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Page 1
A Case of Infantile Cataract and Neonatal Hypoglycemia.
Maamouri R, Ferchichi M, Chehida AB, Cheour M. Maamouri R, et al. Among authors: chehida ab. J Curr Ophthalmol. 2024 Mar 29;35(3):291-293. doi: 10.4103/joco.joco_353_22. eCollection 2023 Jul-Sep. J Curr Ophthalmol. 2024. PMID: 38681698 Free PMC article.
Nonketotic Hyperglycinemia in Tunisia. Report upon a Series of 69 Patients.
Nasrallah F, Hadj-Taieb S, Chehida AB, Jelassi A, Ben Massoued S, Charfi M, Zidi W, Amri F, Helel KB, Mejaoual H, Seboui H, Mahdhaoui N, Gargouri A, Monastiri K, Turki I, Cheour M, Sanhaji H, Tebib N, Feki M, Kaabachi N. Nasrallah F, et al. Among authors: chehida ab. Neuropediatrics. 2020 Oct;51(5):349-353. doi: 10.1055/s-0040-1712489. Epub 2020 Aug 20. Neuropediatrics. 2020. PMID: 32818969
Molecular and computational characterization of ABCB11 and ABCG5 variants in Tunisian patients with neonatal/infantile low-GGT intrahepatic cholestasis: Genetic diagnosis and genotype-phenotype correlation assessment.
Khabou B, Kallabi F, Abdelaziz RB, Maaloul I, Aloulou H, Chehida AB, Kammoun T, Barbu V, Boudawara TS, Fakhfakh F, Khemakhem B, Sahnoun OS. Khabou B, et al. Among authors: chehida ab. Ann Hum Genet. 2024 May;88(3):194-211. doi: 10.1111/ahg.12542. Epub 2023 Dec 18. Ann Hum Genet. 2024. PMID: 38108658
A severe clinical phenotype of Noonan syndrome with neonatal hypertrophic cardiomyopathy in the second case worldwide with RAF1 S259Y neomutation.
Jaouadi H, Chehida AB, Kraoua L, Etchevers HC, Argiro L, Kasdallah N, Blibech S, Delague V, Lévy N, Tebib N, Mrad R, Abdelhak S, Benkhalifa R, Zaffran S. Jaouadi H, et al. Among authors: chehida ab. Genet Res (Camb). 2019 Apr 29;101:e6. doi: 10.1017/S0016672319000041. Genet Res (Camb). 2019. PMID: 31030682 Free PMC article.
Homogénéité mutationnelle de la glycogénose de type Ia en Tunisie.
Cherif W, Rhouma FB, Chehida AB, Azzouz H, Monastiri K, Amri F, Chemli J, Kaabachi N, Abdelhak S, Tebib N, Dridi MF. Cherif W, et al. Among authors: chehida ab. Pathol Biol (Paris). 2011 Aug;59(4):e93-6. doi: 10.1016/j.patbio.2009.05.004. Epub 2009 Nov 5. Pathol Biol (Paris). 2011. PMID: 19896294
Founder effect confirmation of c.241A>G mutation in the L2HGDH gene and characterization of oxidative stress parameters in six Tunisian families with L-2-hydroxyglutaric aciduria.
Jellouli NK, Hadj Salem I, Ellouz E, Kamoun Z, kamoun F, tlili A, Kaabachi N, Triki C, Fakhfakh F; Tunisian Network on Mental Retardation study. Jellouli NK, et al. J Hum Genet. 2014 Apr;59(4):216-22. doi: 10.1038/jhg.2014.4. Epub 2014 Feb 27. J Hum Genet. 2014. PMID: 24573090
Molecular and biochemical characterization of a novel intronic single point mutation in a Tunisian family with glycogen storage disease type III.
Ben Rhouma F, Azzouz H, Petit FM, Khelifa MB, Chehida AB, Nasrallah F, Parisot F, Lasram K, Kefi R, Bouyacoub Y, Romdhane L, Baussan C, Kaabachi N, Ben Dridi MF, Tebib N, Abdelhak S. Ben Rhouma F, et al. Among authors: chehida ab. Mol Biol Rep. 2013 Jul;40(7):4197-202. doi: 10.1007/s11033-013-2500-z. Epub 2013 May 8. Mol Biol Rep. 2013. PMID: 23649758