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Mongi Ben Hamida

Research Profile

Geographic Areas

Tunisia

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Disorders

Genes & Molecular Sequences

Recessive Genes

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Anatomy

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Publications

TOP 3
Mounir Kefi; Rim Amouri; Adel Driss; Christiane Ben Hamida; Mongi Ben Hamida; Louis Kunkel; Faycal Hentati
Phenotype and sarcoglycan expression in Tunisian LGMD 2C patients sharing the same del521-T mutation.
Neziha Gouider-Khouja; Abdelmajid Larnaout; Rim Amouri; Sana Sfar; Samir Belal; Christiane Ben Hamida; Mongi Ben Hamida; Nobutaka Hattori; Yoshikuni Mizuno; Faycal Hentati
Autosomal recessive parkinsonism linked to parkin gene in a Tunisian family. Clinical, genetic and pathological study.
Moncef Feki; Samir Belal; Habib Feki; Malek Souissi; Mahbouba Frih-Ayed; Neziha Kaabachi; Faycal Hentati; Mongi Ben Hamida; Abderraouf Mebazaa
Serum vitamin E and lipid-adjusted vitamin E assessment in Friedreich ataxia phenotype patients and unaffected family members.

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All Publications

2003: Mounir Kefi; Rim Amouri; Adel Driss; Christiane Ben Hamida; Mongi Ben Hamida; Louis Kunkel; Faycal Hentati
Phenotype and sarcoglycan expression in Tunisian LGMD 2C patients sharing the same del521-T mutation.
Neuromuscular disorders : NMD 2003;13(10):779-87.
2003: Neziha Gouider-Khouja; Abdelmajid Larnaout; Rim Amouri; Sana Sfar; Samir Belal; Christiane Ben Hamida; Mongi Ben Hamida; Nobutaka Hattori; Yoshikuni Mizuno; Faycal Hentati
Autosomal recessive parkinsonism linked to parkin gene in a Tunisian family. Clinical, genetic and pathological study.
Parkinsonism & related disorders 2003;9(5):247-51.
2002: Moncef Feki; Samir Belal; Habib Feki; Malek Souissi; Mahbouba Frih-Ayed; Neziha Kaabachi; Faycal Hentati; Mongi Ben Hamida; Abderraouf Mebazaa
Serum vitamin E and lipid-adjusted vitamin E assessment in Friedreich ataxia phenotype patients and unaffected family members.
Clinical chemistry 2002;48(3):577-9.
2002: Rachel V Baxter; Kamel Ben Othmane; Julie M Rochelle; Jason E Stajich; Christine M Hulette; Susan Dew-Knight; Faycal Hentati; Mongi Ben Hamida; S Bel; Judith E Stenger; John Gilbert; Margaret Pericak-Vance; Jeffery Vance
Ganglioside-induced differentiation-associated protein-1 is mutant in Charcot-Marie-Tooth disease type 4A/8q21.
Nature genetics 2002;30(1):21-2.
2001: Y Yang; A Hentati; H X Deng; Omar Dabbagh; T Sasaki; M Hirano; Wu-Yen Hung; Karim Ouahchi; J Yan; anser azim; N Cole; GG Gascon; A Yagmour; Mongi Ben Hamida; Margaret Pericak-Vance; Faycal Hentati; Teepu Siddique
The gene encoding alsin, a protein with three guanine-nucleotide exchange factor domains, is mutated in a form of recessive amyotrophic lateral sclerosis.
Nature genetics 2001;29(2):160-5.
2001: S Gabsi; Neziha Gouider-Khouja; Samir Belal; M Fki; Mounir Kefi; Ilhem Turki; Mongi Ben Hamida; HJ Kayden; R Mebazaa; Faycal Hentati
