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Journal of the Neurological Sciences|June 1, 1981
[Peroneal atrophy in Tunisia. Study of 70 cases, pure or associated with other heredodegenerative diseases]M Ben Hamida, F Letaief, C Ben Hamida, et al.Journal of the Neurological Sciences|May 1, 1987
Morphometric study of the sensory nerve in classical (or Charcot disease) and juvenile amyotrophic lateral sclerosisM Ben Hamida, F Letaief, F Hentati, 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.Neuromuscular Disorders : NMD|December 1, 1996
Limb-girdle muscular dystrophy 2C: clinical aspectsM Ben Hamida, C Ben Hamida, M Zouari, et al.Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|October 1, 1994
[Congenital fibrolipoma of the mesencephalic protuberation area]A Larnaout, F Hentati, C Ben Hamida, et al.Revue Neurologique|January 1, 1991
[Peripheral neuropathy in a sporadic case of cerebrotendinous xanthomatosis]M Ben Hamida, N Chabbi, 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|January 1, 1994
Clinical and pathological study of three Tunisian siblings with L-2-hydroxyglutaric aciduriaA Larnaout, F Hentati, S Belal, et al.Neuromuscular Disorders : NMD|January 1, 1992
Age-dependent axonal loss in nerve biopsy of patients with xeroderma pigmentosumF Hentati, C Ben Hamida, M Zeghal, et al.Neuromuscular Disorders : NMD|June 19, 1998
LGMD 2E in Tunisia is caused by a homozygous missense mutation in beta-sarcoglycan exon 3C G Bönnemann, J Wong, C Ben Hamida, et al.Pageof 6