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R Amouri

Showing results (11-20 of 23) with videos related to

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Neuromuscular Disorders : NMD|June 6, 2000
A new locus for autosomal recessive limb-girdle muscular dystrophy in a large consanguineous Tunisian family maps to chromosome 19q13.3A Driss, R Amouri, C Ben Hamida, et al.
Neurology|April 6, 2000
Linkage to chromosome 13q11-12 of an autosomal recessive cerebellar ataxia in a Tunisian familyN Mrissa, S Belal, C B Hamida, et al.
La Revue De Medecine Interne|April 27, 2010
[Axonal neuropathy revealing pleural lymphoma as a long-term outcome of therapeutic pneumothorax]N Fajraoui, K Ben Hamida, A Hadj Kacem, et al.
Neurology|September 15, 2004
Aprataxin gene mutations in Tunisian familiesR Amouri, M-C Moreira, M Zouari, et al.
Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie|April 1, 1996
[Gliotoxic factor and multiple sclerosis]F Rieger, R Amouri, N Benjelloun, et al.
European Journal of Neurology|October 10, 2012
Exome sequencing: an efficient diagnostic tool for complex neurodegenerative disordersM B Hammer, G Eleuch-Fayache, J R Gibbs, et al.
Neurology|April 23, 2003
Fukutin-related protein gene mutated in the original kindred limb-girdle MD 2IA Driss, S Noguchi, R Amouri, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|May 31, 2001
Regenerative capacity of human satellite cells: the mitotic clock in cell transplantationS Di Donna, V Renault, C Forestier, et al.
Journal of the Neurological Sciences|April 30, 1998
A gliotoxic factor and multiple sclerosisA Ménard, R Amouri, T Dobránsky, et al.
European Journal of Human Genetics : EJHG|July 26, 2000
Giant axonal neuropathy locus refinement to a < 590 kb critical intervalL Cavalier, C BenHamida, R Amouri, et al.
Pageof 3

Showing results (11-20 of 23) with videos related to

Sort By:
Pageof 3
Neuromuscular Disorders : NMD|June 6, 2000
A new locus for autosomal recessive limb-girdle muscular dystrophy in a large consanguineous Tunisian family maps to chromosome 19q13.3A Driss, R Amouri, C Ben Hamida, et al.
Neurology|April 6, 2000
Linkage to chromosome 13q11-12 of an autosomal recessive cerebellar ataxia in a Tunisian familyN Mrissa, S Belal, C B Hamida, et al.
La Revue De Medecine Interne|April 27, 2010
[Axonal neuropathy revealing pleural lymphoma as a long-term outcome of therapeutic pneumothorax]N Fajraoui, K Ben Hamida, A Hadj Kacem, et al.
Neurology|September 15, 2004
Aprataxin gene mutations in Tunisian familiesR Amouri, M-C Moreira, M Zouari, et al.
Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie|April 1, 1996
[Gliotoxic factor and multiple sclerosis]F Rieger, R Amouri, N Benjelloun, et al.
European Journal of Neurology|October 10, 2012
Exome sequencing: an efficient diagnostic tool for complex neurodegenerative disordersM B Hammer, G Eleuch-Fayache, J R Gibbs, et al.
Neurology|April 23, 2003
Fukutin-related protein gene mutated in the original kindred limb-girdle MD 2IA Driss, S Noguchi, R Amouri, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|May 31, 2001
Regenerative capacity of human satellite cells: the mitotic clock in cell transplantationS Di Donna, V Renault, C Forestier, et al.
Journal of the Neurological Sciences|April 30, 1998
A gliotoxic factor and multiple sclerosisA Ménard, R Amouri, T Dobránsky, et al.
European Journal of Human Genetics : EJHG|July 26, 2000
Giant axonal neuropathy locus refinement to a < 590 kb critical intervalL Cavalier, C BenHamida, R Amouri, et al.
Pageof 3