Finsterer J

No ORCID on file · 2 papers in corpus
2017
Neuropsychiatric disease and treatment ·doi:10.2147/ndt.s149067

ObjectivesMitochondrial disorders (MIDs) frequently present as mitochondrial multiorgan disorder syndrome (MIMODS) at onset or evolve into MIMODS during the course. This study aimed to find which organs and/or tissues are most frequently af…

case-report 2013
Neurology international ·doi:10.4081/ni.2013.e9

Mitochondrial DNA depletion syndrome (MDS) is usually a severe disorder of infancy or childhood, due to a reduced copy number of mtDNA molecules. MDS with only mild, nonspecific clinical manifestations and onset in adulthood has not been re…