Similar articles

• Histochemical, ultrastructural and biochemical study of muscle mitochondria in Leber's hereditary optic atrophy.

  Federico A, Manneschi L, Meloni M, Alessandrini C, Bardelli AM, Dotti MT, Sabatelli P. Federico A, et al. J Inherit Metab Dis. 1988;11 Suppl 2:193-7. doi: 10.1007/BF01804233. J Inherit Metab Dis. 1988. PMID: 2846962 No abstract available.
• Myoclonus epilepsy with ragged red fibers and multiple mtDNA deletions.

  Blumenthal DT, Shanske S, Schochet SS, Santorelli FM, DiMauro S, Jaynesm M, Bodensteiner J. Blumenthal DT, et al. Neurology. 1998 Feb;50(2):524-5. doi: 10.1212/wnl.50.2.524. Neurology. 1998. PMID: 9484389
• Partial cytochrome oxidase (aa3) deficiency in chronic progressive external ophthalmoplegia. Histochemical and biochemical studies.

  Byrne E, Dennett X, Trounce I, Henderson R. Byrne E, et al. J Neurol Sci. 1985 Dec;71(2-3):257-71. doi: 10.1016/0022-510x(85)90064-4. J Neurol Sci. 1985. PMID: 2418159
• On the stability of key enzymes of energy metabolism in muscle biopsies.

  Pache T, Reichmann H. Pache T, et al. Enzyme. 1990;43(4):183-7. doi: 10.1159/000468729. Enzyme. 1990. PMID: 1966286
• Defects of oxidative phosphorylation in man.

  Taylor RW, Birch-Machin MA, Lowerson S, Sherratt HS, West IC, Bartlett K, Turnbull DM. Taylor RW, et al. Biochem Soc Trans. 1993 Aug;21 ( Pt 3)(3):804-7. doi: 10.1042/bst0210804. Biochem Soc Trans. 1993. PMID: 8224514 Review. No abstract available.