Mongi Ben Hamida
Institut National de Santé Publique(TN)
Publications by Year
Research Areas
Neurological diseases and metabolism, Hereditary Neurological Disorders, Muscle Physiology and Disorders, Neurogenetic and Muscular Disorders Research, Amyotrophic Lateral Sclerosis Research
Most-Cited Works
- → Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophy(1998)916 cited
- → Ataxia with isolated vitamin E deficiency is caused by mutations in the α–tocopherol transfer protein(1995)567 cited
- → Mutations in the Dystrophin-Associated Protein γ-Sarcoglycan in Chromosome 13 Muscular Dystrophy(1995)507 cited
- → Ganglioside-induced differentiation-associated protein-1 is mutant in Charcot-Marie-Tooth disease type 4A/8q21(2001)368 cited
- → Linkage of recessive familial amyotrophic lateral sclerosis to chromosome 2q33–q35(1994)205 cited
- → Severe childhood muscular dystrophy affecting both sexes and frequent in tunisia(1983)177 cited
- → Linkage of Tunisian autosomal recessive Duchenne–like muscular dystrophy to the pericentromeric region of chromosome 13q(1992)175 cited
- → HEREDITARY MOTOR SYSTEM DISEASES (CHRONIC JUVENILE AMYOTROPHIC LATERAL SCLEROSIS)(1990)171 cited
- → Linkage of a commoner form of recessive amyotrophic lateral sclerosis to chromosome 15q15-q22 markers(1998)169 cited
- → Localization of α-tocopherol transfer protein in the brains of patients with ataxia with vitamin E deficiency and other oxidative stress related neurodegenerative disorders(1999)128 cited