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4. Mitochondrial cytochrome deficiency presenting as a myopathy with hypotonia, external ophthalmoplegia, and lactic acidosis in an infant and as fatal hepatopathy in a second cousin. Boustany RN; Aprille JR; Halperin J; Levy H; DeLong GR Ann Neurol; 1983 Oct; 14(4):462-70. PubMed ID: 6314875 [TBL] [Abstract][Full Text] [Related]
5. Chronic progressive external ophthalmoplegia with NADH-CoQ reductase deficiency: report of a case. Lee CC; Ko YM; Chen SS Zhonghua Yi Xue Za Zhi (Taipei); 1992 Jul; 50(1):77-82. PubMed ID: 1326393 [TBL] [Abstract][Full Text] [Related]
6. Focal deficiency of cytochrome c oxidase and of mitochondrial ATPase with histochemical evidence of loosely coupled oxidative phosphorylation in a mitochondrial myopathy of a patient with bilateral ptosis. An enzyme histochemical, immunocytochemical and fine structural study. Müller-Höcker J; Stünkel S; Pongratz D; Hübner G J Neurol Sci; 1985; 69(1-2):27-36. PubMed ID: 2989441 [TBL] [Abstract][Full Text] [Related]
7. Enzyme activity measured in single muscle fibers in partial cytochrome c oxidase deficiency. Reichmann H Neurology; 1988 Feb; 38(2):244-9. PubMed ID: 2829055 [TBL] [Abstract][Full Text] [Related]
8. Partial deficiency of complexes I and IV of the mitochondrial respiratory chain in skeletal muscle of two patients with mitochondrial myopathy. Bleistein J; Zierz S J Neurol; 1989 May; 236(4):218-22. PubMed ID: 2547913 [TBL] [Abstract][Full Text] [Related]
9. Focal deficiency of cytochrome-c-oxidase in skeletal muscle of patients with progressive external ophthalmoplegia. Cytochemical-fine-structural study. Müller-Höcker J; Pongratz D; Hübner G Virchows Arch A Pathol Anat Histopathol; 1983; 402(1):61-71. PubMed ID: 6318426 [TBL] [Abstract][Full Text] [Related]
10. Morphometric analysis of skeletal muscle fibres and capillaries in mitochondrial myopathies. Scelsi R Pathol Res Pract; 1992 Jun; 188(4-5):607-11. PubMed ID: 1329053 [TBL] [Abstract][Full Text] [Related]
11. Endocrine involvement in mitochondrial encephalomyopathy with partial cytochrome c oxidase deficiency. Doriguzzi C; Palmucci L; Mongini T; Bresolin N; Bet L; Comi G; Lala R J Neurol Neurosurg Psychiatry; 1989 Jan; 52(1):122-5. PubMed ID: 2540284 [TBL] [Abstract][Full Text] [Related]
12. Enzyme activity analyses along ragged-red and normal single muscle fibres. Reichmann H Histochemistry; 1992 Sep; 98(2):131-4. PubMed ID: 1330995 [TBL] [Abstract][Full Text] [Related]
13. Mitochondrial myopathies: divergences of genetic deletions, biochemical defects and the clinical syndromes. Gerbitz KD; Obermaier-Kusser B; Zierz S; Pongratz D; Müller-Höcker J; Lestienne P J Neurol; 1990 Feb; 237(1):5-10. PubMed ID: 2156958 [TBL] [Abstract][Full Text] [Related]
14. Contrasting histochemical features of various mitochondrial syndromes. Collins S; Byrne E; Dennett X Acta Neurol Scand; 1995 Apr; 91(4):287-93. PubMed ID: 7625156 [TBL] [Abstract][Full Text] [Related]
15. Ragged red or ragged blue fibers. Reichmann H; Vogler L; Seibel P Eur Neurol; 1996; 36(2):98-102. PubMed ID: 8654494 [TBL] [Abstract][Full Text] [Related]
16. Mitochondrial genome distribution in histochemically cytochrome c oxidase-negative muscle fibres in patients with a mixture of deleted and wild type mitochondrial DNA. Collins S; Rudduck C; Marzuki S; Dennett X; Byrne E Biochim Biophys Acta; 1991 Nov; 1097(4):309-17. PubMed ID: 1660306 [TBL] [Abstract][Full Text] [Related]
17. Mitochondrial encephalomyopathy and partial cytochrome c oxidase deficiency. Servidei S; Lazaro RP; Bonilla E; Barron KD; Zeviani M; DiMauro S Neurology; 1987 Jan; 37(1):58-63. PubMed ID: 3025775 [TBL] [Abstract][Full Text] [Related]