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M Tazir

Showing results (11-20 of 32) with videos related to

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Revue Neurologique|June 1, 2016
Classifications of neurogenetic diseases: An increasingly complex problemJ-M Vallat, C Goizet, M Tazir, et al.
Pathologie-Biologie|July 1, 2008
Prevalence and characterization of extended-spectrum beta-lactamases in Klebsiella pneumoniae in Algiers hospitals (Algeria)Y Messai, H Iabadene, T Benhassine, et al.
Revue Neurologique|February 10, 2023
Congenital myasthenic syndrome by mutation of the ColQ gene: Phenotypic and evolutionary profile of three Algerian familiesM I Kediha, M Tazir, C Magnouche, et al.
Neuromuscular Disorders : NMD|June 18, 2013
Creatine deficiency syndrome. A treatable myopathy due to arginine-glycine amidinotransferase (AGAT) deficiencyS Nouioua, D Cheillan, S Zaouidi, et al.
Clinical Microbiology and Infection : the Official Publication of the European Society of Clinical Microbiology and Infectious Diseases|June 4, 2010
High prevalence of methicillin-resistant Staphylococcus aureus clone ST80-IV in hospital and community settings in AlgiersK Antri, N Rouzic, O Dauwalder, et al.
Neuromuscular Disorders : NMD|October 26, 2002
Genetic heterogeneity in giant axonal neuropathy: an Algerian family not linked to chromosome 16q24.1M Tazir, J M Vallat, P Bomont, et al.
Human Mutation|March 26, 2003
Identification of seven novel mutations in the GAN geneP Bomont, C Ioos, C Yalcinkaya, et al.
Brain : a Journal of Neurology|June 1, 1987
Hereditary sensory neuropathy with neurotrophic keratitis. Description of an autosomal recessive disorder with a selective reduction of small myelinated nerve fibres and a discussion of the classification of the hereditary sensory neuropathiesM Donaghy, R N Hakin, J M Bamford, et al.
Brain : a Journal of Neurology|November 11, 2003
Phenotypic variability in autosomal recessive axonal Charcot-Marie-Tooth disease due to the R298C mutation in lamin A/CM Tazir, H Azzedine, S Assami, et al.
Neuromuscular Disorders : NMD|October 29, 2000
Charcot-Marie-Tooth 2-like presentation of an Algerian family with giant axonal neuropathyR Zemmouri, H Azzedine, S Assami, et al.
Pageof 4

Showing results (11-20 of 32) with videos related to

Sort By:
Pageof 4
Revue Neurologique|June 1, 2016
Classifications of neurogenetic diseases: An increasingly complex problemJ-M Vallat, C Goizet, M Tazir, et al.
Pathologie-Biologie|July 1, 2008
Prevalence and characterization of extended-spectrum beta-lactamases in Klebsiella pneumoniae in Algiers hospitals (Algeria)Y Messai, H Iabadene, T Benhassine, et al.
Revue Neurologique|February 10, 2023
Congenital myasthenic syndrome by mutation of the ColQ gene: Phenotypic and evolutionary profile of three Algerian familiesM I Kediha, M Tazir, C Magnouche, et al.
Neuromuscular Disorders : NMD|June 18, 2013
Creatine deficiency syndrome. A treatable myopathy due to arginine-glycine amidinotransferase (AGAT) deficiencyS Nouioua, D Cheillan, S Zaouidi, et al.
Clinical Microbiology and Infection : the Official Publication of the European Society of Clinical Microbiology and Infectious Diseases|June 4, 2010
High prevalence of methicillin-resistant Staphylococcus aureus clone ST80-IV in hospital and community settings in AlgiersK Antri, N Rouzic, O Dauwalder, et al.
Neuromuscular Disorders : NMD|October 26, 2002
Genetic heterogeneity in giant axonal neuropathy: an Algerian family not linked to chromosome 16q24.1M Tazir, J M Vallat, P Bomont, et al.
Human Mutation|March 26, 2003
Identification of seven novel mutations in the GAN geneP Bomont, C Ioos, C Yalcinkaya, et al.
Brain : a Journal of Neurology|June 1, 1987
Hereditary sensory neuropathy with neurotrophic keratitis. Description of an autosomal recessive disorder with a selective reduction of small myelinated nerve fibres and a discussion of the classification of the hereditary sensory neuropathiesM Donaghy, R N Hakin, J M Bamford, et al.
Brain : a Journal of Neurology|November 11, 2003
Phenotypic variability in autosomal recessive axonal Charcot-Marie-Tooth disease due to the R298C mutation in lamin A/CM Tazir, H Azzedine, S Assami, et al.
Neuromuscular Disorders : NMD|October 29, 2000
Charcot-Marie-Tooth 2-like presentation of an Algerian family with giant axonal neuropathyR Zemmouri, H Azzedine, S Assami, et al.
Pageof 4