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Mongi Ben Hamida

Affiliations: 
Neurology Institut National de Neurologie, Tunis, Tunis, Tunisia 
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"Mongi Hamida"
Mean distance: 18.03 (cluster 3)
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Parents

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Raymond Garcin grad student Institut National de Neurologie

Children

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Fayçal Hentati grad student Institut National de Neurologie

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Publications

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Feki M, Belal S, Feki H, et al. (2002) Serum Vitamin E and Lipid-adjusted Vitamin E Assessment in Friedreich Ataxia Phenotype Patients and Unaffected Family Members Clinical Chemistry. 48: 577-579
Larnaout A, El-Euch G, Kchir N, et al. (2001) Wernicke's encephalopathy in a patient with Crohn's disease: a pathological study. Journal of Neurology. 248: 57-60
Cavalier L, BenHamida C, Amouri R, et al. (2000) Giant axonal neuropathy locus refinement to a < 590 kb critical interval. European Journal of Human Genetics : Ejhg. 8: 527-34
Gouider-Khouja N, Belal S, Hamida MB, et al. (2000) Clinical and genetic study of familial Parkinson's disease in Tunisia. Neurology. 54: 1603-9
Mrissa N, Belal S, Hamida CB, et al. (2000) Linkage to chromosome 13q11-12 of an autosomal recessive cerebellar ataxia in a Tunisian family. Neurology. 54: 1408-14
Othmane KB, Johnson E, Menold M, et al. (1999) Identification of a new locus for autosomal recessive Charcot-Marie-Tooth disease with focally folded myelin on chromosome 11p15. Genomics. 62: 344-9
Hosler BA, Sapp PC, Berger R, et al. (1998) Refined mapping and characterization of the recessive familial amyotrophic lateral sclerosis locus (ALS2) on chromosome 2q33. Neurogenetics. 2: 34-42
Liu J, Aoki M, Illa I, et al. (1998) Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophy. Nature Genetics. 20: 31-6
Bönnemann CG, Wong J, Ben Hamida C, et al. (1998) LGMD 2E in Tunisia is caused by a homozygous missense mutation in beta-sarcoglycan exon 3. Neuromuscular Disorders : Nmd. 8: 193-7
Othmane KB, Rochelle JM, Johnson E, et al. (1997) Clinical and genetic aspects of autosomal recessive CMT Neuromuscular Disorders. 7: 464-465
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