Kongenitale und Mitochondriale Myopathien
Author:
Publisher
Springer Berlin Heidelberg
Link
http://link.springer.com/content/pdf/10.1007/978-3-642-57043-8_5.pdf
Reference190 articles.
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2. Argov Z, Bank WJ, Maris J, Eleff S, Kennaway NG, Olson RE, Chance B (1986) Treatment of mitochondrial myopathy due to complex III deficiency with vitamins K3 and C: A 3IP-NMR follow-up study. Ann Neurol 19: 598–602
3. Arts WF, Bethlem J, Dingemans KP, Eriksson AW (1978) Investigations on the inheritance of nemaline myopathy. Arch Neurol 35: 72–77
4. Ballinger SW, Shoffner JM, Hedaya EV, Trounce I, Polak MA, Koontz DA, Wallace DC (1992) Maternally transmitted diabetes and deafness associated with a 10.4 kb mitochondrial DNA deletion. Nat Genet 1: 11–15
5. Bardosi A, Creutzfeldt W, DiMauro S et al. (1987) Myoneuro-, gastrointestinal encephalopathy (MNGIE syndrome) due to partial deficiency of cytochrome-c-oxidase. A new mitochondrial multisystem disorder. Acta Neuropathol (Berl) 74: 248–258
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