Hentati F - 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. Among authors: hentati f. Adv Neurol. 1993;61:105-14. Adv Neurol. 1993. PMID: 8421961 Review. No abstract available.

2

[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. Among authors: hentati f. Rev Neurol (Paris). 1991;147(12):798-808. Rev Neurol (Paris). 1991. PMID: 1780608 French.

3

Juvenile amyotrophic lateral sclerosis and related syndromes.

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

4

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: hentati f. Neurology. 1994 Aug;44(8):1423-6. doi: 10.1212/wnl.44.8.1423. Neurology. 1994. PMID: 8058142

5

Atypical amyotrophic lateral sclerosis.

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

6

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: hentati f. Neurology. 1990 Feb;40(2):245-50. doi: 10.1212/wnl.40.2.245. Neurology. 1990. PMID: 2153943

7

Presence of normal dystrophin in Tunisian severe childhood autosomal recessive muscular dystrophy.

Ben Jelloun-Dellagi S, Chaffey P, Hentati F, Ben Hamida C, Tome F, Colin H, Dellagi K, Kaplan JC, Fardeau M, Ben Hamida M. Ben Jelloun-Dellagi S, et al. Among authors: hentati f. Neurology. 1990 Dec;40(12):1903. doi: 10.1212/wnl.40.12.1903. Neurology. 1990. PMID: 2247244 No abstract available.

8

Hereditary motor system diseases (chronic juvenile amyotrophic lateral sclerosis). Conditions combining a bilateral pyramidal syndrome with limb and bulbar amyotrophy.

Ben Hamida M, Hentati F, Ben Hamida C. Ben Hamida M, et al. Among authors: hentati f. Brain. 1990 Apr;113 ( Pt 2):347-63. doi: 10.1093/brain/113.2.347. Brain. 1990. PMID: 2328408

9

[Chronic proximal spinal amyotrophies in Tunisia. Clinical, genetic, epidemiologic and histopathologic study].

Ben Hamida M, Hentati F, Chebbi N, Mhiri C, Ayed K, Hamzaoui K. Ben Hamida M, et al. Among authors: hentati f. Rev Neurol (Paris). 1988;144(11):737-47. Rev Neurol (Paris). 1988. PMID: 3231963 French.

10

Hypertrophic neuropathy in spinocerebellar degeneration. Morphological study of the superficial peroneal nerve in fourteen cases.

Ben Hamida M, Letaief F, Hentati F, Ben Hamida C. Ben Hamida M, et al. Among authors: hentati f. Acta Neuropathol. 1987;75(1):51-61. doi: 10.1007/BF00686793. Acta Neuropathol. 1987. PMID: 3481153

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