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2019
Mark Arabidopsis thaliana alternative dehydrogenases : A potential therapy for mitochondrial complex i deficiency? Perspectives and pitfalls
Catania, Alessia ; Iuso, Arcangela ; Bouchereau, Juliette ; Kremer, Laura S. ; Paviolo, Marina ; Terrile, Caterina ; Bénit, Paule ; Rasmusson, Allan G. ^LU ; Schwarzmayr, Thomas and Tiranti, Valeria , et al. (2019) In Orphanet Journal of Rare Diseases 14(1).
- Contribution to journal › Article
2017
Mark Mitochondrial dysfunction and metabolic intervention
Ehinger, Johannes ^LU (2017)
- Thesis › Doctoral thesis (compilation)
2016
Mark Mitochondrial DNA triplication and punctual mutations in patients with mitochondrial neuromuscular disorders
Mkaouar-Rebai, Emna ; Felhi, Rahma ; Tabebi, Mouna ; Alila-Fersi, Olfa ; Chamkha, Imen ^LU ; Maalej, Marwa ; Ammar, Marwa ; Kammoun, Fatma ; Keskes, Leila and Hachicha, Mongia , et al. (2016) In Biochemical and Biophysical Research Communications 473(2). p.85-578
- Contribution to journal › Article
2014
Mark A mitochondrial implication in a Tunisian patient with Friedreich's ataxia-like
Maalej, M ; Mkaouar-Rebai, E ; Mnif, M ; Mezghani, N ; Ben Ayed, I ; Chamkha, I ^LU ; Abid, M and Fakhfakh, F (2014) In Pathologie Biologie 62(1). p.8-41
- Contribution to journal › Article
2013
Mark Screening of mitochondrial mutations in Tunisian patients with mitochondrial disorders : an overview study
Mkaouar-Rebai, Emna ; Chamkha, Imen ^LU ; Mezghani, Najla ; Ben Ayed, Imen and Fakhfakh, Faiza (2013) In Mitochondrial DNA 24(3). p.78-163
- Contribution to journal › Article
Mark 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
Mkaouar-Rebai, Emna ; Chamkha, Imen ^LU ; Kammoun, Thouraya ; Alila-Fersi, Olfa ; Aloulou, Hajer ; Hachicha, Mongia and Fakhfakh, Faiza (2013) In Biochemical and Biophysical Research Communications 430(2). p.91-585
- Contribution to journal › Article
2011
Mark 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
- Contribution to journal › Article
Mark A Tunisian patient with Pearson syndrome harboring the 4.977kb common deletion associated to two novel large-scale mitochondrial deletions
Ayed, Imen Ben ; Chamkha, Imen ^LU ; Mkaouar-Rebai, Emna ; Kammoun, Thouraya ; Mezghani, Najla ; Chabchoub, Imen ; Aloulou, Hajer ; Hachicha, Mongia and Fakhfakh, Faiza (2011) In Biochemical and Biophysical Research Communications 411(2). p.6-381
- Contribution to journal › Article
2010
Mark A de novo mutation in the adenosine triphosphatase (ATPase) 8 gene in a patient with mitochondrial disorder
Mkaouar-Rebai, Emna ; Kammoun, Fatma ; Chamkha, Imen ^LU ; Kammoun, Nadège ; Hsairi, Ines ; Triki, Chahnez and Fakhfakh, Faiza (2010) In Journal of Child Neurology 25(6). p.5-770
- Contribution to journal › Article

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