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Meriem Tazir

Showing results (1-10 of 51) with videos related to

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Revue Neurologique|May 3, 2024
Distal hereditary motor neuropathiesMeriem Tazir, Sonia Nouioua
The International Journal of Neuroscience|December 29, 2022
The methylenetetrahydrofolate reductase C677T and A1298C genetic polymorphisms and plasma homocysteine in Alzheimer's disease in an Algerian populationKhadidja Bouguerra, Meriem Tazir, Hamid Melouli, et al.
Journal of the Peripheral Nervous System : JPNS|June 21, 2013
Autosomal recessive Charcot-Marie-Tooth disease: from genes to phenotypesMeriem Tazir, Mounia Bellatache, Sonia Nouioua, et al.
La Revue Du Praticien|January 23, 2009
[Hereditary neuropathies]Jean-Michel Vallat, Judith Calvo, Karima Ghorab, et al.
Journal of Neuropathology and Experimental Neurology|May 17, 2005
Autosomal-recessive Charcot-Marie-Tooth diseasesJean-Michel Vallat, Meriem Tazir, Corinne Magdelaine, et al.
Journal of the Neurological Sciences|December 3, 2014
Hereditary motor and sensory neuropathies or Charcot-Marie-Tooth diseases: an updateMeriem Tazir, Tarik Hamadouche, Sonia Nouioua, et al.
Journal of Medical Case Reports|March 26, 2022
Moderate phenotype of a congenital myasthenic syndrome type 19 caused by mutation of the COL13A1 gene: a case reportMohamed Islam Kediha, Meriem Tazir, Damien Sternberg, et al.
Neurology. Clinical Practice|May 13, 2024
Innovative Therapeutic Approaches in Congenital Myasthenic SyndromesMohamed I Kediha, Meriem Tazir, Damien Sternberg, et al.
Medecine Sciences : M/S|November 17, 2023
[Congenital myasthenic syndromes with kinetic abnormalities of the acetylcholine receptor]Mohamed Islam Kediha, Meriem Tazir, Damien Sternberg, et al.
Neurology|February 13, 2018
Updating the classification of inherited neuropathies: Results of an international surveyLaurent Magy, Stéphane Mathis, Gwendal Le Masson, et al.
Pageof 6

Showing results (1-10 of 51) with videos related to

Sort By:
Pageof 6
Revue Neurologique|May 3, 2024
Distal hereditary motor neuropathiesMeriem Tazir, Sonia Nouioua
The International Journal of Neuroscience|December 29, 2022
The methylenetetrahydrofolate reductase C677T and A1298C genetic polymorphisms and plasma homocysteine in Alzheimer's disease in an Algerian populationKhadidja Bouguerra, Meriem Tazir, Hamid Melouli, et al.
Journal of the Peripheral Nervous System : JPNS|June 21, 2013
Autosomal recessive Charcot-Marie-Tooth disease: from genes to phenotypesMeriem Tazir, Mounia Bellatache, Sonia Nouioua, et al.
La Revue Du Praticien|January 23, 2009
[Hereditary neuropathies]Jean-Michel Vallat, Judith Calvo, Karima Ghorab, et al.
Journal of Neuropathology and Experimental Neurology|May 17, 2005
Autosomal-recessive Charcot-Marie-Tooth diseasesJean-Michel Vallat, Meriem Tazir, Corinne Magdelaine, et al.
Journal of the Neurological Sciences|December 3, 2014
Hereditary motor and sensory neuropathies or Charcot-Marie-Tooth diseases: an updateMeriem Tazir, Tarik Hamadouche, Sonia Nouioua, et al.
Journal of Medical Case Reports|March 26, 2022
Moderate phenotype of a congenital myasthenic syndrome type 19 caused by mutation of the COL13A1 gene: a case reportMohamed Islam Kediha, Meriem Tazir, Damien Sternberg, et al.
Neurology. Clinical Practice|May 13, 2024
Innovative Therapeutic Approaches in Congenital Myasthenic SyndromesMohamed I Kediha, Meriem Tazir, Damien Sternberg, et al.
Medecine Sciences : M/S|November 17, 2023
[Congenital myasthenic syndromes with kinetic abnormalities of the acetylcholine receptor]Mohamed Islam Kediha, Meriem Tazir, Damien Sternberg, et al.
Neurology|February 13, 2018
Updating the classification of inherited neuropathies: Results of an international surveyLaurent Magy, Stéphane Mathis, Gwendal Le Masson, et al.
Pageof 6