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M. Ben Hamida
Affiliation : Tunis University · Hôpital La Rabta · Faculté de médecine de Tunis · Tunis El Manar University
- 29Publications (affiliation in Tunisia)
- 65Total publications
- 3222Citations
- 26h-index
Research profile
M. Ben Hamida has 29 indexed publications (1987–2026). Their work appears mainly in “Neuromuscular Disorders”, “Neurology” and “Acta Neuropathologica”. Their most cited article, “International Cooperative Ataxia Rating Scale for pharmacological assessment of the cerebellar syndrome” (1997), has been cited 1266 times. 3 of these publications date from the last three years of activity. Their work is co-authored with at least 12 researchers, including institutions in France, United States, Germany.
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Create my free profile Add my publicationsResearch areas
- Hereditary Neurological Disorders
- Genetic Neurodegenerative Diseases
- Muscle Physiology and Disorders
- Neurogenetic and Muscular Disorders Research
- Genomics and Rare Diseases
Publications (29)
- Associated Factors for Adhesions Post Surgery: A Case Control Study
- Associated factors for postoperative morbidity and mortality following surgery of obstructive colon tumors
- Validation of the diagnostic score for acute pancreatitis: a prospective study
- Phenotype and sarcoglycan expression in Tunisian LGMD 2C patients sharing the same del521-T mutation
- Effect of vitamin E supplementation in patients with ataxia with vitamin E deficiency
- Wernicke's encephalopathy in a patient with Crohn's disease: a pathological study
- 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
- Clinical and genetic study of familial Parkinson’s disease in Tunisia
- Electrophysiological and nerve biopsy: comparative study in Friedreich's ataxia and Friedreich's ataxia phenotype with vitamin E deficiency
- LGMD 2E in Tunisia is caused by a homozygous missense mutation in β-sarcoglycan exon 3
- Atypical ataxia telangiectasia with early childhood lower motor neuron degeneration: a clinicopathological observation in three siblings
- International Cooperative Ataxia Rating Scale for pharmacological assessment of the cerebellar syndrome
- Homozygosity mapping of giant axonal neuropathy gene to chromosome 16q24.1
- Friedreich's ataxia with isolated vitamin E deficiency: a neuropathological study of a Tunisian patient
- Limb-girdle muscular dystrophy 2C: Clinical aspects
- Recessive Schwartz-Jampel syndrome (SJS): confirmation of linkage to chromosome 1p, evidence of genetic homogeneity and reduction of the SJS locus to a 3-cM interval
- Physical and Genetic Mapping of the CMT4A Locus and Exclusion of PMP-2 as the Defect in CMT4A
- Clinical and genetic analysis of a Tunisian family with autosomal dominant cerebellar ataxia type 1linked to the SCA2 locus
- Clinical and pathological study of three Tunisian siblings with L-2-hydroxyglutaric aciduria
- Expression of myosin isoforms and of desmin, vimentin and titin in Tunisian Duchenne-like autosomal recessive muscular dystrophy
- Linkage of a locus (CMT4A) for autosomal recessive Charcot-Marie-Tooth disease to chromosome 8q
- Friedreich's ataxia phenotype not linked to chromosome 9 and associated with selective autosomal recessive vitamin E deficiency in two inbred Tunisian families
- Familial encephalopathy and l ‐2‐hydroxyglutaric aciduria
- Childhood peripheral neuropathy with autoantibodies to myelin glycoprotein Po
- Juvenile amyotrophic lateral sclerosis and related syndromes.
- [Schwartz-Jampel syndrome. Clinical and histopathological study of 4 cases].
- Presence of normal dystrophin in Tunisian severe childhood autosomal recessive muscular dystrophy
- Hypertrophic neuropathy in spinocerebellar degeneration
Publication venues
- Neuromuscular Disorders × 5
- Neurology × 5
- Acta Neuropathologica × 3
- F1000Research × 2
- Journal of Neurology × 2
- Journal of the Neurological Sciences × 2
Publications per year
- 20261
- 20252
- 20031
- 20012
- 20003
- 19983
- 19973
- 19962
- 19951
- 19943
Collaborations
Partner institutions : National Institute of Neurology Mongi-Ben Hamida · Inserm · Centre National de la Recherche Scientifique · Cyprus Institute of Neurology and Genetics · Düsseldorf University Hospital
Co-authors’ countries : France · United States · Germany
Co-authors
- Fayçal Hentati
- Samir Belal
- Christiane Ben Hamida
- Abdelmajid Larnaout
- C. Ben Hamida
- Mestiri Souhir
- Trifa Fatma
- Rami Guizani
- Siala Rakia
- Ilhem Turki
- Ch. Ben Hamida
- Mourad Zouari
Bibliographic data from OpenAlex (open database).
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