Abdelhak S - Search Results

1

Inflammatory landscape in Xeroderma pigmentosum patients with cutaneous melanoma.

Chikhaoui A, Jones M, Režen T, Ben Ahmed M, Naouali C, Komel R, Zghal M, Boubaker S, Abdelhak S, Yacoub-Youssef H. Chikhaoui A, et al. Among authors: abdelhak s. Sci Rep. 2022 Aug 16;12(1):13854. doi: 10.1038/s41598-022-17928-z. Sci Rep. 2022. PMID: 35974070 Free PMC article.

2

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.

3

Further evidence of the clinical and genetic heterogeneity of recessive transgressive PPK in the Mediterranean region.

Charfeddine C, Mokni M, Kassar S, Zribi H, Bouchlaka C, Boubaker S, Rebai A, Ben Osman A, Abdelhak S. Charfeddine C, et al. Among authors: abdelhak s. J Hum Genet. 2006;51(10):841-845. doi: 10.1007/s10038-006-0002-8. Epub 2006 Jul 25. J Hum Genet. 2006. PMID: 16865292

4

Immunohistological study of involucrin expression in Darier's disease skin.

Kassar S, Charfeddine C, Zribi H, Tounsi-Kettiti H, Bchetnia M, Jerbi E, Cassio D, Mokni M, Abdelhak S, Ben Osman A, Boubaker S. Kassar S, et al. Among authors: abdelhak s. J Cutan Pathol. 2008 Jul;35(7):635-40. doi: 10.1111/j.1600-0560.2007.00880.x. Epub 2008 Feb 29. J Cutan Pathol. 2008. PMID: 18312435

5

Haplotypic classification of dystrophic epidermolysis bullosa in Tunisian consanguineous families: implication for diagnosis.

Ouragini H, Cherif F, Daoud W, Kassar S, Charfeddine C, Rebaï A, Boubaker S, Ben Osman-Dhahri A, Abdelhak S. Ouragini H, et al. Among authors: abdelhak s. Arch Dermatol Res. 2008 Aug;300(7):365-70. doi: 10.1007/s00403-008-0861-2. Epub 2008 May 22. Arch Dermatol Res. 2008. PMID: 18496702

6

Dystrophic epidermolysis bullosa phenotypes in a large consanguineous Tunisian family.

Ouragini H, Cherif F, Kassar S, Floriddia G, Pascucci M, Daoud W, Osman-Dhahri AB, Boubaker S, Castiglia D, Abdelhak S. Ouragini H, et al. Among authors: abdelhak s. J Dermatol Sci. 2009 May;54(2):114-20. doi: 10.1016/j.jdermsci.2009.01.006. Epub 2009 Mar 3. J Dermatol Sci. 2009. PMID: 19261445

7

High frequency of the V548A fs X572 XPC mutation in Tunisia: implication for molecular diagnosis.

Ben Rekaya M, Messaoud O, Talmoudi F, Nouira S, Ouragini H, Amouri A, Boussen H, Boubaker S, Mokni M, Mokthar I, Abdelhak S, Zghal M. Ben Rekaya M, et al. Among authors: abdelhak s. J Hum Genet. 2009 Jul;54(7):426-9. doi: 10.1038/jhg.2009.50. Epub 2009 May 29. J Hum Genet. 2009. PMID: 19478817

8

Clinical and mutational heterogeneity of Darier disease in Tunisian families.

Bchetnia M, Charfeddine C, Kassar S, Zribi H, Guettiti HT, Ellouze F, Cheour M, Boubaker S, Osman AD, Abdelhak S, Mokni M. Bchetnia M, et al. Among authors: abdelhak s. Arch Dermatol. 2009 Jun;145(6):654-6. doi: 10.1001/archdermatol.2009.52. Arch Dermatol. 2009. PMID: 19528419

9

Identification of a primarily neurological phenotypic expression of xeroderma pigmentosum complementation group A in a Tunisian family.

Messaoud O, Ben Rekaya M, Kefi R, Chebel S, Boughammoura-Bouatay A, Bel Hadj Ali H, Gouider-Khouja N, Zili J, Frih-Ayed M, Mokhtar I, Abdelhak S, Zghal M. Messaoud O, et al. Among authors: abdelhak s. Br J Dermatol. 2010 Apr;162(4):883-6. doi: 10.1111/j.1365-2133.2010.09646.x. Epub 2010 Feb 25. Br J Dermatol. 2010. PMID: 20199544

10

Genetic homogeneity of mutational spectrum of group-A xeroderma pigmentosum in Tunisian patients.

Messaoud O, Ben Rekaya M, Cherif W, Talmoudi F, Boussen H, Mokhtar I, Boubaker S, Amouri A, Abdelhak S, Zghal M. Messaoud O, et al. Among authors: abdelhak s. Int J Dermatol. 2010 May;49(5):544-8. doi: 10.1111/j.1365-4632.2010.04421.x. Int J Dermatol. 2010. PMID: 20534089

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