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Mongi Ben Hamida
Affiliation : National Institute of Neurology Mongi-Ben Hamida
- 19Publications (affiliation in Tunisia)
- 31Total publications
- 4068Citations
- 21h-index
Research profile
Mongi Ben Hamida has 19 indexed publications (1981–2003). Their work appears mainly in “Nature Genetics”, “Neurogenetics” and “Human Molecular Genetics”. Their most cited article, “Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophy” (1998), has been cited 919 times. 2 of these publications date from the last three years of activity. Their work is co-authored with at least 12 researchers.
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Create my free profile Add my publicationsResearch areas
- Hereditary Neurological Disorders
- Genetic Neurodegenerative Diseases
- Muscle Physiology and Disorders
- Amyotrophic Lateral Sclerosis Research
- Genomics and Rare Diseases
Publications (19)
- Autosomal recessive parkinsonism linked to parkin gene in a Tunisian family. Clinical, genetic and pathological study
- Serum Vitamin E and Lipid-adjusted Vitamin E Assessment in Friedreich Ataxia Phenotype Patients and Unaffected Family Members
- Giant axonal neuropathy locus refinement to a < 590 kb critical interval
- Identification of a New Locus for Autosomal Recessive Charcot–Marie–Tooth Disease with Focally Folded Myelin on Chromosome 11p15
- Dysferlin, a novel skeletal muscle gene, is mutated in Miyoshi myopathy and limb girdle muscular dystrophy
- Linkage of a commoner form of recessive amyotrophic lateral sclerosis to chromosome 15q15-q22 markers
- Refined mapping and characterization of the recessive familial amyotrophic lateral sclerosis locus ( ALS2 ) on chromosome 2q33
- Mutations in the Dystrophin-Associated Protein γ-Sarcoglycan in Chromosome 13 Muscular Dystrophy
- Localization of the Schwartz–Jampel syndrome (SJS) locus to chromosome 1p34–p36.1 by homozygosity mapping
- Linkage of recessive familial amyotrophic lateral sclerosis to chromosome 2q33–q35
- Linkage of a locus for autosomal dominant familial spastic paraplegia to chromosome 2p markers
- Biochemical and immunocytochemical analysis in chronic proximal spinal muscular atrophy
- Phenylketonuria: An Underlying Etiology of Autistic Syndrome. A Case Report
- Age-dependent axonal loss in nerve biopsy of patients with xeroderma pigmentosum
- Duchenne muscular dystrophy in Tunisia: A clinical and morphological study of 77 cases
- HEREDITARY MOTOR SYSTEM DISEASES (CHRONIC JUVENILE AMYOTROPHIC LATERAL SCLEROSIS)
- Giant axonal neuropathy with inherited multisystem degeneration in a Tunisian kindred
- Letters to the editor
- Les atrophies péronières en Tunisie
Publication venues
- Nature Genetics × 2
- Neurogenetics × 2
- Human Molecular Genetics × 2
- Muscle & Nerve × 2
- Journal of the Neurological Sciences × 2
- Parkinsonism & Related Disorders × 1
Publications per year
- 20031
- 20021
- 20001
- 19991
- 19983
- 19952
- 19943
- 19923
- 19902
- 19891
Collaborations
Partner institutions : Hôpital La Rabta · Faculté de médecine de Tunis · Hôpital Charles-Nicolle · Tunis University · Tunis El Manar University
Co-authors
- Fayçal Hentati
- Christiane Ben Hamida
- Samir Belal
- Najoua Miladi
- Rim Amouri
- Abdelmajid Larnaout
- Ilhem Turki
- C. Ben Hamida
- Fethi Letaief
- Sana Sfar
- Malek Souissi
- Mohamed Ridha Kamoun
Bibliographic data from OpenAlex (open database).
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