검색결과 : 5건
| No. | Article |
|---|---|
| 1 |
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 Biochemical and Biophysical Research Communications, 484(1), 71, 2017 |
| 2 |
Mutation in gap and tight junctions in patients with non-syndromic hearing loss Belguith H, Tlili A, Dhouib H, Ben Rebeh I, Lahmar I, Charfeddine I, Driss N, Ghorbel A, Ayadi H, Masmoudi S Biochemical and Biophysical Research Communications, 385(1), 1, 2009 |
| 3 |
Mutational analysis of the mitochondrial tRNA(Leu(UUR)) gene in Tunisian patients with mitochondrial diseases Mkaouar-Rebai E, Tlili A, Masmoudi S, Belguith N, Charfeddine I, Mnif M, Triki C, Fakhfakh F Biochemical and Biophysical Research Communications, 355(4), 1031, 2007 |
| 4 |
Mutational analysis of the mitochondrial 12S rRNA and tRNA(Ser(UCN)) genes in Tunisian patients with nonsyndromic hearing loss Mkaouar-Rebai E, Tlili A, Masmoudi S, Louhichi N, Charfeddine I, Ben Amor M, Lahmar I, Driss N, Drira M, Ayadi H, Fakhfakh F Biochemical and Biophysical Research Communications, 340(4), 1251, 2006 |
| 5 |
Calcium sulphate scale prevention in a desalination unit using the SMCEC technique Ben Ahmed S, Tlili A, Ben Amor A, Ben Bacha H, Elleuch B Desalination, 167(1-3), 311, 2004 |