Ben Hamida M - Search Results

1

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.

2

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.

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

[Juvenile amyotrophic lateral sclerosis. Study of 43 cases].

Ben Hamida M, Hentati F, Ben Hamida C. Ben Hamida M, et al. Among authors: ben hamida c. Bull Acad Natl Med. 1992 Feb;176(2):213-9; discussion 219-22. Bull Acad Natl Med. 1992. PMID: 1633561 French.

5

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: ben hamida c. Brain. 1990 Apr;113 ( Pt 2):347-63. doi: 10.1093/brain/113.2.347. Brain. 1990. PMID: 2328408

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

7

[Charcot's disease and juvenile amyotrophic lateral sclerosis].

Ben Hamida M, Hentati F. Ben Hamida M, et al. Rev Neurol (Paris). 1984;140(3):202-6. Rev Neurol (Paris). 1984. PMID: 6729330 French.

8

[Congenital fibrolipoma of the mesencephalic protuberation area].

Larnaout A, Hentati F, Ben Hamida C, Khrouf N, Ben Hamida M. Larnaout A, et al. Among authors: ben hamida m, ben hamida c. Arch Pediatr. 1994 Oct;1(10):913-5. Arch Pediatr. 1994. PMID: 7842073 French.

9

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

10

Biochemical and immunocytochemical analysis in chronic proximal spinal muscular atrophy.

Ben Hamida C, Soussi-Yanicostas N, Butler-Browne GS, Bejaoui K, Hentati F, Ben Hamida M. Ben Hamida C, et al. Among authors: ben hamida m. Muscle Nerve. 1994 Apr;17(4):400-10. doi: 10.1002/mus.880170407. Muscle Nerve. 1994. PMID: 8170486

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

131 results

Search Page

Filters