Ben Hamida C - Search Results

1

The gene encoding gigaxonin, a new member of the cytoskeletal BTB/kelch repeat family, is mutated in giant axonal neuropathy.

Bomont P, Cavalier L, Blondeau F, Ben Hamida C, Belal S, Tazir M, Demir E, Topaloglu H, Korinthenberg R, Tüysüz B, Landrieu P, Hentati F, Koenig M. Bomont P, et al. Among authors: ben hamida c. Nat Genet. 2000 Nov;26(3):370-4. doi: 10.1038/81701. Nat Genet. 2000. PMID: 11062483

2

Giant axonal neuropathy locus refinement to a < 590 kb critical interval.

Cavalier L, BenHamida C, Amouri R, Belal S, Bomont P, Lagarde N, Gressin L, Callen D, Demir E, Topaloglu H, Landrieu P, Ioos C, Hamida MB, Koenig M, Hentati F. Cavalier L, et al. Eur J Hum Genet. 2000 Jul;8(7):527-34. doi: 10.1038/sj.ejhg.5200476. Eur J Hum Genet. 2000. PMID: 10909853

3

Giant axonal neuropathy with inherited multisystem degeneration in a Tunisian kindred.

Ben Hamida M, Hentati F, Ben Hamida C. Ben Hamida M, et al. Among authors: ben hamida c. Neurology. 1990 Feb;40(2):245-50. doi: 10.1212/wnl.40.2.245. Neurology. 1990. PMID: 2153943

4

Ataxia with vitamin E deficiency: refinement of genetic localization and analysis of linkage disequilibrium by using new markers in 14 families.

Doerflinger N, Linder C, Ouahchi K, Gyapay G, Weissenbach J, Le Paslier D, Rigault P, Belal S, Ben Hamida C, Hentati F, et al. Doerflinger N, et al. Among authors: ben hamida c. Am J Hum Genet. 1995 May;56(5):1116-24. Am J Hum Genet. 1995. PMID: 7726167 Free PMC article.

5

Homozygosity mapping of giant axonal neuropathy gene to chromosome 16q24.1.

Ben Hamida C, Cavalier L, Belal S, Sanhaji H, Nadal N, Barhoumi C, M'Rissa N, Marzouki N, Mandel JL, Ben Hamida M, Koenig M, Hentati F. Ben Hamida C, et al. Among authors: ben hamida m. Neurogenetics. 1997 Sep;1(2):129-33. doi: 10.1007/s100480050019. Neurogenetics. 1997. PMID: 10732815

6

Study of large inbred Friedreich ataxia families reveals a recombination between D9S15 and the disease locus.

Belal S, Panayides K, Sirugo G, Ben Hamida C, Ioannou P, Hentati F, Beckmann J, Koenig M, Mandel JL, Ben Hamida M, et al. Belal S, et al. Among authors: ben hamida m, ben hamida c. Am J Hum Genet. 1992 Dec;51(6):1372-6. Am J Hum Genet. 1992. PMID: 1463017 Free PMC article.

7

Genetic analysis of early onset cerebellar ataxia with retained tendon reflexes in four Tunisian families.

Marzouki N, Belal S, Benhamida C, Benlemlih M, Hentati F. Marzouki N, et al. Clin Genet. 2001 Apr;59(4):257-62. doi: 10.1034/j.1399-0004.2001.590407.x. Clin Genet. 2001. PMID: 11298681

8

Atypical ataxia telangiectasia with early childhood lower motor neuron degeneration: a clinicopathological observation in three siblings.

Larnaout A, Belal S, Ben Hamida C, Ben Hamida M, Hentati F. Larnaout A, et al. Among authors: ben hamida m, ben hamida c. J Neurol. 1998 Apr;245(4):231-5. doi: 10.1007/s004150050210. J Neurol. 1998. PMID: 9591225

9

Friedreich's ataxia-vitamin E responsive type. The chromosome 8 locus.

Belal S, Hentati F, Ben Hamida C, Ben Hamida M. Belal S, et al. Among authors: ben hamida m, ben hamida c. Clin Neurosci. 1995;3(1):39-42. Clin Neurosci. 1995. PMID: 7614093

10

Localization of Friedreich ataxia phenotype with selective vitamin E deficiency to chromosome 8q by homozygosity mapping.

Ben Hamida C, Doerflinger N, Belal S, Linder C, Reutenauer L, Dib C, Gyapay G, Vignal A, Le Paslier D, Cohen D, et al. Ben Hamida C, et al. Nat Genet. 1993 Oct;5(2):195-200. doi: 10.1038/ng1093-195. Nat Genet. 1993. PMID: 8252047

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