Samir Belal - Concepedia

Author

Samir Belal

National Institute of Neurology Mongi-Ben Hamida

Also Known As

C. Ramo-Tello, S Belal, S. Belal, Samir Belal, samir Belal

120

Publications

2.9K

Citations

H-Index

Concepts

All Affiliations

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

About

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

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	15	21	1.4K
2	Social Sciences	6	6	600
3	Public Health	2	2	30
4	Applied Physiology	1	1	31
5	Biology	1	1	45

Samir Belal

Publications

2.7K

Citations

H-Index

Page 1

	Year	Citations
The gene encoding gigaxonin, a new member of the cytoskeletal BTB/kelch repeat family, is mutated in giant axonal neuropathy Pascale Bomont, L Cavalier, F Blondeau, Nature Genetics NeuroregenerationMolecular NeuroscienceGiant Axonal NeuropathyNeuroanatomyExperimental Neuropathology	2000	410
Molecular and Clinical Correlations in Spinocerebellar Ataxia 2: A Study of 32 Families Alexandra Dürr, Olivier Didierjean, G. Imbert, Human Molecular Genetics	1997	256
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 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
Linkage of ‘pure’ autosomal recessive familial spastic paraplegia to chromosome 8 markers and evidence of genetic locus heterogeneity Afif Hentati, M.A. Perlcak-Vance, Wu-Yen Hung, Human Molecular Genetics	1994	132
Phenotypic Features and Genetic Findings in Sacsin-Related Autosomal Recessive Ataxia in Tunisia Ghada El Euch-Fayache, Irfan Lalani, Rim Amouri, Archives of Neurology	2003	107
De Novo Expansion of Intermediate Alleles in Spinocerebellar Ataxia 7 Giovanni Stévanin, Paola Giunti, Gilles David, Human Molecular Genetics	1998	100
Autosomal recessive parkinsonism linked to parkin gene in a Tunisian family. Clinical, genetic and pathological study N. Gouider‐Khouja, A. Larnaout, Rim Amouri, Parkinsonism & Related Disorders Neurodegenerative DiseasesGenetic DisorderGeneticsParkinson DiseaseAutosomal Recessive Parkinsonism	2003	92

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