Similar articles

• Mitochondrial myopathies. Clinical, morphological and biochemical aspects.

  Sengers RC, Stadhouders AM, Trijbels JM. Sengers RC, et al. Eur J Pediatr. 1984 Feb;141(4):192-207. doi: 10.1007/BF00572761. Eur J Pediatr. 1984. PMID: 6329761 Review. No abstract available.
• [Neurological approach to mitochondrial abnormalities].

  Yokochi K. Yokochi K. No To Hattatsu. 1987 Mar;19(2):118-24. No To Hattatsu. 1987. PMID: 3030378 Japanese. No abstract available.
• Benign mitochondrial myopathy with deficiency of NADH-CoQ reductase and cytochrome c oxidase.

  Roodhooft AM, Van Acker KJ, Martin JJ, Ceuterick C, Scholte HR, Luyt-Houwen IE. Roodhooft AM, et al. Neuropediatrics. 1986 Nov;17(4):221-6. doi: 10.1055/s-2008-1052534. Neuropediatrics. 1986. PMID: 3027606
• Mitochondrial myopathy and encephalopathy: three cases--a deficiency of NADH-CoQ dehydrogenase?

  Holliday PL, Climie AR, Gilroy J, Mahmud MZ. Holliday PL, et al. Neurology. 1983 Dec;33(12):1619-22. doi: 10.1212/wnl.33.12.1619. Neurology. 1983. PMID: 6417559
• Human mitochondrial respiratory chain deficiencies.

  Morgan-Hughes JA, Schapira AH, Cooper JM, Hayes DJ, Clark JB. Morgan-Hughes JA, et al. Aust Paediatr J. 1988;24 Suppl 1:55-7. Aust Paediatr J. 1988. PMID: 2849394 Review.