Effect of vitamin E supplementation in patients with ataxia with vitamin E deficiency.
European journal of neurology : the official journal of the European Federation of Neurological Societies 2001;8(5):477-81.
2001: C Barhoumi; Rim Amouri; Christiane Ben Hamida; Mongi Ben Hamida; Salem Machghoul; M Gueddiche; Faycal Hentati
Linkage of a new locus for autosomal recessive axonal form of Charcot-Marie-Tooth disease to chromosome 8q21.3.
Neuromuscular disorders : NMD 2001;11(1):27-34.
2000: A Hentati; Han-Xiang Deng; H Zhai; W Chen; Y Yang; Wu-Yen Hung; anser azim; Saeed Bohlega; Rup Tandan; C Warner; N G Laing; F Cambi; Hiroshi Mitsumoto; Raymond P Roos; Rose-Mary N Boustany; Mongi Ben Hamida; Faycal Hentati; Teepu Siddique
Novel mutations in spastin gene and absence of correlation with age at onset of symptoms.
Neurology 2000;55(9):1388-90.
2000: Adel Driss; Rim Amouri; Christiane Ben Hamida; S Souilem; Neziha Gouider-Khouja; Mongi Ben Hamida; Faycal Hentati
A new locus for autosomal recessive limb-girdle muscular dystrophy in a large consanguineous Tunisian family maps to chromosome 19q13.3.
Neuromuscular disorders : NMD 2000;10(4-5):240-6.
1999: R P Copp; Thomas Wisniewski; Faycal Hentati; Abdelmajid Larnaout; Mongi Ben Hamida; HJ Kayden
Localization of alpha-tocopherol transfer protein in the brains of patients with ataxia with vitamin E deficiency and other oxidative stress related neurodegenerative disorders.
Brain research 1999;822(1-2):80-7.
1999: Neziha Gouider-Khouja; Ilhem Turki; Mongi Ben Hamida; Faycal Hentati
[Treatment of cervical dystonia with botulinum toxin].
La Tunisie médicale 1999;77(2):101-4.
1999: Neziha Gouider-Khouja; Ilhem Turki; Mongi Ben Hamida; Faycal Hentati
[Hemifacial spasm and its treatment with botulinum toxin].
La Tunisie médicale 1999;77(1):41-4.
1998: A Hentati; Karim Ouahchi; Margaret Pericak-Vance; D Nijhawan; A Ahmad; Y Yang; Jacqueline B Rimmler; W Hung; B Schlotter; A Ahmed; Mongi Ben Hamida; Faycal Hentati; Teepu Siddique
Linkage of a commoner form of recessive amyotrophic lateral sclerosis to chromosome 15q15-q22 markers.
Neurogenetics 1998;2(1):55-60.
1998: K Ben Othmane; Julie M Rochelle; Mongi Ben Hamida; BD Slotterbeck; N Rao; Faycal Hentati; Margaret Pericak-Vance; Jeffery Vance
Fine localization of the CMT4A locus using a PAC contig and haplotype analysis.
Neurogenetics 1998;2(1):18-23.
1998: Abdelmajid Larnaout; Mongi Ben Hamida; Faycal Hentati
A clinicopathological observation of Nyssen-van Bogaert syndrome with second motor neuron degeneration: two distinct clinical entities.
Acta neurologica Scandinavica 1998;98(6):452-7.
1998: Abdelmajid Larnaout; MA Mongalgi; Neziha Kaabachi; D Khiari; Ali Debbabi; A Mebazza; Mongi Ben Hamida; Faycal Hentati
Methylmalonic acidaemia with bilateral globus pallidus involvement: a neuropathological study.
Journal of inherited metabolic disease 1998;21(6):639-44.
1998: Mourad Zouari; Moncef Feki; Christiane Ben Hamida; Abdelmajid Larnaout; Ilhem Turki; Samir Belal; Abderraouf Mebazaa; Mongi Ben Hamida; Faycal Hentati
