MELAS of infantile onset: mitochondrial angiopathy or cytopathy?-Reference-Cited by-同舟云学术

MELAS of infantile onset: mitochondrial angiopathy or cytopathy?

Published:1991-05 Issue:1 Volume:103 Page:37-41
ISSN:0022-510X
Container-title:Journal of the Neurological Sciences
language:en
Short-container-title:Journal of the Neurological Sciences

Author:

Fujii Tatsuya,Okuno Takehiko,Ito Masatoshi,Mutoh Kozo,Horiguchi Yuji,Tashiro Hironori,Mikawa Haruki

Publisher

Elsevier BV

Subject

Clinical Neurology,Neurology

Reference13 articles.

1. Mitochondrial myopathy and cardiomyopathy with neurodegenerateve features and multiple brain infarcts;Bogousslavsky;J. Neurol. Sci.,1982

2. A histochemical and morphometrical analysis of biopsied muscles in MELAS (mitochondrial encephalopathy, myopathy, lactic acidosis, and strokelike episodes);Haginoya;Brain Dev.,1987

3. Ultrastructural study of the childhood mitochondrial myopathic syndrome associated with lactic acidosis;Kobayashi;Eur. J. Pediatr.,1982

4. Findings in muscle in complex I (NADH coenzyme Q reductase) deficiency;Koga;Ann. Neurol.,1988

5. The luxury-perfusion syndrome and its possible relation to acute metabolic acidosis localised within the brain;Lassen;Lancet,1966

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