Mitochondrial encephalomyopathy, lactic acidosis, stroke-like episodes (MELAS): Clinical, radiological, pathological, and genetic observations-Reference-Cited by-同舟云学术

Mitochondrial encephalomyopathy, lactic acidosis, stroke-like episodes (MELAS): Clinical, radiological, pathological, and genetic observations

Published:1993-07 Issue:1 Volume:34 Page:25-32
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol.

Author:

Koo Betty,Becker Laurence E.,Chuang Sylvester,Merante Frank,Robinson Brian H.,MacGregor Daune,Tein Ingrid,Ho Vincent B.,McGreal Douglas A.,Wherrett John R.,Logan William J.

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Reference46 articles.

1. Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes: A distinctive clinical syndrome

2. MELAS syndrome: Characteristic migrainous and epileptic features and maternal transmission

3. Mitochondrial encenhdomyopathy with lachte-pyruvate elevation and brain infarctions

4. Strongly succinate dehydrogenase-reactive blood vessels in muscles from patients with mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes

5. Vascular involvement in mitochondrial myopathy

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