Ben Hamida M - Search Results

1

Limb-girdle muscular dystrophy 2C: clinical aspects.

Ben Hamida M, Ben Hamida C, Zouari M, Belal S, Hentati F. Ben Hamida M, et al. Among authors: ben hamida c. Neuromuscul Disord. 1996 Dec;6(6):493-4. doi: 10.1016/s0960-8966(96)00395-1. Neuromuscul Disord. 1996. PMID: 9027861

2

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

3

Electrophysiology and nerve biopsy: comparative study in Friedreich's ataxia and Friedreich's ataxia phenotype with vitamin E deficiency.

Zouari M, Feki M, Ben Hamida C, Larnaout A, Turki I, Belal S, Mebazaa A, Ben Hamida M, Hentati F. Zouari M, et al. Among authors: ben hamida m, ben hamida c. Neuromuscul Disord. 1998 Aug;8(6):416-25. doi: 10.1016/s0960-8966(98)00051-0. Neuromuscul Disord. 1998. PMID: 9713861

4

A new locus for autosomal recessive limb-girdle muscular dystrophy in a large consanguineous Tunisian family maps to chromosome 19q13.3.

Driss A, Amouri R, Ben Hamida C, Souilem S, Gouider-Khouja N, Ben Hamida M, Hentati F. Driss A, et al. Among authors: ben hamida m, ben hamida c. Neuromuscul Disord. 2000 Jun;10(4-5):240-6. doi: 10.1016/s0960-8966(00)00099-7. Neuromuscul Disord. 2000. PMID: 10838249

5

Linkage of a new locus for autosomal recessive axonal form of Charcot-Marie-Tooth disease to chromosome 8q21.3.

Barhoumi C, Amouri R, Ben Hamida C, Ben Hamida M, Machghoul S, Gueddiche M, Hentati F. Barhoumi C, et al. Among authors: ben hamida m, ben hamida c. Neuromuscul Disord. 2001 Jan;11(1):27-34. doi: 10.1016/s0960-8966(00)00162-0. Neuromuscul Disord. 2001. PMID: 11166163

6

Phenotype and sarcoglycan expression in Tunisian LGMD 2C patients sharing the same del521-T mutation.

Kefi M, Amouri R, Driss A, Ben Hamida C, Ben Hamida M, Kunkel LM, Hentati F. Kefi M, et al. Among authors: ben hamida m, ben hamida c. Neuromuscul Disord. 2003 Dec;13(10):779-87. doi: 10.1016/s0960-8966(03)00136-6. Neuromuscul Disord. 2003. PMID: 14678800

7

Age-dependent axonal loss in nerve biopsy of patients with xeroderma pigmentosum.

Hentati F, Ben Hamida C, Zeghal M, Kamoun M, Fezaa B, Ben Hamida M. Hentati F, et al. Among authors: ben hamida m, ben hamida c. Neuromuscul Disord. 1992;2(5-6):361-9. doi: 10.1016/s0960-8966(06)80007-6. Neuromuscul Disord. 1992. PMID: 1300184

8

Expression of myosin isoforms and of desmin, vimentin and titin in Tunisian Duchenne-like autosomal recessive muscular dystrophy.

Hamida CB, Soussi-Yanicostas N, Bejaoui K, Butler-Browne GS, Hentati F, Ben Hamida M. Hamida CB, et al. Among authors: ben hamida m. J Neurol Sci. 1994 May;123(1-2):114-21. doi: 10.1016/0022-510x(94)90212-7. J Neurol Sci. 1994. PMID: 8064303

9

Autosomal recessive parkinsonism linked to parkin gene in a Tunisian family. Clinical, genetic and pathological study.

Gouider-Khouja N, Larnaout A, Amouri R, Sfar S, Belal S, Ben Hamida C, Ben Hamida M, Hattori N, Mizuno Y, Hentati F. Gouider-Khouja N, et al. Among authors: ben hamida m, ben hamida c. Parkinsonism Relat Disord. 2003 Jun;9(5):247-51. doi: 10.1016/s1353-8020(03)00016-6. Parkinsonism Relat Disord. 2003. PMID: 12781588

10

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

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