Home › Researcher directory › C. Ben Hamida
C. Ben Hamida
Affiliation : Hopital Universitaire Habib Bourguiba · National Institute of Neurology Mongi-Ben Hamida
- 16Publications (affiliation in Tunisia)
- 56Total publications
- 1451Citations
- 15h-index
Research profile
C. Ben Hamida has 16 indexed publications (1980–2008). Their work appears mainly in “Journal des Maladies Vasculaires”, “Annales Françaises d Anesthésie et de Réanimation” and “Intensive Care Medicine”. Their most cited article, “HEREDITARY MOTOR SYSTEM DISEASES (CHRONIC JUVENILE AMYOTROPHIC LATERAL SCLEROSIS)” (1990), has been cited 171 times. 8 of these publications date from the last three years of activity. Their work is co-authored with at least 12 researchers.
Is this you? Get your research seen
Create your free DzCademia profile and add your articles: they will show up more easily on Google and in AI assistants like ChatGPT, so more people can read and cite your work.
Create my free profile Add my publicationsResearch areas
- Muscle Physiology and Disorders
- Urological Disorders and Treatments
- Hereditary Neurological Disorders
- Ureteral procedures and complications
- Pediatric Urology and Nephrology Studies
Publications (16)
- Myocardiopathie du péripartum : incidence, physiopathologie, manifestations cliniques, prise en charge thérapeutique et pronostic
- P153 Syndrome métabolique chez le diabétique type 2, évolution du profil clinique après 5 ans de suivi
- Safety and efficacy of colistin compared with imipenem in the treatmentof ventilator-associated pneumonia: a matched case–control study
- Les microangiopathies thrombotiques. Incidence, physiopathologie, tableau clinique, prise en charge thérapeutique et pronostic
- A good death: another break in the wall
- Stéatose hépatique aiguë gravidique. À propos de 22 cas
- Les microangiopathies thrombotiques en réanimation
- Thrombose post-traumatique de l’artère rénale et déficit en protéine C
- Prevalence of hospital-acquired infection in a Tunisian hospital
- Maladie cœliaque, thrombose veineuse cérébrale et déficit en protéine S, Une association fortuite ?
- Phenotype and sarcoglycan expression in Tunisian LGMD 2C patients sharing the same del521-T mutation
- Linkage to chromosome 13q11-12 of an autosomal recessive cerebellar ataxia in a Tunisian family
- A new locus for autosomal recessive limb-girdle muscular dystrophy in a large consanguineous Tunisian family maps to chromosome 19q13.3
- Homozygosity mapping of giant axonal neuropathy gene to chromosome 16q24.1
- HEREDITARY MOTOR SYSTEM DISEASES (CHRONIC JUVENILE AMYOTROPHIC LATERAL SCLEROSIS)
- Contribution a l'etude quantitative structurale et ultra-structurale de biopsies cutanees et nerveuse dans le diagnostic de l'indifference congenitale a la douleur
Publication venues
- Journal des Maladies Vasculaires × 3
- Annales Françaises d Anesthésie et de Réanimation × 2
- Intensive Care Medicine × 2
- Neuromuscular Disorders × 2
- Diabetes & Metabolism × 1
- Gynécologie Obstétrique & Fertilité × 1
Publications per year
- 20082
- 20072
- 20064
- 20052
- 20031
- 20002
- 19971
- 19901
- 19801
Collaborations
Partner institutions : Institut National de Nutrition et de Technologie Alimentaire · Hopital Universitaire Hedi Chaker · Faculty of Medicine of Sfax
Co-authors
- Hatem Kallel
- Hassen Dammak
- Mabrouk Bahloul
- Mounir Bouaziz
- Hèdi Chelly
- Noureddine Rekik
- Fayçal Hentati
- M. Ben Hamida
- Anis Chaari
- Rim Amouri
- Nadia Khlaf-Bouaziz
- Adel Chaari
Bibliographic data from OpenAlex (open database).
Why choose Dzcademia?
Profiles, articles and conference contributions: give your research a structured public presence. Integrated metadata help search engines and AI assistants identify your work and understand its references.
Comment with Google
Sign in with Google to comment directly on this page.