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- 2019
- Arabidopsis thaliana alternative dehydrogenases : A potential therapy for mitochondrial complex i deficiency? Perspectives and pitfalls
- 2017
- Mitochondrial dysfunction and metabolic intervention
- 2016
- Mitochondrial DNA triplication and punctual mutations in patients with mitochondrial neuromuscular disorders
- 2014
- 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
- 2011
-
Mitochondrial disorders caused by mutations in respiratory chain assembly factors
Diaz, Francisca ; Kotarsky, Heike LU ; Fellman, Vineta LU
and
Moraes, Carlos T.
(2011)
In Seminars in Fetal & Neonatal Medicine
16(4).
p.197-204
Mark
- A Tunisian patient with Pearson syndrome harboring the 4.977kb common deletion associated to two novel large-scale mitochondrial deletions
- 2010
- A de novo mutation in the adenosine triphosphatase (ATPase) 8 gene in a patient with mitochondrial disorder