, M Tazir, D Sternberg, B Eymard, L Ali Pacha

Rev Neurol (Paris)· April 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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