Publications
- Different laboratory and muscle biopsy findings in a family with an m.8851T > C mutation in the mitochondrial MTATP6 gene2013 | First Faculty of Medicine, Second Faculty of Medicine
- Mitochondrial encephalocardio-myopathy with early neonatal onset due to TMEM70 mutation2010 | First Faculty of Medicine
- Deficiency of mitochondrial ATP synthase of nuclear genetic origin2006 | First Faculty of Medicine
- Mitochondrial diseases and genetic defects of ATP synthase2006 | First Faculty of Medicine
- Deficiency of mitochondrial ATP synthase of nuclear genetic origin2006 | Faculty of Physical Education and Sport
- Mitochondrial diseases and genetic defects of ATP synthase2006 | Faculty of Physical Education and Sport
- Two components in pathogenic mechanism of mitochondrial ATP synthase deficiency: energy deprivation and ROS productionPublication without faculty affiliation
- Structural and functional changes of mitochondrial ATP synthase caused by mtDNA 9205delTA mutation in ATP genePublication without faculty affiliation
- Isolated deficiency of mitochondrial ATP synthase caused by nuclear genetic originPublication without faculty affiliation
- Isolated deficiency of mitochondrial ATP synthase caused by nuclear genetic defectsPublication without faculty affiliation
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