M. Ben Hamida - Concepedia

Author

M. Ben Hamida

National Institute of Neurology Mongi-Ben Hamida

Also Known As

I. Turki, M B Hamida, M Ben Hamida, M Ben Hamidaa,, M. Ben Hamida, M. Hamida, M.B. Hamida, M.Ben Hamida, Maachou Hamida, Maghraoui Hamida

Publications

3.2K

Citations

H-Index

Concepts

All Affiliations

National Institute of Neurology Mongi-Ben Hamida Inserm Institut National de Santé Publique Hôpital La Rabta Centre National de la Recherche Scientifique

About

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

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	16	18	2.2K
2	Social Sciences	3	3	1.4K
3	Public Health	1	1	27
4	Applied Physiology	1	1	31
5	Cell Biology	1	1	12

M. Ben Hamida

Publications

3.1K

Citations

H-Index

Page 1

	Year	Citations
International Cooperative Ataxia Rating Scale for pharmacological assessment of the cerebellar syndrome P Trouillas, T Takayanagi, Mark Hallett, Journal of the Neurological Sciences Neurobiology Of DiseaseNeurological DisorderClinical NeurologySocial SciencesRehabilitation	1997	1.3K
Localization of Friedreich ataxia phenotype with selective vitamin E deficiency to chromosome 8q by homozygosity mapping Christiane Ben Hamida, Nathalie Doerflinger, Samir Belal, Nature Genetics Mendelian DisorderGenetic DisorderMedicineGeneticsMolecular Biology	1993	210
Linkage of a locus (CMT4A) for autosomal recessive Charcot-Marie-Tooth disease to chromosome 8q Kamel Ben Othmane, F. Hentatl, Felicia Lennon, Human Molecular Genetics	1993	177
Linkage of Miyoshi myopathy (distal autosomal recessive muscular dystrophy) locus to chromosome 2p12-14 Khemissa Bejaoui, Koichi Hirabayashi, Fayçal Hentati, Neurology Miyoshi MyopathyMendelian DisorderFamily MembersGenetic DisorderMedicine	1995	146
Effect of vitamin E supplementation in patients with ataxia with vitamin E deficiency S. Gabsi, N. Gouider‐Khouja, Samir Belal, European Journal of Neurology	2001	144
Friedreich's ataxia phenotype not linked to chromosome 9 and associated with selective autosomal recessive vitamin E deficiency in two inbred Tunisian families M. Ben Hamida, Samir Belal, Giorgio Sirugo, Neurology	1993	136
Prevalence Study of Neurologic Disorders in Kelibia (Tunisia) Neila Attia Romdhane, M. Ben Hamida, Ali Mrabet, Neuroepidemiology	1993	95
Linkage to chromosome 13q11-12 of an autosomal recessive cerebellar ataxia in a Tunisian family Najiba Fekih Mrissa, Samir Belal, C. Ben Hamida, Neurology	2000	80
A new locus for autosomal recessive limb-girdle muscular dystrophy in a large consanguineous Tunisian family maps to chromosome 19q13.3 Adel Driss, Rim Amouri, C. Ben Hamida, Neuromuscular Disorders Rare DiseasesMendelian DisorderGenetic DisorderGeneticsNew Locus	2000	75
Novel mutations in spastin gene and absence of correlation with age at onset of symptoms Afif Hentati, Han‐Xiang Deng, Hong Zhai, Neurology	2000	67

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