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Understanding mitochondrial diseases
Clinical Nutrition, 2017M T, García-Silva +2 more
openaire +2 more sources
Precise modelling of mitochondrial diseases using optimized mitoBEs
NatureXiaoxue Zhang +7 more
semanticscholar +1 more source
Der Nervenarzt, 2019
Mitochondrial diseases (MD) are caused by mutations in the mitochondrial DNA or nuclear DNA. The clinical manifestation is often most severe in tissues with high energy demands. The most common MDs are Leber's hereditary optic neuropathy (LHON), chronic progressive external ophthalmoplegia (CPEO) and mitochondrial encephalomyopathy with lactic acidosis
Florentine, Radelfahr, Thomas, Klopstock
openaire +1 more source
Mitochondrial diseases (MD) are caused by mutations in the mitochondrial DNA or nuclear DNA. The clinical manifestation is often most severe in tissues with high energy demands. The most common MDs are Leber's hereditary optic neuropathy (LHON), chronic progressive external ophthalmoplegia (CPEO) and mitochondrial encephalomyopathy with lactic acidosis
Florentine, Radelfahr, Thomas, Klopstock
openaire +1 more source
Cardiac complications in inherited mitochondrial diseases
Heart Failure Reviews, 2020M. Behjati +3 more
semanticscholar +1 more source
Mitochondrial diseases: the contribution of organelle stress responses to pathology
Nature reviews. Molecular cell biology, 2017A. Suomalainen, B. Battersby
semanticscholar +1 more source
Recent topics: the diagnosis, molecular genesis, and treatment of mitochondrial diseases
Journal of Human Genetics, 2018K. Murayama +4 more
semanticscholar +1 more source
FGF-21 as a Potential Biomarker for Mitochondrial Diseases.
Current Medicinal Chemistry, 2018L. Scholle +4 more
semanticscholar +1 more source