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Showing results (71-80 of 120) with videos related to

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Neurology|August 1, 1987
Extracts of muscle biopsies from patients with spinal muscular atrophies inhibit neurite outgrowth from spinal neuronsC E Henderson, S L Hauser, M Huchet, et al.
Annals of Neurology|November 1, 1992
Childhood peripheral neuropathy with autoantibodies to myelin glycoprotein P0S Ben Jelloun-Dellagi, K Dellagi, D Burger, et al.
Neuromuscular Disorders : NMD|August 26, 1998
Electrophysiology and nerve biopsy: comparative study in Friedreich's ataxia and Friedreich's ataxia phenotype with vitamin E deficiencyM Zouari, M Feki, C Ben Hamida, et al.
Neurology|September 15, 2004
Aprataxin gene mutations in Tunisian familiesR Amouri, M-C Moreira, M Zouari, et al.
Revue Neurologique|March 24, 2004
[Lateral gaze palsy and progressive scoliosis in 4 Tunisian families]F El Bahri-Ben Mrad, N Gouider-Khouja, S Gabsi, et al.
Journal of Inherited Metabolic Disease|January 1, 1993
Familial encephalopathy and L-2-hydroxyglutaric aciduriaN Kaabachi, A Larnaout, D Rabier, et al.
European Journal of Neurology|October 11, 2014
The role of SNCA and MAPT in Parkinson disease and LRRK2 parkinsonism in the Tunisian Arab-Berber populationJ Trinh, E K Gustavsson, I Guella, et al.
Experimental Gerontology|October 29, 2000
Skeletal muscle regeneration and the mitotic clockV Renault, G Piron-Hamelin, C Forestier, et al.
Neurogenetics|May 18, 1999
Fine localization of the CMT4A locus using a PAC contig and haplotype analysisK Ben Othmane, J M Rochelle, M Ben Hamida, et al.
Nature Genetics|February 1, 1995
Ataxia with isolated vitamin E deficiency is caused by mutations in the alpha-tocopherol transfer proteinK Ouahchi, M Arita, H Kayden, et al.
Pageof 12

Showing results (71-80 of 120) with videos related to

Sort By:
Pageof 12
Neurology|August 1, 1987
Extracts of muscle biopsies from patients with spinal muscular atrophies inhibit neurite outgrowth from spinal neuronsC E Henderson, S L Hauser, M Huchet, et al.
Annals of Neurology|November 1, 1992
Childhood peripheral neuropathy with autoantibodies to myelin glycoprotein P0S Ben Jelloun-Dellagi, K Dellagi, D Burger, et al.
Neuromuscular Disorders : NMD|August 26, 1998
Electrophysiology and nerve biopsy: comparative study in Friedreich's ataxia and Friedreich's ataxia phenotype with vitamin E deficiencyM Zouari, M Feki, C Ben Hamida, et al.
Neurology|September 15, 2004
Aprataxin gene mutations in Tunisian familiesR Amouri, M-C Moreira, M Zouari, et al.
Revue Neurologique|March 24, 2004
[Lateral gaze palsy and progressive scoliosis in 4 Tunisian families]F El Bahri-Ben Mrad, N Gouider-Khouja, S Gabsi, et al.
Journal of Inherited Metabolic Disease|January 1, 1993
Familial encephalopathy and L-2-hydroxyglutaric aciduriaN Kaabachi, A Larnaout, D Rabier, et al.
European Journal of Neurology|October 11, 2014
The role of SNCA and MAPT in Parkinson disease and LRRK2 parkinsonism in the Tunisian Arab-Berber populationJ Trinh, E K Gustavsson, I Guella, et al.
Experimental Gerontology|October 29, 2000
Skeletal muscle regeneration and the mitotic clockV Renault, G Piron-Hamelin, C Forestier, et al.
Neurogenetics|May 18, 1999
Fine localization of the CMT4A locus using a PAC contig and haplotype analysisK Ben Othmane, J M Rochelle, M Ben Hamida, et al.
Nature Genetics|February 1, 1995
Ataxia with isolated vitamin E deficiency is caused by mutations in the alpha-tocopherol transfer proteinK Ouahchi, M Arita, H Kayden, et al.
Pageof 12