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Page 1
[Primary Sjögren syndrome in a child].
Majdoub I, Kallel S, Hsairi M, Snoussi M, Charfi M, Ben Halima A, Frikha A, Weli M, Safi F, Gargouri L, Ben Halima N, Mahfoudh A, Ghorbel A, Bahloul Z. Majdoub I, et al. Arch Pediatr. 2017 Dec;24(12):1249-1252. doi: 10.1016/j.arcped.2017.09.009. Epub 2017 Nov 20. Arch Pediatr. 2017. PMID: 29158045 French.
Co segregation of the m.1555A>G mutation in the MT-RNR1 gene and mutations in MT-ATP6 gene in a family with dilated mitochondrial cardiomyopathy and hearing loss: A whole mitochondrial genome screening.
Alila-Fersi O, Chamkha I, Majdoub I, Gargouri L, Mkaouar-Rebai E, Tabebi M, Tlili A, Keskes L, Mahfoudh A, Fakhfakh F. Alila-Fersi O, et al. Among authors: majdoub i. Biochem Biophys Res Commun. 2017 Feb 26;484(1):71-78. doi: 10.1016/j.bbrc.2017.01.070. Epub 2017 Jan 16. Biochem Biophys Res Commun. 2017. PMID: 28104394