Electrophysiology and nerve biopsy: comparative study in Friedreich's ataxia and Friedreich's ataxia phenotype with vitamin E deficiency.
Neuromuscular disorders : NMD 1998;8(6):416-25.
1998: Abdelmajid Larnaout; Samir Belal; Christiane Ben Hamida; Mongi Ben Hamida; Faycal Hentati
Atypical ataxia telangiectasia with early childhood lower motor neuron degeneration: a clinicopathological observation in three siblings.
Journal of neurology 1998;245(4):231-5.
1998: J Liu; C Wu; K Bossie; Khemissa Bejaoui; Betsy A Hosler; J C Gingrich; Mongi Ben Hamida; Faycal Hentati; E Schurr; P J de Jong; Robert H Brown
Generation of a 3-Mb PAC contig spanning the Miyoshi myopathy/limb-girdle muscular dystrophy (MM/LGMD2B) locus on chromosome 2p13.
Genomics 1998;49(1):23-9.
1997: Christiane Ben Hamida; L Cavalier; Samir Belal; H Sanhaji; N Nadal; C Barhoumi; N M'Rissa; MARZOUKI NAIMA; J L Mandel; Mongi Ben Hamida; Michel Koenig; Faycal Hentati
Homozygosity mapping of giant axonal neuropathy gene to chromosome 16q24.1.
Neurogenetics 1997;1(2):129-33.
1997: Abdelmajid Larnaout; Samir Belal; Mourad Zouari; M Fki; Christiane Ben Hamida; H H Goebel; Mongi Ben Hamida; Faycal Hentati
Friedreich's ataxia with isolated vitamin E deficiency: a neuropathological study of a Tunisian patient.
Acta neuropathologica 1997;93(6):633-7.
1996: Mongi Ben Hamida; Christiane Ben Hamida; Mourad Zouari; Samir Belal; Faycal Hentati
Limb-girdle muscular dystrophy 2C: clinical aspects.
Neuromuscular disorders : NMD 1996;6(6):493-4.
1995: Satoru Noguchi; Elizabeth McNally; K Ben Othmane; Y Hagiwara; Y Mizuno; Mikiharu Yoshida; H Yamamoto; Carsten G Bönnemann; Emanuela Gussoni; P H Denton; T Kyriakides; Lefkos T Middleton; Faycal Hentati; Mongi Ben Hamida; I Nonaka; Jeffery Vance; Louis Kunkel; Eijiro Ozawa
Mutations in the dystrophin-associated protein gamma-sarcoglycan in chromosome 13 muscular dystrophy.
Science (New York, N.Y.) 1995;270(5237):819-22.
1995: K B Othmane; D Loeb; R Hayworth-Hodgte; Faycal Hentati; N Rao; Allen D Roses; Mongi Ben Hamida; Margaret Pericak-Vance; Jeffery Vance
Physical and genetic mapping of the CMT4A locus and exclusion of PMP-2 as the defect in CMT4A.
Genomics 1995;28(2):286-90.
1995: Mongi Ben Hamida; K Ben Othmane; S Belal; Faycal Hentati
[Is there a single form of Charcot-Marie-Tooth disease, or are there several variations? A classification difficulty].
Revue neurologique 1995;151(4):221-4.
1995: Samir Belal; Faycal Hentati; Christiane Ben Hamida; Mongi Ben Hamida
Friedreich's ataxia-vitamin E responsive type. The chromosome 8 locus.
Clinical neuroscience (New York, N.Y.) 1995;3(1):39-42.
1994: Kamel Hamzaoui; Agnes Hamzaoui; Faycal Hentati; A Kahan; Khaled Ayed; A Chabbou; Mongi Ben Hamida; M Hamza
Phenotype and functional profile of T cells expressing gamma delta receptor from patients with active Behçet's disease.
The Journal of rheumatology 1994;21(12):2301-6.
1994: Abdelmajid Larnaout; Faycal Hentati; Christiane Ben Hamida; N Khrouf; Mongi Ben Hamida
[Congenital fibrolipoma of the mesencephalic protuberation area].
