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Neuromuscular Disorders : NMD|December 1, 1996
Limb-girdle muscular dystrophy 2C: clinical aspectsM Ben Hamida, C Ben Hamida, M Zouari, et al.Clinical Neuroscience (New York, N.Y.)|January 1, 1995
Friedreich's ataxia-vitamin E responsive type. The chromosome 8 locusS Belal, F Hentati, C Ben Hamida, 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.Acta Neuropathologica|June 1, 1997
Friedreich's ataxia with isolated vitamin E deficiency: a neuropathological study of a Tunisian patientA Larnaout, S Belal, M Zouari, 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.Revue Neurologique|January 1, 1987
[Multiminicore disease in a rigid spine syndrome]M Ben Hamida, F Hentati, C Ben HamidaBrain : a Journal of Neurology|April 1, 1990
Hereditary motor system diseases (chronic juvenile amyotrophic lateral sclerosis). Conditions combining a bilateral pyramidal syndrome with limb and bulbar amyotrophyM Ben Hamida, F Hentati, C Ben HamidaActa Neuropathologica|January 1, 1994
Clinical and pathological study of three Tunisian siblings with L-2-hydroxyglutaric aciduriaA Larnaout, F Hentati, S Belal, et al.Bulletin De L'Academie Nationale De Medecine|February 1, 1992
[Juvenile amyotrophic lateral sclerosis. Study of 43 cases]M Ben Hamida, F Hentati, C Ben HamidaNeurology|February 1, 1990
Giant axonal neuropathy with inherited multisystem degeneration in a Tunisian kindredM Ben Hamida, F Hentati, C Ben HamidaPageof 28