Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

Search Results

245 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Results By Year timeline is not available.
Page 1
New mutations of Darier disease in Tunisian patients.
Bchetnia M, Benmously R, Ben Brick AS, Charfeddine C, Ben Ameur Y, Fajraoui M, Debbiche A, Ben Ayed M, Mokni M, Fenniche S, Mokhtar I, Abdelhak S. Bchetnia M, et al. Among authors: abdelhak s. Arch Dermatol Res. 2009 Sep;301(8):615-9. doi: 10.1007/s00403-009-0963-5. Epub 2009 Jun 2. Arch Dermatol Res. 2009. PMID: 19488774
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
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
Maternal effect and familial aggregation in a type 2 diabetic Moroccan population.
Benrahma H, Arfa I, Charif M, Bounaceur S, Eloualid A, Boulouiz R, Nahili H, Abidi O, Rouba H, Chadli A, Oudghiri M, Farouqui A, Abdelhak S, Barakat A. Benrahma H, et al. Among authors: abdelhak s. J Community Health. 2011 Dec;36(6):943-8. doi: 10.1007/s10900-011-9393-3. J Community Health. 2011. PMID: 21442339
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
245 results