Belal S - Search Results

1

Linkage of 'pure' autosomal recessive familial spastic paraplegia to chromosome 8 markers and evidence of genetic locus heterogeneity.

Hentati A, Pericak-Vance MA, Hung WY, Belal S, Laing N, Boustany RM, Hentati F, Ben Hamida M, Siddique T. Hentati A, et al. Among authors: belal s. Hum Mol Genet. 1994 Aug;3(8):1263-7. doi: 10.1093/hmg/3.8.1263. Hum Mol Genet. 1994. PMID: 7987300

2

Phenotypic features and genetic findings in sacsin-related autosomal recessive ataxia in Tunisia.

El Euch-Fayache G, Lalani I, Amouri R, Turki I, Ouahchi K, Hung WY, Belal S, Siddique T, Hentati F. El Euch-Fayache G, et al. Among authors: belal s. Arch Neurol. 2003 Jul;60(7):982-8. doi: 10.1001/archneur.60.7.982. Arch Neurol. 2003. PMID: 12873855

3

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.

4

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

5

Ataxia with vitamin E deficiency: refinement of genetic localization and analysis of linkage disequilibrium by using new markers in 14 families.

Doerflinger N, Linder C, Ouahchi K, Gyapay G, Weissenbach J, Le Paslier D, Rigault P, Belal S, Ben Hamida C, Hentati F, et al. Doerflinger N, et al. Among authors: belal s. Am J Hum Genet. 1995 May;56(5):1116-24. Am J Hum Genet. 1995. PMID: 7726167 Free PMC article.

6

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

7

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

8

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

9

Linkage to chromosome 13q11-12 of an autosomal recessive cerebellar ataxia in a Tunisian family.

Mrissa N, Belal S, Hamida CB, Amouri R, Turki I, Mrissa R, Hamida MB, Hentati F. Mrissa N, et al. Among authors: belal s. Neurology. 2000 Apr 11;54(7):1408-14. doi: 10.1212/wnl.54.7.1408. Neurology. 2000. PMID: 10751248 Clinical Trial.

10

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

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