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An autopsy case of mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS) with a point mutation of mitochondrial DNA

  • Published:1996-05 Issue:3 Volume:18 Page:224-229
  • ISSN:0387-7604
  • Container-title:Brain and Development
  • language:en
  • Short-container-title:Brain and Development

Author:

Terauchi Akiko,Tamagawa Kimiko,Morimatsu Yoshio,Kobayashi Masanori,Sano Tadashi,Yoda Satoru

Publisher

Elsevier BV

Subject

Clinical Neurology,Developmental Neuroscience,General Medicine,Pediatrics, Perinatology, and Child Health

Reference8 articles.

1. Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS): current concepts;Hirano;J Neurol,1994

2. Atypical clinical presentations associated with the MELAS mutation at position 3243 of human mitochondrial DNA;Moraes;Neuromusc Disord,1993

3. Mitochondrial angiopathy in cerebral blood vessels of mitochondrial encephalomyopathy;Ohama;Acta Neuropathol,1987

4. Developmental Neuropathology;Friede,1989

5. Central nervous system changes in mitochondrial encephalomyopathy: light and electron microscopic study;Mizukami;Acta Neuropathol,1992

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