Belal S - 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: belal s. 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. 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: belal s. Neuromuscul Disord. 1998 Aug;8(6):416-25. doi: 10.1016/s0960-8966(98)00051-0. Neuromuscul Disord. 1998. PMID: 9713861

4

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: belal s. Parkinsonism Relat Disord. 2003 Jun;9(5):247-51. doi: 10.1016/s1353-8020(03)00016-6. Parkinsonism Relat Disord. 2003. PMID: 12781588

5

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. Am J Hum Genet. 1992 Dec;51(6):1372-6. Am J Hum Genet. 1992. PMID: 1463017 Free PMC article.

6

Linkage of Miyoshi myopathy (distal autosomal recessive muscular dystrophy) locus to chromosome 2p12-14.

Bejaoui K, Hirabayashi K, Hentati F, Haines JL, Ben Hamida C, Belal S, Miller RG, McKenna-Yasek D, Weissenbach J, Rowland LP, et al. Bejaoui K, et al. Among authors: belal s. Neurology. 1995 Apr;45(4):768-72. doi: 10.1212/wnl.45.4.768. Neurology. 1995. PMID: 7723968

7

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: belal s. Acta Neuropathol. 1994;88(4):367-70. doi: 10.1007/BF00310381. Acta Neuropathol. 1994. PMID: 7839830

8

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

9

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: belal s. Neurology. 1993 Nov;43(11):2179-83. doi: 10.1212/wnl.43.11.2179. Neurology. 1993. PMID: 8232925

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: belal s. J Neurol. 1998 Apr;245(4):231-5. doi: 10.1007/s004150050210. J Neurol. 1998. PMID: 9591225

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