Publications
- Knockdown of human OXA1L impairs the biogenes of F(1)F(0)- ATP synthase and NADH2007 | First Faculty of Medicine
- Functional impairment of two or more developmentally different tissues leads us to suspect mitochondrial etiology of disease2006 | First Faculty of Medicine
- Maternal inherited Leigh syndrom due to mutation 8363G:A in mtDNAPublication without faculty affiliation
- Impact of the mtDNA mutation G8363A in MT-TK gene affected familyPublication without faculty affiliation
- Mitochondrial DNA mutations in patients with encephalopathy and hypertrophic cardiomyopathy +1Publication without faculty affiliation
- Structural and functional changes of mitochondrial ATP synthase caused by mtDNA 9205delTA mutation in ATP genePublication without faculty affiliation
- The encephalopathy with hypertrophic cardiomyopathy and mutations in mitochondrial DNAPublication without faculty affiliation
- Impact of the mtDNA mutation G8363A in MT-TK gene in affected familyPublication without faculty affiliation
- MtDNA mutation G8363A and ist impact on the oxidative phophorylation systemPublication without faculty affiliation
- Tissue - Specific patterns of Oxphos deficiencies as a result of mitochondrial tRNA mutationsPublication without faculty affiliation
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