Genetic analysis of three pedigrees of mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes (MELAS)

Antzeko izenburuak

• Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes with recurrent abdominal symptoms and coenzyme Q10 administration.
  nork: Yamamoto, M, et al.
  Argitaratua: (1987)
• Respiration-deficient cells are caused by a single point mutation in the mitochondrial tRNA-Leu (UUR) gene in mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes (MELAS).
  nork: Kobayashi, Y, et al.
  Argitaratua: (1991)
• Diffusion-weighted MR Imaging in a Case of Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Strokelike Episodes
  nork: Yonemura, Kiminobu, et al.
  Argitaratua: (2001)
• Diffusion and Perfusion Characteristics of MELAS (Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episode) in Thirteen Patients
  nork: Kim, Ji Hye, et al.
  Argitaratua: (2011)
• Erratum: A Case of Myopathy, Encephalopathy, Lactic Acidosis and Stroke-Like Episodes (MELAS) Syndrome with Intracardiac Thrombus
  nork: Joo, Jung-Chul, et al.
  Argitaratua: (2013)