Archives de pédiatrie : organe officiel de la Sociéte française de pédiatrie 1994;1(10):913-5.
1994: Kamel Hamzaoui; Faycal Hentati; Agnes Hamzaoui; A Kahan; Mongi Ben Hamida; A Chabbou; Khaled Ayed
CD11/CD18 bearing lymphocytes in cerebrospinal fluid from patients with active Behçet's disease.
Clinical and experimental rheumatology 1994;12(5):575-6.
1994: Samir Belal; G Cancel; Giovanni Stevanin; Faycal Hentati; C Khati; Christiane Ben Hamida; Georg Auburger; Yves Agid; Mongi Ben Hamida; Alexis Brice
Clinical and genetic analysis of a Tunisian family with autosomal dominant cerebellar ataxia type 1 linked to the SCA2 locus.
Neurology 1994;44(8):1423-6.
1994: Abdelmajid Larnaout; Faycal Hentati; Samir Belal; Christiane Ben Hamida; Neziha Kaabachi; Mongi Ben Hamida
Clinical and pathological study of three Tunisian siblings with L-2-hydroxyglutaric aciduria.
Acta neuropathologica 1994;88(4):367-70.
1993: N Attia-Romdhane; Amel Mrabet; Mongi Ben Hamida
Prevalence of epilepsy in Kelibia, Tunisia.
Epilepsia 1993;34(6):1028-32.
1993: Mongi Ben Hamida; Samir Belal; Giorgio Sirugo; Christiane Ben Hamida; Kyproula Christodoulou; P Ionannou; Jacques Beckmann; Jean-Louis Mandel; Faycal Hentati; Michel Koenig
Friedreich's ataxia phenotype not linked to chromosome 9 and associated with selective autosomal recessive vitamin E deficiency in two inbred Tunisian families.
Neurology 1993;43(11):2179-83.
1993: K Ben Othmane; Faycal Hentati; F Lennon; Christiane Ben Hamida; S Blel; Allen D Roses; Margaret Pericak-Vance; Mongi Ben Hamida; Jeffery Vance
Linkage of a locus (CMT4A) for autosomal recessive Charcot-Marie-Tooth disease to chromosome 8q.
Human molecular genetics 1993;2(10):1625-8.
1993: Mongi Ben Hamida; N Attia-Romdhane; Faycal Hentati; C Triki
Early onset ataxias in Tunisia. Intrafamilial heterogeneity.
Advances in neurology 1993;61():105-14.
1993: N Attia Romdhane; Mongi Ben Hamida; Amel Mrabet; Abdelmajid Larnaout; S Samoud; A Ben Hamda; M Ben Hamda; S Oueslati
Prevalence study of neurologic disorders in Kelibia (Tunisia).
Neuroepidemiology 1993;12(5):285-99.
1993: Neziha Kaabachi; Abdelmajid Larnaout; D Rabier; C Jakobs; Samir Belal; Faycal Hentati; P Parvey; J Bardet; Mongi Ben Hamida; Abderraouf Mebazaa
Familial encephalopathy and L-2-hydroxyglutaric aciduria.
Journal of inherited metabolic disease 1993;16(5):893.
1992: Samir Belal; Kyproula Christodoulou; Giorgio Sirugo; Christiane Ben Hamida; P Ioannou; Faycal Hentati; Jacques Beckmann; Michel Koenig; Jean-Louis Mandel; Mongi Ben Hamida
Study of large inbred Friedreich ataxia families reveals a recombination between D9S15 and the disease locus.
American journal of human genetics 1992;51(6):1372-6.
1992: Abdelmajid Larnaout; MA Mongalgi; H Ben Ameur; Faycal Hentati; Ali Debbabi; Mongi Ben Hamida
[Antenatal bilateral sylvian infarction and congenital syphilis].
Archives françaises de pédiatrie 1992;49(10):895-7.
1992: K Ben Othmane; Mongi Ben Hamida; Margaret Pericak-Vance; Christiane Ben Hamida; S Blel; S C Carter; A M Bowcock; K Petruhkin; T C Gilliam; Allen D Roses
