Accueil › Annuaire des chercheurs › M. Ben Hamida
M. Ben Hamida
Affiliation : Tunis University · Hôpital La Rabta · Faculté de médecine de Tunis · Tunis El Manar University
- 29Publications (affiliation tunisienne)
- 65Publications au total
- 3222Citations
- 26Indice h
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Créer mon profil gratuit Ajouter mes publicationsDomaines de recherche
- 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
Co-auteurs
- 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
Données bibliographiques issues d’OpenAlex (base ouverte).
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