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F Hentati

Showing results (31-40 of 120) with videos related to

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La Tunisie Medicale|March 24, 2000
[Vermian agenesis: Report of a family and review of the literature]S Gabsi, N Gouider-Khouja, I Mili-Boussen, et al.
Neuromuscular Disorders : NMD|December 1, 1996
Limb-girdle muscular dystrophy 2C: clinical aspectsM Ben Hamida, C Ben Hamida, M Zouari, et al.
Neuromuscular Disorders : NMD|April 19, 2005
Allelic heterogeneity of GNE gene mutation in two Tunisian families with autosomal recessive inclusion body myopathyR Amouri, A Driss, K Murayama, et al.
Neuroradiology|June 29, 2000
Nasu-Hakola disease in two Tunisian siblings: new radiological findingsM Chaabane, A Larnaout, R Sebai, et al.
Journal of Neurology|May 20, 1998
Atypical ataxia telangiectasia with early childhood lower motor neuron degeneration: a clinicopathological observation in three siblingsA Larnaout, S Belal, C Ben Hamida, et al.
Clinical and Experimental Rheumatology|January 1, 1996
High levels of bcl-2 protein in the T lymphocytes of patients with Behçet's diseaseA Hamzaoui, K Hamzaoui, C Kooli, et al.
Revue Neurologique|January 1, 1988
[Chronic proximal spinal amyotrophies in Tunisia. Clinical, genetic, epidemiologic and histopathologic study]M Ben Hamida, F Hentati, N Chebbi, et al.
Revue Neurologique|January 1, 1991
[Clinical and genetic analysis of 188 families with spinocerebellar degeneration. Friedreich's disease and P. Marie's hereditary ataxias]M Ben Hamida, N Attia-Romdhane, C H Triki, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|June 18, 2011
Microscopic polyangiitis presenting with peripheral and central neurological manifestationsS Ben Sassi, I Ben Ghorbel, H Mizouni, et al.
Journal of Child Neurology|October 31, 1998
Dihydropteridine reductase deficiency in a large consanguineous Tunisian family: clinical, biochemical, and neuropathologic findingsN Miladi, A Larnaout, J L Dhondt, et al.
Pageof 12

Showing results (31-40 of 120) with videos related to

Sort By:
Pageof 12
La Tunisie Medicale|March 24, 2000
[Vermian agenesis: Report of a family and review of the literature]S Gabsi, N Gouider-Khouja, I Mili-Boussen, et al.
Neuromuscular Disorders : NMD|December 1, 1996
Limb-girdle muscular dystrophy 2C: clinical aspectsM Ben Hamida, C Ben Hamida, M Zouari, et al.
Neuromuscular Disorders : NMD|April 19, 2005
Allelic heterogeneity of GNE gene mutation in two Tunisian families with autosomal recessive inclusion body myopathyR Amouri, A Driss, K Murayama, et al.
Neuroradiology|June 29, 2000
Nasu-Hakola disease in two Tunisian siblings: new radiological findingsM Chaabane, A Larnaout, R Sebai, et al.
Journal of Neurology|May 20, 1998
Atypical ataxia telangiectasia with early childhood lower motor neuron degeneration: a clinicopathological observation in three siblingsA Larnaout, S Belal, C Ben Hamida, et al.
Clinical and Experimental Rheumatology|January 1, 1996
High levels of bcl-2 protein in the T lymphocytes of patients with Behçet's diseaseA Hamzaoui, K Hamzaoui, C Kooli, et al.
Revue Neurologique|January 1, 1988
[Chronic proximal spinal amyotrophies in Tunisia. Clinical, genetic, epidemiologic and histopathologic study]M Ben Hamida, F Hentati, N Chebbi, et al.
Revue Neurologique|January 1, 1991
[Clinical and genetic analysis of 188 families with spinocerebellar degeneration. Friedreich's disease and P. Marie's hereditary ataxias]M Ben Hamida, N Attia-Romdhane, C H Triki, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|June 18, 2011
Microscopic polyangiitis presenting with peripheral and central neurological manifestationsS Ben Sassi, I Ben Ghorbel, H Mizouni, et al.
Journal of Child Neurology|October 31, 1998
Dihydropteridine reductase deficiency in a large consanguineous Tunisian family: clinical, biochemical, and neuropathologic findingsN Miladi, A Larnaout, J L Dhondt, et al.
Pageof 12