검색결과 : 5건
| No. | Article |
|---|---|
| 1 |
A maternally inherited diabetes and deafness patient with the 12S rRNA m.1555A > G and the ND1 m.3308T > C mutations associated with multiple mitochondrial deletions Mezghani N, Mnif M, Mkaouar-Rebai E, Kallel N, Charfi N, Abid M, Fakhfakh F Biochemical and Biophysical Research Communications, 431(4), 670, 2013 |
| 2 |
A whole mitochondrial genome screening in a MELAS patient: A novel mitochondrial tRNA(Val) mutation Mezghani N, Mnif M, Kacem M, Mkaouar-Rebai E, Salem IH, Kallel N, Charfi N, Abid M, Fakhfakh F Biochemical and Biophysical Research Communications, 407(4), 747, 2011 |
| 3 |
The mitochondrial ND1 m.3337G > A mutation associated to multiple mitochondrial DNA deletions in a patient with Wolfram syndrome and cardiomyopathy Mezghani N, Mnif M, Mkaouar-Rebai E, Kallel N, Salem IH, Charfi N, Abid M, Fakhfakh F Biochemical and Biophysical Research Communications, 411(2), 247, 2011 |
| 4 |
Mineralogical identification, spectroscopic characterization, and potential environmental use of natural clay materials on chromate removal from aqueous solutions Eloussaief M, Kallel N, Yaacoubi A, Benzina M Chemical Engineering Journal, 168(3), 1024, 2011 |
| 5 |
Admittance spectroscopy and complex impedance analysis of Ti-modified La0.7Sr0.3MnO3 Rahmouni H, Jemai R, Nouiri M, Kallel N, Rzigua F, Selmi A, Khirouni K, Alaya S Journal of Crystal Growth, 310(3), 556, 2008 |