References
Cros D, Palliyath S, DiMauro S, Ramirez C, Shamsnia M, Wizner B (1992) Respiratory failure revealing mitochondrial myopathy in adults. Chest 101:824–828
Desbiens R, Andermann E, Shoubridge EA, Berkovic SF, Carpenter S, Karpati G, Andermann F (1992) An unexpected phenotype of MELAS syndrome: maturity-onset dementia and strokes. Neurology 42 [Suppl 3]:281
Goto Y, Horai S, Matsuoka T, Koga Y, Nihei K, Kobayashi M, Nonaka I (1992) Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS): a correlative study of the clinical features and mitochondrial DNA mutation. Neurology 42:545–550
Goto Y, Tojo M, Tohyama J, Horai S, Nonaka I (1992) A novel point mutation in the mitochondrial tRNALeu(UUR) gene in a family with mitochondrial myopathy. Ann Neurol 31:672–675
Hasegawa H, Matsuoka T, Goto Y, Nonaka I (1991) Strongly succinate dehydrogenase-reactive blood vessels in muscles from patients with mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes. Ann Neurol 29:601–605
Koo B, Becker LE, Chuang S, Merante F, Robinson BH, MacGregor D, Tein I, Ho VB, McGreal DA, Wherrett JR, Logan WJ (1993) Mitochondrial encephalomyopathy, lactic acidosis, stroke-like episodes (MELAS): clinical, radiological, pathological, and genetic observations. Ann Neurol 34:25–32
Moraes CT, Ciacci F, Silvestri G, Shanske S, Sciacco M, Schon EA, Bonilla E, DiMauaro S (1993) Atypical clinical presentations associated with the MELAS mutation at position 3243 of human mitochondrial DDNA. Neuromusc Disord 3:43–50
Oka Y, Katagiri H, Yazaki Y, Murase T, Kobayashi T (1993) Mitochondrial gene mutation in islet-cell-antibody-positive patients who were initially non-insulin-dependent diabetics. Lancet 342:527–528
Shanske A, Shanske S, Silvestri G, Miranda AF, Wertheim D, Lipper S, Chenys A (1992) MELAS point mutation with unusual clinical presentation. Neurology 42[Suppl 3]:268
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Kamakura, K., Abe, H., Tadano, Y. et al. Recurrent respiratory failure in a patient with 3243 mutation in mitochondrial DNA. J Neurol 242, 253–255 (1995). https://doi.org/10.1007/BF00919602
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DOI: https://doi.org/10.1007/BF00919602