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Sonia Nouioua

Showing results (1-10 of 17) with videos related to

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Revue Neurologique|May 3, 2024
Distal hereditary motor neuropathiesMeriem Tazir, Sonia Nouioua
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.
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.
Medecine Sciences : M/S|December 8, 2021
[A case of congenital limb girdle myasthenia solved through a tripartite collaboration]Sonia Nouioua, Edoardo Malfatti, Ravenscroft Gianina, et al.
Medecine Sciences : M/S|January 17, 2023
[The high phenotypic variability of RYR1 gene mutations]Mohamed Islam Kediha, Sonia Nouioua, Meriem Tazir, et al.
Journal of Neuropathology and Experimental Neurology|January 5, 2018
Nerve Biopsy Is Still Useful in Some Inherited NeuropathiesMathilde Duchesne, Stéphane Mathis, Laurence Richard, et al.
Neuromuscular Disorders : NMD|February 24, 2009
Phenotypic variability in giant axonal neuropathyMeriem Tazir, Sonia Nouioua, Laurent Magy, et al.
Medecine Sciences : M/S|November 28, 2025
[Africa miologica: terra quasi incognita?]J Andoni Urtizberea, Ghislain Nda'h-Sekou, Sonia Nouioua, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 29, 2011
Pantothenate kinase-associated neurodegeneration: clinical description of 10 patients and identification of new mutationsSalima Assami, Hamid Azzedine, Sonia Nouioua, et al.
Neuromuscular Disorders : NMD|July 12, 2011
Novel mutations in the PRX and the MTMR2 genes are responsible for unusual Charcot-Marie-Tooth disease phenotypesSonia Nouioua, Tarik Hamadouche, Benoit Funalot, et al.
Pageof 2

Showing results (1-10 of 17) with videos related to

Sort By:
Pageof 2
Revue Neurologique|May 3, 2024
Distal hereditary motor neuropathiesMeriem Tazir, Sonia Nouioua
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.
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.
Medecine Sciences : M/S|December 8, 2021
[A case of congenital limb girdle myasthenia solved through a tripartite collaboration]Sonia Nouioua, Edoardo Malfatti, Ravenscroft Gianina, et al.
Medecine Sciences : M/S|January 17, 2023
[The high phenotypic variability of RYR1 gene mutations]Mohamed Islam Kediha, Sonia Nouioua, Meriem Tazir, et al.
Journal of Neuropathology and Experimental Neurology|January 5, 2018
Nerve Biopsy Is Still Useful in Some Inherited NeuropathiesMathilde Duchesne, Stéphane Mathis, Laurence Richard, et al.
Neuromuscular Disorders : NMD|February 24, 2009
Phenotypic variability in giant axonal neuropathyMeriem Tazir, Sonia Nouioua, Laurent Magy, et al.
Medecine Sciences : M/S|November 28, 2025
[Africa miologica: terra quasi incognita?]J Andoni Urtizberea, Ghislain Nda'h-Sekou, Sonia Nouioua, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 29, 2011
Pantothenate kinase-associated neurodegeneration: clinical description of 10 patients and identification of new mutationsSalima Assami, Hamid Azzedine, Sonia Nouioua, et al.
Neuromuscular Disorders : NMD|July 12, 2011
Novel mutations in the PRX and the MTMR2 genes are responsible for unusual Charcot-Marie-Tooth disease phenotypesSonia Nouioua, Tarik Hamadouche, Benoit Funalot, et al.
Pageof 2