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C. Ben Hamida
Observed names:
C Ben Hamida,
C Hamida,
C. BEN HAMIDA,
C.B. Hamida,
C.Ben Hamida,
CHRISTIANE BEN HAMIDA
show all 6
Observed institutions:
Harvard University,
Hôpital La Rabta,
Institut National de Nutrition et de Technologie Alimentaire,
Wolters Kluwer Health,
National Institute of Neurology Mongi-Ben Hamida,
Hopital Universitaire Habib Bourguiba
show all 6
OpenAlex ID:
A5111522083
Replicative Potential and Telomere Length in Human Skeletal Muscle: Implications for Satellite Cell-Mediated Gene Therapy
1997
·
S. Decary
, V. Mouly
, et al.
·
Human Gene Therapy
·
304
Shorter telomeres in dystrophic muscle consistent with extensive regeneration in young children
2000
·
S. Decary
, C. Ben Hamida
, et al.
·
Neuromuscular Disorders
·
195
Hereditary Motor System Diseases (chronic Juvenile Amyotrophic Lateral Sclerosis)
1990
·
MONGI BEN HAMIDA
, FAYÇAL HENTATI
, et al.
·
Brain
·
171
Safety and efficacy of colistin compared with imipenem in the treatmentof ventilator-associated pneumonia: a matched case–control study
2007
·
H. Kallel
, L. Hergafi
, et al.
·
Intensive Care Medicine
·
153
Linkage of Miyoshi myopathy (distal autosomal recessive muscular dystrophy) locus to chromosome 2p12-14
1995
·
K. Bejaoui
, K. Hirabayashi
, et al.
·
Neurology
·
146
Prevalence of hospital-acquired infection in a Tunisian hospital
2005
·
H. Kallel
, M. Bahoul
, et al.
·
Journal of Hospital Infection
·
92
Linkage to chromosome 13q11-12 of an autosomal recessive cerebellar ataxia in a Tunisian family
2000
·
N. Mrissa
, S. Belal
, et al.
·
Neurology
·
79
A new locus for autosomal recessive limb-girdle muscular dystrophy in a large consanguineous Tunisian family maps to chromosome 19q13.3
2000
·
A. Driss
, R. Amouri
, et al.
·
Neuromuscular Disorders
·
75
Homozygosity mapping of giant axonal neuropathy gene to chromosome 16q24.1
1997
·
C.B. Hamida
, L. Cavalier
, et al.
·
Neurogenetics
·
52
Phenotype and sarcoglycan expression in Tunisian LGMD 2C patients sharing the same del521-T mutation
2003
·
M Kefi
, R Amouri
, et al.
·
Neuromuscular Disorders
·
44
A good death: another break in the wall
2006
·
H. Kallel
, H. Dammak
, et al.
·
Intensive Care Medicine
·
22
Myocardiopathie du péripartum : incidence, physiopathologie, manifestations cliniques, prise en charge thérapeutique et pronostic
2008
·
M. Bahloul
, M.N. Ben Ahmed
, et al.
·
Annales Françaises d Anesthésie et de Réanimation
·
21
Maladie cœliaque, thrombose veineuse cérébrale et déficit en protéine S, Une association fortuite ?
2005
·
M. Bahloul
, A. Chaari
, et al.
·
Journal des Maladies Vasculaires
·
19
Evolution of muscle specific proteins in Werdnig-Hoffman's disease
1992
·
N. Soussi-Yanicostas
, C.Ben Hamida
, et al.
·
Journal of the Neurological Sciences
·
17
[Hemolytic-uremic syndrome secondary to scorpion envenomation (apropos of 2 cases)].
2004
·
M Bahloul
, M Ben Hmida
, et al.
·
PubMed
·
15
Fourth meeting of the European Neurological Society 25–29 June 1994 Barcelona, Spain
1994
·
The European Velnacrine Study Group
, L. Harms
, et al.
·
Journal of Neurology
·
13
Stéatose hépatique aiguë gravidique. À propos de 22 cas
2006
·
M. Bahloul
, H. Dammak
, et al.
·
Gynécologie Obstétrique & Fertilité
·
8
[Multiminicore disease in a rigid spine syndrome].
1987
·
M Ben Hamida
, F Hentati
, et al.
·
PubMed
·
8
Insulinaemia after grave envenomation by scorpion stings (GESS)
1996
·
M. Bouaziz
, M. Bellasoued
, et al.
·
Toxicon
·
5
Les microangiopathies thrombotiques. Incidence, physiopathologie, tableau clinique, prise en charge thérapeutique et pronostic
2007
·
M. Bahloul
, H. Dammak
, et al.
·
Journal des Maladies Vasculaires
·
3
Les microangiopathies thrombotiques en réanimation
2006
·
M. Bahloul
, C. Ben Hamida
, et al.
·
Annales Françaises d Anesthésie et de Réanimation
·
3
Thrombose post-traumatique de l’artère rénale et déficit en protéine C
2006
·
M. Bahloul
, D. Abid
, et al.
·
Journal des Maladies Vasculaires
·
1
Linkage to Chromosome 13q11‐12 of an Autosomal Recessive Cerebellar Ataxia in a Tunisian Family
2000
·
N Mrissa
, S Belal
, et al.
·
Journal of the Peripheral Nervous System
·
1
LGMD 2E in Tunisia is caused by a missense mutation Arg91Leu in β-sarcoglycan
1997
·
C. Bönnemann
, J. Wong
, et al.
·
Neuromuscular Disorders
·
1
Study of atrio-ventricular conduction by registration of his potential after grave envenomation by scorpion stings (GESS)
1996
·
M. Bouaziz
, C. Ben Hamida
, et al.
·
Toxicon
·
1
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Works count:
56
Citation count:
1,452
H-index:
15
I10-index:
16
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