Abdelhak S - Search Results

1

Fanconi anemia in Tunisia: high prevalence of group A and identification of new FANCA mutations.

Bouchlaka C, Abdelhak S, Amouri A, Ben Abid H, Hadiji S, Frikha M, Ben Othman T, Amri F, Ayadi H, Hachicha M, Rebaï A, Saad A, Dellagi K; Tunisian Fanconi Anemia Study Group. Bouchlaka C, et al. Among authors: abdelhak s. J Hum Genet. 2003;48(7):352-61. doi: 10.1007/s10038-003-0037-z. Epub 2003 Jun 24. J Hum Genet. 2003. PMID: 12827451

2

Clustering of mutations responsible for branchio-oto-renal (BOR) syndrome in the eyes absent homologous region (eyaHR) of EYA1.

Abdelhak S, Kalatzis V, Heilig R, Compain S, Samson D, Vincent C, Levi-Acobas F, Cruaud C, Le Merrer M, Mathieu M, König R, Vigneron J, Weissenbach J, Petit C, Weil D. Abdelhak S, et al. Hum Mol Genet. 1997 Dec;6(13):2247-55. doi: 10.1093/hmg/6.13.2247. Hum Mol Genet. 1997. PMID: 9361030

3

Clinical and genetic heterogeneity of inherited autosomal recessive susceptibility to disseminated Mycobacterium bovis bacille calmette-guérin infection.

Elloumi-Zghal H, Barbouche MR, Chemli J, Béjaoui M, Harbi A, Snoussi N, Abdelhak S, Dellagi K. Elloumi-Zghal H, et al. Among authors: abdelhak s. J Infect Dis. 2002 May 15;185(10):1468-75. doi: 10.1086/340510. Epub 2002 Apr 30. J Infect Dis. 2002. PMID: 11992283

4

MICA transmembrane region polymorphism and HLA B51 in Tunisian Behçet's disease patients.

Ben Ahmed M, Houman H, Abdelhak S, Ben Ghorbel I, Miled M, Dellagi K, Louzir H. Ben Ahmed M, et al. Among authors: abdelhak s. Adv Exp Med Biol. 2003;528:225-8. doi: 10.1007/0-306-48382-3_44. Adv Exp Med Biol. 2003. PMID: 12918695 No abstract available.

5

Genomic structure and characterisation of the promoter region of the human IL-18 gene.

el Kares R, Abdelhak S, Dellagi K. el Kares R, et al. Among authors: abdelhak s. Arch Inst Pasteur Tunis. 2000;77(1-4):55-8. Arch Inst Pasteur Tunis. 2000. PMID: 14658229

6

A novel missense mutation in the gene encoding SLURP-1 in patients with Mal de Meleda from northern Tunisia.

Charfeddine C, Mokni M, Ben Mousli R, Elkares R, Bouchlaka C, Boubaker S, Ghedamsi S, Baccouche D, Ben Osman A, Dellagi K, Abdelhak S. Charfeddine C, et al. Among authors: abdelhak s. Br J Dermatol. 2003 Dec;149(6):1108-15. doi: 10.1111/j.1365-2133.2003.05606.x. Br J Dermatol. 2003. PMID: 14674887

7

Gene Symbol: ars. Disease: Mal de Meleda.

Abdelhak S, Charfeddine C, Mokni M, Mousli RB, Elkares R, Bouchlaka C, Boubaker S, Ghedamsi S, Baccouche D, Osman AB, Dellagi K. Abdelhak S, et al. Hum Genet. 2004 May;114(6):609. Hum Genet. 2004. PMID: 15176391 No abstract available.

8

[Molecular study of Fanconi anemia in Tunisia].

Bouchlaka C, Abdelhak S, Dellagi K; Groupe d'Etude de la Maladie de Fanconi en Tunisie. Bouchlaka C, et al. Among authors: abdelhak s. Tunis Med. 2004 May;82(5):402-10. Tunis Med. 2004. PMID: 15453041 French.

9

Fanconi anemia: contribution of molecular analyses to the identification of bone marrow graft donors and the study of chimerism in grafted patients.

Bouchlaka C, Othman TB, Aissaoui L, Elloumi H, Elloumi M, Amouri A, Abid HB, Hadiji S, Slama H, Makni H, Saad A, Abdelhak S, Dellagi K; Tunisian Fanconi Anemia Study Group. Bouchlaka C, et al. Among authors: abdelhak s. Genet Test. 2004 Fall;8(3):268-75. doi: 10.1089/gte.2004.8.268. Genet Test. 2004. PMID: 15727250

10

[Association study between diabetic retinopathy and aldose reductase gene polymorphism in Tunisians].

Zghal-Mokni I, Arfa I, Elloumi-Zghal H, Abid A, Amrouche-Rached C, Kaabi B, Chakroun S, Blousa-Chabchoub S, Gaïgi S, Ayed S, Jeddi A, Dellagi K, Abdelhak S. Zghal-Mokni I, et al. Among authors: abdelhak s. J Fr Ophtalmol. 2005 Apr;28(4):386-90. doi: 10.1016/s0181-5512(05)81069-1. J Fr Ophtalmol. 2005. PMID: 15973199 French.

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