C. Ben Hamida - Concepedia

Author

C. Ben Hamida

Institut National de Santé Publique

Also Known As

C Ben Hamida, C Hamida, C. Ben Hamida, C.B. Hamida, C.Ben Hamida, CHRISTIANE BEN HAMIDA, S. Oueslati

Publications

1.4K

Citations

H-Index

Concepts

All Affiliations

Institut National de Santé Publique National Institute of Neurology Mongi-Ben Hamida Centre National de la Recherche Scientifique Hopital Universitaire Habib Bourguiba

About

C. Ben Hamida is an author at Institut National de Santé Publique specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	8	8	767
2	Health Sciences	1	1	192
3	Social Sciences	1	1	52
4	Anatomy	1	1	192
5	Emergency Medicine	1	1	15

C. Ben Hamida

Publications

1.3K

Citations

H-Index

Page 1

	Year	Citations
Replicative Potential and Telomere Length in Human Skeletal Muscle: Implications for Satellite Cell-Mediated Gene Therapy Stéphanie Decary, Vincent Mouly, C. Ben Hamida, Human Gene Therapy	1997	298
Shorter telomeres in dystrophic muscle consistent with extensive regeneration in young children Stéphanie Decary, C. Ben Hamida, Vincent Mouly, Neuromuscular Disorders Developmental BiologyKinesiologySkeletal MuscleMotor DevelopmentShorter Telomeres	2000	192
HEREDITARY MOTOR SYSTEM DISEASES (CHRONIC JUVENILE AMYOTROPHIC LATERAL SCLEROSIS) Mongi Ben Hamida, F. Hentati, C. Ben Hamida Brain	1990	171
Safety and efficacy of colistin compared with imipenem in the treatmentof ventilator-associated pneumonia: a matched case–control study Hatem Kallel, Leila Hergafi, Mabrouk Bahloul, Intensive Care Medicine AntibioticsCase–control StudyClinical GastroenterologyInfection ControlUlcerative Colitis	2007	152
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
Prevalence of hospital-acquired infection in a Tunisian hospital Hatem Kallel, M. Bahoul, Hatem Ksibi, Journal of Hospital Infection Tunisian HospitalHealthcare-associated InfectionInfection ControlMedicineHospital Epidemiology	2005	90
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
Homozygosity mapping of giant axonal neuropathy gene to chromosome 16q24.1 C. Ben Hamida, L Cavalier, Samir Belal, Neurogenetics Molecular NeuroscienceNeurogenomicsMendelian DisorderGenetic DisorderNeuroanatomy	1997	52
Phenotype and sarcoglycan expression in Tunisian LGMD 2C patients sharing the same del521-T mutation M. Kéfi, Rim Amouri, Adel Driss, Neuromuscular Disorders Mendelian DisorderAutoimmune DiseaseSarcoglycan ExpressionMedicineGenetic Disorder	2003	43

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