Mokni M - Search Results

1

Particular Mal de Meleda phenotypes in Tunisia and mutations founder effect in the Mediterranean region.

Bchetnia M, Laroussi N, Youssef M, Charfeddine C, Ben Brick AS, Boubaker MS, Mokni M, Abdelhak S, Zili J, Benmously R. Bchetnia M, et al. Among authors: mokni m. Biomed Res Int. 2013;2013:206803. doi: 10.1155/2013/206803. Epub 2013 Sep 4. Biomed Res Int. 2013. PMID: 24093092 Free PMC article.

2

[Granuloma annulare: apropos of 18 cases].

Ben Mously R, el Euch D, Chakroun R, Mokni M, Cherif F, Azaïz MI, Ben-Osman-Dhahri A. Ben Mously R, et al. Among authors: mokni m. Tunis Med. 2003 Jul;81(7):495-8. Tunis Med. 2003. PMID: 14534961 French.

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: mokni m. 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: mokni m. 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

Clinical, histological and genetic investigation of Buschke-Fischer-Brauer's disease in Tunisian families.

Bchetnia M, Charfeddine C, Kassar S, Hanchi I, Tounsi-Guettiti H, Rebai A, Osman AD, Kubisch C, Abdelhak S, Boubaker S, Mokni M. Bchetnia M, et al. Among authors: mokni m. J Dermatol Sci. 2009 Apr;54(1):54-6. doi: 10.1016/j.jdermsci.2008.11.008. Epub 2009 Jan 10. J Dermatol Sci. 2009. PMID: 19136236 No abstract available.

6

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: mokni m. 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

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: mokni m. Arch Dermatol. 2009 Jun;145(6):654-6. doi: 10.1001/archdermatol.2009.52. Arch Dermatol. 2009. PMID: 19528419

8

Coexistence of mal de Meleda and congenital cataract in a consanguineous Tunisian family: two case reports.

Bchetnia M, Merdassi A, Charfeddine C, Mgaieth F, Kassar S, Ouechtati F, Chouchene I, Boussen H, Mokni M, Osman AD, Boubaker MS, Abdelhak S, Elmatri L. Bchetnia M, et al. Among authors: mokni m. J Med Case Rep. 2010 Apr 20;4:108. doi: 10.1186/1752-1947-4-108. J Med Case Rep. 2010. PMID: 20406438 Free PMC article.

9

[Erythrodermic psoriasis: epidemiological clinical and therapeutic features about 60 cases].

Hawilo A, Zaraa I, Benmously R, Mebazaa A, El Euch D, Mokni M, Ben Osman A. Hawilo A, et al. Among authors: mokni m. Tunis Med. 2011 Nov;89(11):841-7. Tunis Med. 2011. PMID: 22179920 Free article. French.

10

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: mokni m. J Genet. 2011 Dec;90(3):483-7. doi: 10.1007/s12041-011-0101-y. J Genet. 2011. PMID: 22227937 No abstract available.

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