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Family specific genetic predisposition to breast cancer: results from Tunisian whole exome sequenced breast cancer cases.
Hamdi Y, Boujemaa M, Ben Rekaya M, Ben Hamda C, Mighri N, El Benna H, Mejri N, Labidi S, Daoud N, Naouali C, Messaoud O, Chargui M, Ghedira K, Boubaker MS, Mrad R, Boussen H, Abdelhak S; PEC Consortium. Hamdi Y, et al. Among authors: abdelhak s. J Transl Med. 2018 Jun 7;16(1):158. doi: 10.1186/s12967-018-1504-9. J Transl Med. 2018. PMID: 29879995 Free PMC article.
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
Genetic diseases in the Tunisian population.
Romdhane L, Abdelhak S; Research Unit on Molecular Investigation of Genetic Orphan Diseases; Collaborators. Romdhane L, et al. Among authors: abdelhak s. Am J Med Genet A. 2011 Jan;155A(1):238-67. doi: 10.1002/ajmg.a.33771. Am J Med Genet A. 2011. PMID: 21204241 Review.
Severe phenotypes in two Tunisian families with novel XPA mutations: evidence for a correlation between mutation location and disease severity.
Messaoud O, Rekaya MB, Ouragini H, Benfadhel S, Azaiez H, Kefi R, Gouider-Khouja N, Mokhtar I, Amouri A, Boubaker MS, Zghal M, Abdelhak S. Messaoud O, et al. Among authors: abdelhak s. Arch Dermatol Res. 2012 Mar;304(2):171-6. doi: 10.1007/s00403-011-1190-4. Epub 2011 Nov 12. Arch Dermatol Res. 2012. PMID: 22081045
244 results