Home › Researcher directory › Ch. Ben Hamida

Ch. Ben Hamida

Affiliation : Hopital Universitaire Habib Bourguiba

4Publications (affiliation in Tunisia)
8Total publications
96Citations
4h-index

Research profile

Ch. Ben Hamida has 4 indexed publications (1990–2016). Their work appears mainly in “Neuromuscular Disorders”, “La Revue de Médecine Interne” and “Neurology”. Their most cited article, “LGMD 2E in Tunisia is caused by a homozygous missense mutation in β-sarcoglycan exon 3” (1998), has been cited 31 times. Their work is co-authored with at least 12 researchers, including institutions in France.

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 publications

Research areas

Muscle Physiology and Disorders
Genomics and Rare Diseases
Cardiomyopathy and Myosin Studies
Genetic Neurodegenerative Diseases
Venomous Animal Envenomation and Studies

Publications (4)

Actualité sur le syndrome HELLP (Hemolysis, Elevated Liver enzymes and Low Platelets)
2016 · La Revue de Médecine Interne · cited 6 times
LGMD 2E in Tunisia is caused by a homozygous missense mutation in β-sarcoglycan exon 3
1998 · Neuromuscular Disorders · cited 31 times
Limb-girdle muscular dystrophy 2C: Clinical aspects
1996 · Neuromuscular Disorders · cited 31 times
Presence of normal dystrophin in Tunisian severe childhood autosomal recessive muscular dystrophy
1990 · Neurology · cited 28 times

Publication venues

Neuromuscular Disorders × 2
La Revue de Médecine Interne × 1
Neurology × 1

Publications per year

20161
19981
19961
19901

Collaborations

Partner institutions : Inserm · Faculté de médecine de Tunis · National Institute of Neurology Mongi-Ben Hamida

Co-authors’ countries : France

Co-authors

Bibliographic data from OpenAlex (open database).