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Page 1
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: abdelmoula ms. Neuropediatrics. 2019 Feb;50(1):22-30. doi: 10.1055/s-0038-1669786. Epub 2018 Oct 11. Neuropediatrics. 2019. PMID: 30308687
Incidence of mucopolysaccharidoses in Tunisia.
Ben Turkia H, Tebib N, Azzouz H, Abdelmoula MS, Ben Chehida A, Chemli J, Monastiri K, Chaabouni M, Sanhagi H, Zouari B, Kaabachi N, Ben Dridi MF. Ben Turkia H, et al. Among authors: abdelmoula ms. Tunis Med. 2009 Nov;87(11):782-5. Tunis Med. 2009. PMID: 20209839
[Phenotype and mutational spectrum in Tunisian pediatric gaucher disease].
Ben Turkia H, Riahi I, Azzouz H, Ladab S, Cherif W, Ben Chehida A, Abdelmoula MS, Caillaud C, Chemli J, Abdelhak S, Tebib N, Ben Dridi MF. Ben Turkia H, et al. Among authors: abdelmoula ms. Tunis Med. 2010 Mar;88(3):158-62. Tunis Med. 2010. PMID: 20415187 French.
Congenital hyperinsulinism: review of 12 Tunisian cases.
Ben Turkia H, Brahim K, Azzouz H, Tebib N, Abdelmoula MS, Ben Chehida A, Fekih M, Sayed S, Kaabar N, Francoise Ben Dridi M. Ben Turkia H, et al. Among authors: abdelmoula ms. Tunis Med. 2011 Apr;89(4):369-73. Tunis Med. 2011. PMID: 21484688
A lower energetic, protein and uncooked cornstarch intake is associated with a more severe outcome in glycogen storage disease type III: an observational study of 50 patients.
Ben Chehida A, Ben Messaoud S, Ben Abdelaziz R, Mansouri H, Boudabous H, Hakim K, Ben Ali N, Ben Ameur Z, Sassi Y, Kaabachi N, Abdelhak S, Abdelmoula MS, Azzouz H, Tebib N. Ben Chehida A, et al. Among authors: abdelmoula ms. J Pediatr Endocrinol Metab. 2018 Sep 25;31(9):979-986. doi: 10.1515/jpem-2018-0151. J Pediatr Endocrinol Metab. 2018. PMID: 30110253
Quality of life and associated factors in parents of children with late diagnosed phenylketonuria. A cross sectional study in a developing country (Tunisia).
Ben Abdelaziz R, Ben Chehida A, Kachouri H, Ben Messaoud S, Ferchichi M, Ben Ameur Z, Sassi Y, Abdelmoula MS, Azzouz H, Tebib N. Ben Abdelaziz R, et al. Among authors: abdelmoula ms. J Pediatr Endocrinol Metab. 2020 Jul 28;33(7):901-913. doi: 10.1515/jpem-2020-0035. J Pediatr Endocrinol Metab. 2020. PMID: 32639944
[A novel mutation in PEX 26 gene in Zellweger syndrome: a case report].
Ben Turkia H, Yangui M, Azzouz H, Ben Chehida A, Ben Abelaziz R, Abdelmoula MS, Nasrallah F, Kaabachi N, Wanders R, Tebib N, Ben Dridi MF. Ben Turkia H, et al. Among authors: abdelmoula ms. Tunis Med. 2011 Mar;89(3):288-91. Tunis Med. 2011. PMID: 21387236 French.
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