Mongi Ben Hamida - Concepedia

Author

Mongi Ben Hamida

National Institute of Neurology Mongi-Ben Hamida

Also Known As

MONGI BEN HAMIDA, Mongi Ben Hamida

Publications

Citations

H-Index

Concepts

All Affiliations

National Institute of Neurology Mongi-Ben Hamida Institut National de Santé Publique Duke Medical Center Duke University Hospital Inserm

About

Mongi Ben Hamida is an author at National Institute of Neurology Mongi-Ben Hamida specializing in medicine, genetics, and neurology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	14	16	2.7K
2	Health Sciences	1	1	27
3	Social Sciences	1	1	22
4	Biochemistry	1	1	18
5	Cell Biology	1	1	367

Mongi Ben Hamida

Publications

3.8K

Citations

H-Index

Page 1

	Year	Citations
Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophy Jing Liu, Masashi Aoki, Isabel Illa, Nature Genetics Miyoshi MyopathyRare DiseasesMendelian DisorderSkeletal MuscleGenetic Disorder	1998	914
Ataxia with isolated vitamin E deficiency is caused by mutations in the α–tocopherol transfer protein Karim Ouahchi, Makoto Arita, Herbert J. Kayden, Nature Genetics Genetic DisorderGeneticsInherited Metabolic DiseasePathologyα–Tocopherol Transfer Protein	1995	563
Mutations in the Dystrophin-Associated Protein γ-Sarcoglycan in Chromosome 13 Muscular Dystrophy S. Noguchi, Elizabeth M. McNally, Kamel Ben Othmane, Science	1995	507
Ganglioside-induced differentiation-associated protein-1 is mutant in Charcot-Marie-Tooth disease type 4A/8q21 Rachel V. Baxter, Kamel Ben Othmane, Julie M. Rochelle, Nature Genetics Disease MechanismPathogenesisExperimental PathologyPathologyDegenerative Disease	2001	367
Severe childhood muscular dystrophy affecting both sexes and frequent in tunisia Mongi Ben Hamida, Michel Fardeau, N. Attia Muscle & Nerve	1983	177
Linkage of Tunisian autosomal recessive Duchenne–like muscular dystrophy to the pericentromeric region of chromosome 13q Kamel Ben Othmane, Mongi Ben Hamida, Margaret A. Pericak‐Vance, Nature Genetics Chromosome DynamicsDevelopmental BiologyMendelian DisorderCytogeneticsMedicine	1992	175
HEREDITARY MOTOR SYSTEM DISEASES (CHRONIC JUVENILE AMYOTROPHIC LATERAL SCLEROSIS) Mongi Ben Hamida, F. Hentati, C. Ben Hamida Brain	1990	171
Linkage of a commoner form of recessive amyotrophic lateral sclerosis to chromosome 15q15-q22 markers Afif Hentati, Karim Ouahchi, Margaret A. Pericak‐Vance, Neurogenetics Amyotrophic Lateral SclerosisMendelian DisorderGenetic DisorderCommoner FormGenetics	1998	169
Localization of α-tocopherol transfer protein in the brains of patients with ataxia with vitamin E deficiency and other oxidative stress related neurodegenerative disorders Richard P. Copp, Fayçal Hentati, A. Larnaout, Brain Research	1999	128
Linkage of a locus for autosomal dominant familial spastic paraplegia to chromosome 2p markers Afif Hentati, Margaret A. Pericak‐Vance, Felicia Lennon, Human Molecular Genetics Down SyndromeMendelian DisorderGenetic DisorderGeneticsInherited Spg	1994	108

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