Imen Chamkha
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- 2018
- Do GSTM1 and GSTT1 polymorphisms influence the risk of developing mitochondrial diseases in a Tunisian population?
- Bioenergetic bypass using cell-permeable succinate, but not methylene blue, attenuates metformin-induced lactate production
- 2017
- 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
- 2016
- Whole mitochondrial genome analysis in two families with dilated mitochondrial cardiomyopathy : detection of mutations in MT-ND2 and MT-TL1 genes
- Mitochondrial DNA triplication and punctual mutations in patients with mitochondrial neuromuscular disorders
- 2014
- A novel MT-CO2 m.8249G>A pathogenic variation and the MT-TW m.5521G>A mutation in patients with mitochondrial myopathy
- A mitochondrial implication in a Tunisian patient with Friedreich's ataxia-like
- 2013
- Screening of mitochondrial mutations in Tunisian patients with mitochondrial disorders : an overview study
- A novel MT-CO1 m.6498C>A variation associated with the m.7444G>A mutation in the mitochondrial COI/tRNA(Ser(UCN)) genes in a patient with hearing impairment, diabetes and congenital visual loss
- 2012
- A novel m.12908T>a mutation in the mitochondrial ND5 gene in patient with infantile-onset Pompe disease