Abdelhak S - Search Results

1

Hamdi Y, Abdeljaoued-Tej I, Zatchi AA, Abdelhak S, Boubaker S, Brown JS, Benkahla A. Hamdi Y, et al. Among authors: abdelhak s. Front Oncol. 2021 Apr 15;11:650117. doi: 10.3389/fonc.2021.650117. eCollection 2021. Front Oncol. 2021. PMID: 33937056 Free PMC article.

2

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

3

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

4

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

5

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

6

Histological characterization of Darier's disease in Tunisian families.

Kassar S, Tounsi-Kettiti H, Charfeddine C, Zribi H, Bchetnia M, Jerbi E, Mokni M, Ben Osman A, Abdelhak S, Boubaker S. Kassar S, et al. Among authors: abdelhak s. J Eur Acad Dermatol Venereol. 2009 Oct;23(10):1178-83. doi: 10.1111/j.1468-3083.2009.03283.x. Epub 2009 May 26. J Eur Acad Dermatol Venereol. 2009. PMID: 19486234

7

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

8

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

9

A novel POLH gene mutation in a xeroderma pigmentosum-V Tunisian patient: phenotype-genotype correlation.

Ben Rekaya M, Messaoud O, Mebazaa A, Riahi O, Azaiez H, Kefi R, Zghal M, Boubaker S, Amouri A, Ben Osman-Dhahri A, Abdelhak S, Mokni M. Ben Rekaya M, et al. Among authors: abdelhak s. J Genet. 2011 Dec;90(3):483-7. doi: 10.1007/s12041-011-0101-y. J Genet. 2011. PMID: 22227937 Free article. No abstract available.

10

Novel and recurrent mutations in the TAT gene in Tunisian families affected with Richner-Hanhart syndrome.

Bouyacoub Y, Zribi H, Azzouz H, Nasrallah F, Abdelaziz RB, Kacem M, Rekaya B, Messaoud O, Romdhane L, Charfeddine C, Bouziri M, Bouziri S, Tebib N, Mokni M, Kaabachi N, Boubaker S, Abdelhak S. Bouyacoub Y, et al. Among authors: abdelhak s. Gene. 2013 Oct 15;529(1):45-9. doi: 10.1016/j.gene.2013.07.066. Epub 2013 Aug 13. Gene. 2013. PMID: 23954227

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