Author:
Sinnecker Tim,Andelova Michaela,Mayr Michael,Rüegg Stephan,Sinnreich Michael,Hench Juergen,Frank Stephan,Schaller André,Stippich Christoph,Wuerfel Jens,Bonati Leo H.
Publisher
Springer Science and Business Media LLC
Subject
Neurology (clinical),General Medicine
Reference37 articles.
1. McFarland R, Taylor RW, Turnbull DM. A neurological perspective on mitochondrial disease. Lancet Neurol. 2010;9:829–40.
2. Testai FD, Gorelick PB. Inherited metabolic disorders and stroke part 1: Fabry disease and mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes. Arch Neurol. 2010;67:19–24.
3. Hirano M, Pavlakis SG. Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes (MELAS): current concepts. J Child Neurol. 1994;9:4–13.
4. Kung NH, Bucelli RC, Van Stavern RB, Goebel JA, Van Stavern GP. A young man with progressive vision and hearing loss. JAMA Neurol. 2016;73:880–3.
5. Kisanuki YY, Gruis KL, Smith TL, Brown DL. Late-onset mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes with bitemporal lesions. Arch Neurol. 2006;63:1200–1.
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