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Revue Neurologique|February 1, 1977
[Multiple sclerosis in Tunisia. Clinical study of 100 cases]M B HamidaAnnales D'Oto-Laryngologie Et De Chirurgie Cervico Faciale : Bulletin De La Societe D'Oto-Laryngologie Des Hopitaux De Paris|October 1, 1977
[Multiple sclerosis in Tunisia: cochleo-vestibular study (author's transl)]A Belkahia, M B Hamida, H BouzouitaNeurology|April 13, 2000
Clinical and genetic study of familial Parkinson's disease in TunisiaN Gouider-Khouja, S Belal, M B Hamida, 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.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.Genomics|January 25, 2000
Identification of a new locus for autosomal recessive Charcot-Marie-Tooth disease with focally folded myelin on chromosome 11p15K B Othmane, E Johnson, M Menold, 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.Neurogenetics|May 18, 1999
Refined mapping and characterization of the recessive familial amyotrophic lateral sclerosis locus (ALS2) on chromosome 2q33B A Hosler, P C Sapp, R Berger, et al.Nature Genetics|September 10, 1998
Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophyJ Liu, M Aoki, I Illa, et al.Pageof 1