Linkage of Tunisian autosomal recessive Duchenne-like muscular dystrophy to the pericentromeric region of chromosome 13q.
Nature genetics 1992;2(4):315-7.
1992: Mongi Ben Hamida; Nakjoua Miladi; Ilhem Turki; H Zaiem
Duchenne muscular dystrophy in Tunisia: a clinical and morphological study of 77 cases.
Journal of the neurological sciences 1992;107(1):60-4.
1992: Nakjoua Miladi; Abdelmajid Larnaout; Neziha Kaabachi; M Helayem; Mongi Ben Hamida
Phenylketonuria: an underlying etiology of autistic syndrome. A case report.
Journal of child neurology 1992;7(1):22-3.
1992: Abdelmajid Larnaout; M Haddad; Faycal Hentati; Mongi Ben Hamida
[Candida albicans meningitis and neurosarcoidosis].
Revue neurologique 1992;148(12):762-6.
1992: Faycal Hentati; Christiane Ben Hamida; M Zeghal; M Kamoun; B Fezaa; Mongi Ben Hamida
Age-dependent axonal loss in nerve biopsy of patients with xeroderma pigmentosum.
Neuromuscular disorders : NMD 1992;2(5-6):361-9.
1991: Mongi Ben Hamida; Nakjoua Miladi; C Ben Hamida
[Schwartz-Jampel syndrome. Clinical and histopathological study of 4 cases].
Revue neurologique 1991;147(4):279-84.
1991: Amel Mrabet; S Oueslati; H Gazzah; Mongi Ben Hamida
[Clinical and electrophysiological study of 2 familial cases of Marcus Gunn phenomenon].
Revue neurologique 1991;147(3):215-9.
1991: Mongi Ben Hamida; N Attia-Romdhane; C H Triki; S Oueslati; Faycal Hentati
[Clinical and genetic analysis of 188 families with spinocerebellar degeneration. Friedreich's disease and P. Marie's hereditary ataxias].
Revue neurologique 1991;147(12):798-808.
1991: Mongi Ben Hamida; N Chabbi; Christiane Ben Hamida; C Mhiri; R Kallel
[Peripheral neuropathy in a sporadic case of cerebrotendinous xanthomatosis].
Revue neurologique 1991;147(5):385-8.
1990: Mongi Ben Hamida; Faycal Hentati; Christiane Ben Hamida
Hereditary motor system diseases (chronic juvenile amyotrophic lateral sclerosis). Conditions combining a bilateral pyramidal syndrome with limb and bulbar amyotrophy.
Brain : a journal of neurology 1990;113 ( Pt 2)():347-63.
1990: N Gharbi; Amel Mrabet; Mongi Ben Hamida
[Analysis of cerebro-spinal fluid proteins in neurologic and serologic syphilis].
La Tunisie médicale 1990;68(3):205-8.
1990: Amel Mrabet; N Attia-Romdhane; Mongi Ben Hamida; N Gharbi; H Le Noan; R Hentati; J Ben Mansour; I Srairi
[Epidemiologic aspects of cerebrovascular accidents in Tunisia].
Revue neurologique 1990;146(4):297-301.
1990: Mongi Ben Hamida; N Chabbi
[Opto-chiasmatic tuberculoma disclosed by unilateral exophthalmos. Clinico-pathologic study].
Revue neurologique 1990;146(3):211-3.
1989: Amel Mrabet; N Gharbi; N Attia-Romdhane; H Le Noan; Mongi Ben Hamida
[Brain-type creatine kinase isoenzymes (CK BB) in cerebrovascular accidents].
La Tunisie médicale 1989;67(6-7):397-400.
1989: Amel Mrabet; M Jellouli; S Touibi; Mongi Ben Hamida
[2 cases of vascular syndrome of the cranial nerves of ischemic origin].
Annales de médecine interne 1989;140(1):14-8.
1988: Mongi Ben Hamida; Faycal Hentati; N Chebbi; C Mhiri; Khaled Ayed; Kamel Hamzaoui
