
Modern concepts regarding mitochondrial encephalomyopathies (ME) are summarized. Utilizing recent techniques of molecular biology we studied some cases of ME referred to the Institute of Clinical Neurology of Milan University. With these techniques we demonstrated different mitochondrial DNA deletions either in patients' muscle or in culture.
Adult, Aged, 80 and over, Family Health, Brain Diseases, Ophthalmoplegia, Adolescent, Kearns-Sayre Syndrome, Middle Aged, DNA, Mitochondrial, Mitochondria, Muscle, Pedigree, Electron Transport Complex IV, Microscopy, Electron, Muscular Diseases, Karyotyping, Humans, Chromosome Deletion, Aged
Adult, Aged, 80 and over, Family Health, Brain Diseases, Ophthalmoplegia, Adolescent, Kearns-Sayre Syndrome, Middle Aged, DNA, Mitochondrial, Mitochondria, Muscle, Pedigree, Electron Transport Complex IV, Microscopy, Electron, Muscular Diseases, Karyotyping, Humans, Chromosome Deletion, Aged
| selected citations These citations are derived from selected sources. This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | 0 | |
| popularity This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network. | Average | |
| influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | Average | |
| impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network. | Average |
