Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-like Episodes (MELAS) due to a m.10158T>C ND3 Mutation with a Normal Muscle Biopsy

Benzer Materyaller

• Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-like Episodes (MELAS) due to a m.10158T>C ND3 Mutation with a Normal Muscle Biopsy
  Yazar:: Mukai, Masako, ve diğerleri
  Baskı/Yayın Bilgisi: (2017)
• Letter to the Editor: Diagnosing Mitochondrial Encephalomyopathy With Lactic Acidosis and Stroke-Like Episodes (MELAS) Requires Not Only Phenotypic But Also Genotypic Verification
  Yazar:: Finsterer, Josef, ve diğerleri
  Baskı/Yayın Bilgisi: (2018)
• MELAS syndrome due to the m.3291T > C mutation
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  Baskı/Yayın Bilgisi: (2016)
• Can MR spectroscopy and muscle biopsy findings be correlated with MELAS and CPEO?
  Yazar:: Finsterer, Josef, ve diğerleri
  Baskı/Yayın Bilgisi: (2017)
• Genetic analysis of three pedigrees of mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes (MELAS)
  Yazar:: Sato, W, ve diğerleri
  Baskı/Yayın Bilgisi: (1992)