Marked reduction in CSF lactate and pyruvate levels after CoQ therapy in a patient with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS)
Author:
Publisher
Wiley
Subject
Neurology (clinical),Neurology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1600-0404.1991.tb03962.x/fullpdf
Reference17 articles.
1. Familial poliodystrophy, mitochondrial myopathy, and lactate acidemia;Shapira;Neurology,1975
2. Reversible alexia, mitochondrial myopathy, and lactic acidemia;Skoglund;Neurology,1979
3. Mitochondrial myopathy and encephalopathy: a deficiency of NADH-CoQ dehydrogenase;Holliday;Neurology,1983
4. Improvement of abnormal cardiac conduction defect with coenzyme Q10 in Kerns-Sayer syndrome;Ogasawara;Neurology,1985
5. Decreased activities in mitochondrial inner membrane electron transport system in muscle from patients with Kearns-Sayre syndrome;Yorifuji;J Neurolo Sci,1985
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