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Page 1
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: azzouz h. 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
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: azzouz h. 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
History of settlement of villages from Central Tunisia by studying families sharing a common founder Glycogenosis type III mutation.
Rhouma FB, Messai H, Hsouna S, Halim NB, Cherif W, Fadhel SB, Tiar A, Nagara M, Azzouz H, Sfar MT, Dridi MF, Tebib N, Ayadi A, Abdelhak S, Kefi R. Rhouma FB, et al. Among authors: azzouz h. Mitochondrial DNA A DNA Mapp Seq Anal. 2016 Sep;27(5):3194-8. doi: 10.3109/19401736.2015.1007331. Epub 2015 Dec 24. Mitochondrial DNA A DNA Mapp Seq Anal. 2016. PMID: 26704523
Mutation spectrum of glycogen storage disease type Ia in Tunisia: implication for molecular diagnosis.
Barkaoui E, Cherif W, Tebib N, Charfeddine C, Ben Rhouma F, Azzouz H, Ben Chehida A, Monastiri K, Chemli J, Amri F, Ben Turkia H, Abdelmoula MS, Kaabachi N, Abdelhak S, Ben Dridi MF. Barkaoui E, et al. Among authors: azzouz h. J Inherit Metab Dis. 2007 Nov;30(6):989. doi: 10.1007/s10545-007-0737-1. Epub 2007 Nov 19. J Inherit Metab Dis. 2007. PMID: 18008183
A novel 22bp deletion in a Tunisian phenylketonuria family.
Khemir S, Siala H, Azzouz H, Tebib N, Dhondt JL, Messaoud T, Abdelhak S, Ben Dridi MF, Kaabachi N. Khemir S, et al. Among authors: azzouz h. Pathol Biol (Paris). 2012 Dec;60(6):e87-9. doi: 10.1016/j.patbio.2012.03.007. Epub 2012 May 7. Pathol Biol (Paris). 2012. PMID: 22572109
[Renal involvement in glycogen storage disease type 1: Practical issues].
Ben Chehida A, Bensmaïl T, Ben Rehouma F, Ben Abdelaziz R, Azzouz H, Boudabbous H, Slim Abdelmoula M, Abdelhak S, Kaabachi N, Ben Turkia H, Tebib N. Ben Chehida A, et al. Among authors: azzouz h. Nephrol Ther. 2015 Jul;11(4):240-5. doi: 10.1016/j.nephro.2014.12.007. Epub 2015 May 6. Nephrol Ther. 2015. PMID: 25957470 French.
Glycogen storage disease type I in Tunisia: an epidemiological analysis.
Ben Chehida A, Tebib N, Cherif W, Ben Turkia H, Abdelmoula S, Azzouz H, Ben Dridi MF. Ben Chehida A, et al. Among authors: azzouz h. J Inherit Metab Dis. 2008 Dec;31 Suppl 2:S199-204. doi: 10.1007/s10545-008-0707-2. Epub 2008 Aug 5. J Inherit Metab Dis. 2008. PMID: 18679824
Neuromuscular Involvement in Glycogen Storage Disease Type III in Fifty Tunisian Patients: Phenotype and Natural History in Young Patients.
Ben Chehida A, Ben Messaoud S, Ben Abdelaziz R, Ben Ali N, Boudabous H, Ben Abdelaziz I, Ben Ameur Z, Sassi Y, Kaabachi N, Abdelhak S, Abdelmoula MS, Fradj M, Azzouz H, Tebib N. Ben Chehida A, et al. Among authors: azzouz h. Neuropediatrics. 2019 Feb;50(1):22-30. doi: 10.1055/s-0038-1669786. Epub 2018 Oct 11. Neuropediatrics. 2019. PMID: 30308687
94 results