Ben Hamida M - Search Results

1

Early onset ataxias in Tunisia. Intrafamilial heterogeneity.

Ben Hamida M, Attia-Romdhane N, Hentati F, Triki C. Ben Hamida M, et al. Adv Neurol. 1993;61:105-14. Adv Neurol. 1993. PMID: 8421961 Review. No abstract available.

2

Clinical and genetic analysis of a Tunisian family with autosomal dominant cerebellar ataxia type 1 linked to the SCA2 locus.

Belal S, Cancel G, Stevanin G, Hentati F, Khati C, Ben Hamida C, Auburger G, Agid Y, Ben Hamida M, Brice A. Belal S, et al. Among authors: ben hamida m, ben hamida c. Neurology. 1994 Aug;44(8):1423-6. doi: 10.1212/wnl.44.8.1423. Neurology. 1994. PMID: 8058142

3

Atypical amyotrophic lateral sclerosis.

Ben Hamida M, Hentati F. Ben Hamida M, et al. Adv Neurol. 1995;68:153-5. Adv Neurol. 1995. PMID: 8787225 Review. No abstract available.

4

[Clinical and genetic analysis of 188 families with spinocerebellar degeneration. Friedreich's disease and P. Marie's hereditary ataxias].

Ben Hamida M, Attia-Romdhane N, Triki CH, Oueslati S, Hentati F. Ben Hamida M, et al. Rev Neurol (Paris). 1991;147(12):798-808. Rev Neurol (Paris). 1991. PMID: 1780608 French.

5

Juvenile amyotrophic lateral sclerosis and related syndromes.

Ben Hamida M, Hentati F. Ben Hamida M, et al. Adv Neurol. 1991;56:175-9. Adv Neurol. 1991. PMID: 1853755 No abstract available.

6

Clinical and pathological study of three Tunisian siblings with L-2-hydroxyglutaric aciduria.

Larnaout A, Hentati F, Belal S, Ben Hamida C, Kaabachi N, Ben Hamida M. Larnaout A, et al. Among authors: ben hamida m, ben hamida c. Acta Neuropathol. 1994;88(4):367-70. doi: 10.1007/BF00310381. Acta Neuropathol. 1994. PMID: 7839830

7

Friedreich's ataxia phenotype not linked to chromosome 9 and associated with selective autosomal recessive vitamin E deficiency in two inbred Tunisian families.

Ben Hamida M, Belal S, Sirugo G, Ben Hamida C, Panayides K, Ionannou P, Beckmann J, Mandel JL, Hentati F, Koenig M, et al. Ben Hamida M, et al. Among authors: ben hamida c. Neurology. 1993 Nov;43(11):2179-83. doi: 10.1212/wnl.43.11.2179. Neurology. 1993. PMID: 8232925

8

Prevalence of epilepsy in Kelibia, Tunisia.

Attia-Romdhane N, Mrabet A, Ben Hamida M. Attia-Romdhane N, et al. Among authors: ben hamida m. Epilepsia. 1993 Nov-Dec;34(6):1028-32. doi: 10.1111/j.1528-1157.1993.tb02129.x. Epilepsia. 1993. PMID: 8243352

9

Prevalence study of neurologic disorders in Kelibia (Tunisia).

Attia Romdhane N, Ben Hamida M, Mrabet A, Larnaout A, Samoud S, Ben Hamda A, Ben Hamda M, Oueslati S. Attia Romdhane N, et al. Among authors: ben hamida m, ben hamda m, ben hamda a. Neuroepidemiology. 1993;12(5):285-99. doi: 10.1159/000110330. Neuroepidemiology. 1993. PMID: 8309504

10

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

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