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Journal Abstract Search
143 related items for PubMed ID: 2859691
1. Mitochondrial myopathy with diffuse activation and focal deficiency of mitochondrial ATPase and carnitine deficiency. Müller-Höcker J, Paetzke I, Pongratz D, Hübner G. Virchows Arch B Cell Pathol Incl Mol Pathol; 1985; 48(2):185-96. PubMed ID: 2859691 [Abstract] [Full Text] [Related]
2. 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 [Abstract] [Full Text] [Related]
15. Lactic acidosis and mitochondrial myopathy associated with deficiency of several components of complex III of the respiratory chain. Kennaway NG, Buist NR, Darley-Usmar VM, Papadimitriou A, Dimauro S, Kelley RI, Capaldi RA, Blank NK, D'Agostino A. Pediatr Res; 1984 Oct; 18(10):991-9. PubMed ID: 6093035 [Abstract] [Full Text] [Related]
16. Carnitine deficiency of skeletal muscle: report of a treated case. Angelini C, Lücke S, Cantarutti F. Neurology; 1976 Jul; 26(7):633-7. PubMed ID: 945511 [Abstract] [Full Text] [Related]
17. Follow-up study of a myopathy with loosely coupled mitochondria. Meijer AE, van Wijngaarden GK. Pathol Res Pract; 1983 Aug; 178(1):73-7. PubMed ID: 6227873 [Abstract] [Full Text] [Related]
18. Primary systemic carnitine deficiency under successful therapy: clinical, biochemical, ultrahistochemical and renal clearance studies. von Petrykowski W, Ketelsen UP, Schmidt-Sommerfield E, Penn D, Sawicka E, Struck E, Lehnert W, Haap K, Strassburg HM. Clin Neuropathol; 1985 Aug; 4(2):63-71. PubMed ID: 3995808 [Abstract] [Full Text] [Related]
19. Ragged-red fibers. A biochemical and morphological study. Black JT, Judge D, Demers L, Gordon S. J Neurol Sci; 1975 Dec; 26(4):479-88. PubMed ID: 128619 [Abstract] [Full Text] [Related]