[Chronic proximal spinal amyotrophies in Tunisia. Clinical, genetic, epidemiologic and histopathologic study].
Revue neurologique 1988;144(11):737-47.
1987: S Madani; J Baillon; J Fries; O Belhadj; A Bettaieb; Mongi Ben Hamida; Guy Hervé
Pyrimidine pathways enzymes in human tumors of brain and associated tissues: potentialities for the therapeutic use of N-(phosphonacetyl-L-aspartate and 1-beta-D-arabinofuranosylcytosine.
European journal of cancer & clinical oncology 1987;23(10):1485-90.
1987: Mongi Ben Hamida; F Letaief; Faycal Hentati; Christiane Ben Hamida
Morphometric study of the sensory nerve in classical (or Charcot disease) and juvenile amyotrophic lateral sclerosis.
Journal of the neurological sciences 1987;78(3):313-29.
1987: Mongi Ben Hamida; F Letaief; Christiane Ben Hamida
Histomorphometric study of the superficial peroneal nerve in leprosy.
Acta leprologica 1987;5(2):101-14.
1987: Mongi Ben Hamida; F Letaief; Faycal Hentati; Christiane Ben Hamida
Hypertrophic neuropathy in spinocerebellar degeneration. Morphological study of the superficial peroneal nerve in fourteen cases.
Acta neuropathologica 1987;75(1):51-61.
1987: F Zouiten; F Letaief; M Hamza; N Tougorti; C Kooli; Mongi Ben Hamida; Mohamed Miled
[Polymyositis with polyradiculoneuritis].
La Tunisie médicale 1987;65(1):57-60.
1986: Mongi Ben Hamida; H Chaabouni; S Madani; S Boussen; S Samoud; F Letaief; Amel Mrabet; Faycal Hentati; Nakjoua Miladi
[Genetic study of spinocerebellar hereditary degenerations in Tunisia. Role of consanguinity in their occurrence].
Journal de génétique humaine 1986;34(3-4):267-74.
1986: Mongi Ben Hamida; Faycal Hentati; Christiane Ben Hamida; N Slimane; T Ben Othman; N Chebbi; F Letaief
[Case of the rigid spine syndrome in a female patient].
La Tunisie médicale 1986;64(6-7):645-8.
1985: Mongi Ben Hamida; N Attia-Romdhane; A Mrabet-Bahri; A Ben Hamda; M Slim; Abdelmajid Larnaout
[The motor handicapped].
La Tunisie médicale 1985;63(4):251-88.
1984: I Chami; Nakjoua Miladi; Mongi Ben Hamida; S Zmerli
[Continence disorders in hereditary spinocerebellar degeneration. Comparison of clinical and urodynamic findings in 55 cases].
Acta neurologica Belgica 1984;84(4):194-203.
1982: Mongi Ben Hamida; Amel Mrabet; S Samoud
[Neurologic manifestations of Behçet's disease. Apropos of 27 cases].
La Tunisie médicale 1982;60(2):112-6.
1982: Mongi Ben Hamida; M Marzouki
[Status epilepticus: triggering factors and prognosis. Apropos of 37 cases].
La Tunisie médicale 1982;60(1):17-20.
1981: Mongi Ben Hamida; F Letaief; Christiane Ben Hamida; S Samoud
[Peroneal atrophy in Tunisia. Study of 70 cases, pure or associated with other heredodegenerative diseases].
Journal of the neurological sciences 1981;50(3):335-56.
1980: Mongi Ben Hamida; S Madani; S Zmerli; I Chami; A Annabi; M Jamoussi; M Marzouki; M Rachdi; S Samoud; M Talbi
[Hereditary degenerative spinocerebellar diseases in Tunisia with manometric studies in bladder disorders (author's transl)].
Revue neurologique 1980;136(8-9):495-508.