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H-like syndrome successfully treated with methotrexate.
Zaouak A, Jaouadi H, Chamli A, Jouini R, Abdelhak S, Hammami H, Fenniche S. Zaouak A, et al. Among authors: abdelhak s. Dermatol Ther. 2019 Jul;32(4):e12994. doi: 10.1111/dth.12994. Epub 2019 Jun 25. Dermatol Ther. 2019. PMID: 31197883 No abstract available.
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
Hailey-Hailey disease in Tunisia.
Benmously-Mlika R, Bchetnia M, Deghais S, Ben Brick SA, Charfeddine C, Debbiche A, Haouet S, Mokni M, Abdelhak S, Kamoun MR, Ben Osman A, Fenniche S, Mokhtar I. Benmously-Mlika R, et al. Among authors: abdelhak s. Int J Dermatol. 2010 Apr;49(4):396-401. doi: 10.1111/j.1365-4632.2010.04403.x. Int J Dermatol. 2010. PMID: 20465693
Bathing suit ichthyosis caused by a TGM1 mutation in a Tunisian child.
Benmously-Mlika R, Zaouak A, Mrad R, Laaroussi N, Abdelhak S, Hovnanian A, Mokhtar I. Benmously-Mlika R, et al. Among authors: abdelhak s. Int J Dermatol. 2014 Dec;53(12):1478-80. doi: 10.1111/ijd.12569. Epub 2014 Sep 10. Int J Dermatol. 2014. PMID: 25209454
H syndrome: Clinical, histological and genetic investigation in Tunisian patients.
Jaouadi H, Zaouak A, Sellami K, Messaoud O, Chargui M, Hammami H, Jones M, Jouini R, Chadli Debbiche A, Chraiet K, Fenniche S, Mrad R, Mokni M, Turki H, Benkhalifa R, Abdelhak S. Jaouadi H, et al. Among authors: abdelhak s. J Dermatol. 2018 Aug;45(8):978-985. doi: 10.1111/1346-8138.14359. Epub 2018 May 29. J Dermatol. 2018. PMID: 29808591
Homozygous 2p11.2 deletion supports the implication of ELMOD3 in hearing loss and reveals the potential association of CAPG with ASD/ID etiology.
Lahbib S, Leblond CS, Hamza M, Regnault B, Lemée L, Mathieu A, Jaouadi H, Mkaouar R, Youssef-Turki IB, Belhadj A, Kraoua I, Bourgeron T, Abdelhak S. Lahbib S, et al. Among authors: abdelhak s. J Appl Genet. 2019 Feb;60(1):49-56. doi: 10.1007/s13353-018-0472-3. Epub 2018 Oct 4. J Appl Genet. 2019. PMID: 30284680
A Tunisian family with a novel mutation in the gene CYP4F22 for lamellar ichthyosis and co-occurrence of hearing loss in a child due to mutation in the SLC26A4 gene.
Sayeb M, Riahi Z, Laroussi N, Bonnet C, Romdhane L, Mkaouar R, Zaouak A, Marrakchi J, Abdessalem G, Messaoud O, Bouchniba O, Ghilane N, Mokni M, Besbes G, Yacoub-Youssef H, Petit C, Abdelhak S. Sayeb M, et al. Among authors: abdelhak s. Int J Dermatol. 2019 Dec;58(12):1439-1443. doi: 10.1111/ijd.14452. Epub 2019 Apr 25. Int J Dermatol. 2019. PMID: 31020658
245 results