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Results: 1-11 |
Results: 11
Effect of vitamin E supplementation in patients with ataxia with vitamin Edeficiency
Authors: Gabsi, S Gouider-Khouja, N Belal, S Fki, M Kefi, M Turki, I Ben Hamida, M Kayden, H Mebazaa, R Hentati, F
Citation: S. Gabsi et al., Effect of vitamin E supplementation in patients with ataxia with vitamin Edeficiency, EUR J NEUR, 8(5), 2001, pp. 477-481
Linkage of a new locus for autosomal recessive axonal form of Charcot-Marie-Tooth disease to chromosome 8q21.3
Authors: Barhoumi, C Amouri, R Ben Hamida, C Ben Hamida, M Machghoul, S Gueddiche, M Hentati, F
Citation: C. Barhoumi et al., Linkage of a new locus for autosomal recessive axonal form of Charcot-Marie-Tooth disease to chromosome 8q21.3, NEUROMUSC D, 11(1), 2001, pp. 27-34
Wernicke's encephalopathy in a patient with Crohn's disease: a pathological study
Authors: Larnaout, A El-Euch, G Kchir, N Filali, A Ben Hamida, M Hentati, F
Citation: A. Larnaout et al., Wernicke's encephalopathy in a patient with Crohn's disease: a pathological study, J NEUROL, 248(1), 2001, pp. 57-60
Giant axonal neuropathy locus refinement to a < 590 kb critical interval
Authors: Cavalier, L BenHamida, C Amouri, R Belal, S Bomont, P Lagarde, N Gressin, L Callen, D Demir, E Topaloglu, H Landrieu, P Ioos, C Ben Hamida, M Koenig, M Hentati, F
Citation: L. Cavalier et al., Giant axonal neuropathy locus refinement to a < 590 kb critical interval, EUR J HUM G, 8(7), 2000, pp. 527-534
A new locus for autosomal recessive limb-girdle muscular dystrophy in a large consanguineous Tunisian family maps to chromosome 19q13.3
Authors: Driss, A Amouri, R Ben Hamida, C Souilem, S Gouider-Khouja, N Ben Hamida, M Hentati, F
Citation: A. Driss et al., A new locus for autosomal recessive limb-girdle muscular dystrophy in a large consanguineous Tunisian family maps to chromosome 19q13.3, NEUROMUSC D, 10(4-5), 2000, pp. 240-246
Novel mutations in spastin gene and absence of correlation with age at onset of symptoms
Authors: Hentati, A Deng, HX Zhai, H Chen, W Yang, Y Hung, WY Azim, AC Bohlega, S Tandan, R Warner, C Laing, NG Cambi, F Mitsumoto, H Roos, RP Boustany, RM Ben Hamida, M Hentati, F Siddique, T
Citation: A. Hentati et al., Novel mutations in spastin gene and absence of correlation with age at onset of symptoms, NEUROLOGY, 55(9), 2000, pp. 1388-1390
Clinical and genetic study of familial Parkinson's disease in Tunisia
Authors: Gouider-Khouja, N Belal, S Ben Hamida, M Hentati, F
Citation: N. Gouider-khouja et al., Clinical and genetic study of familial Parkinson's disease in Tunisia, NEUROLOGY, 54(8), 2000, pp. 1603-1609
Linkage to chromosome 13q11-12 of an autosomal recessive cerebellar ataxiain a Tunisian family
Authors: Mrissa, N Belal, S Ben Hamida, C Amouri, R Turki, I Mrissa, R Ben Hamida, M Hentati, F
Citation: N. Mrissa et al., Linkage to chromosome 13q11-12 of an autosomal recessive cerebellar ataxiain a Tunisian family, NEUROLOGY, 54(7), 2000, pp. 1408-1414
Identification of a new locus for autosomal recessive Charcot-Marie-Tooth disease with focally folded myelin on chromosome 11p15
Authors: Ben Othmane, K Johnson, E Menold, M Graham, FL Ben Hamida, M Hasegawa, O Rogala, AD Ohnishi, A Pericak-Vance, M Hentati, F Vance, JM
Citation: K. Ben Othmane et al., Identification of a new locus for autosomal recessive Charcot-Marie-Tooth disease with focally folded myelin on chromosome 11p15, GENOMICS, 62(3), 1999, pp. 344-349
Localization of alpha-tocopherol transfer protein in the brains of patients with ataxia with vitamin E deficiency and other oxidative stress related neurodegenerative disorders
Authors: Copp, RP Wisniewski, T Hentati, F Larnaout, A Ben Hamida, M Kayden, HJ
Citation: Rp. Copp et al., 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 RES, 822(1-2), 1999, pp. 80-87
A clinicopathological observation of Nyssen-van Bogaert syndrome with second motor neuron degeneration: two distinct clinical entities
Authors: Larnaout, A Ben Hamida, M Hentati, F
Citation: A. Larnaout et al., A clinicopathological observation of Nyssen-van Bogaert syndrome with second motor neuron degeneration: two distinct clinical entities, ACT NEUR SC, 98(6), 1998, pp. 452-457
Risultati: 1-11 |