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Page 1
Omenn syndrome: two case reports.
Siala N, Azzabi O, Kebaier H, Mrad R, Rebah O, Barbouche R, Bejaoui M, Halioui S, Maherzi A. Siala N, et al. Among authors: mrad r. Acta Dermatovenerol Croat. 2013;21(4):259-62. Acta Dermatovenerol Croat. 2013. PMID: 24476615
A case of a Tunisian Rett patient with a novel double-mutation of the MECP2 gene.
Fendri-Kriaa N, Hsairi I, Kifagi C, Ellouze E, Mkaouar-Rebai E, Triki C, Fakhfakh F; Tunisian network on mental retardation study. Fendri-Kriaa N, et al. Biochem Biophys Res Commun. 2011 Jun 3;409(2):270-4. doi: 10.1016/j.bbrc.2011.04.140. Epub 2011 May 7. Biochem Biophys Res Commun. 2011. PMID: 21575601
Current phenotypic and genetic spectrum of syndromic deafness in Tunisia: paving the way for precision auditory health.
Mkaouar R, Riahi Z, Marrakchi J, Mezzi N, Romdhane L, Boujemaa M, Dallali H, Sayeb M, Lahbib S, Jaouadi H, Boudabbous H, Zekri L, Chargui M, Messaoud O, Elyounsi M, Kraoua I, Zaouak A, Turki I, Mokni M, Boucher S, Petit C, Giraudet F, Mbarek C, Besbes G, Halayem S, Zainine R, Turki H, Tounsi A, Bonnet C, Mrad R, Abdelhak S, Trabelsi M, Charfeddine C. Mkaouar R, et al. Among authors: mrad r. Front Genet. 2024 Apr 22;15:1384094. doi: 10.3389/fgene.2024.1384094. eCollection 2024. Front Genet. 2024. PMID: 38711914 Free PMC article.
Alport syndrome: a genetic study of 31 families.
M'Rad R, Sanak M, Deschenes G, Zhou J, Bonaiti-Pellie C, Holvoet-Vermaut L, Heuertz S, Gubler MC, Broyer M, Grunfeld JP, et al. M'Rad R, et al. Hum Genet. 1992 Dec;90(4):420-6. doi: 10.1007/BF00220471. Hum Genet. 1992. PMID: 1483700
Mutational survey of recessive dystrophic epidermolysis bullosa in Tunisian families unveils a spectrum of private, ethnic specific and world wide recurrent mutations.
Ouragini H, Cherif F, Brick SA, Nouira S, Floriddia G, Pascucci M, Kefi R, Daoud W, Mahdhaoui N, Kassar S, Mrad R, Kamoun MR, Ben Osman-Dhahri A, Denguezli M, Monastiri K, Seboui H, Mokni M, Boubaker S, Castiglia D, Abdelhak S. Ouragini H, et al. Among authors: mrad r. J Dermatol Sci. 2010 Feb;57(2):144-6. doi: 10.1016/j.jdermsci.2009.12.001. Epub 2010 Jan 8. J Dermatol Sci. 2010. PMID: 20060269 No abstract available.
Turner syndrome: results of the first Tunisian study group on Turner syndrome (TuSGOT).
Essaddam L, Zitouni O, Kraoua L, Trabelsi M, Sassi H, Kmiha S, Charfi F, El Guiche D, Kebaïli R, Jaballah N, Rjeb M, Zouari N, El Aribi Y, Hizem S, Wannes S, Fkih Romdhane I, Sfar MT, Ben Hamouda H, Hadj Salem R, Khlayfia Z, Khmiss T, Monastiri K, Siala N, Chouchane S, Souaa H, Khochtali I, Mahjoub B, Sfar H, Ben Jemâa L, Abroug S, Boughamoura L, Kamoun I, Kamoun T, Mrad R, Ben Becher S. Essaddam L, et al. Among authors: mrad r. J Pediatr Endocrinol Metab. 2023 Apr 21;36(6):577-583. doi: 10.1515/jpem-2022-0360. Print 2023 Jun 27. J Pediatr Endocrinol Metab. 2023. PMID: 37084413
[Myalgia in familial Mediterranean fever].
B'chir Hamzaoui S, Bouslama K, Abdallah M, M'rad R, M'rad S, Ben Dridi M. B'chir Hamzaoui S, et al. Rev Neurol (Paris). 2007 Jan;163(1):93-5. doi: 10.1016/s0035-3787(07)90360-4. Rev Neurol (Paris). 2007. PMID: 17304178 French.
148 results