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Page 1
[Atypical presentation of Wegener disease in childhood].
Ben Turkia H, Amdouni N, Azzouz H, Tebib N, Abdelmoula MS, El Mazni F, Hamzaoui A, Ben Dridi MF. Ben Turkia H, et al. Among authors: abdelmoula ms. J Mal Vasc. 2008 Dec;33(4-5):242-6. doi: 10.1016/j.jmv.2008.09.007. Epub 2008 Nov 20. J Mal Vasc. 2008. PMID: 19022597 French.
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
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
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
New C1q mutation in a Tunisian family.
Jlajla H, Sellami MK, Sfar I, Laadhar L, Zerzeri Y, Abdelmoula MS, Gorgi Y, Dridi MF, Makni S. Jlajla H, et al. Among authors: abdelmoula ms. Immunobiology. 2014 Mar;219(3):241-6. doi: 10.1016/j.imbio.2013.10.010. Epub 2013 Nov 6. Immunobiology. 2014. PMID: 24331529 Review.
[Rosai -Dorfman disease: a two cases report].
Ben Turkia H, Ben Romdhane M, Azzouz H, Ben Chehida A, Abdelmoula MS, Ben Abdelaziz R, Tebib N, Ben Messoud M, Sahtout S, Chelly I, Zitouni M, Mnif E, Ben Dridi MF. Ben Turkia H, et al. Among authors: abdelmoula ms. Tunis Med. 2011 May;89(5):497-501. Tunis Med. 2011. PMID: 21557191 Free article. 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 Free article.
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