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9. [Myopathy due to succinate cytochrome C oxidoreductase deficiency: possible defect of complex II of the respiratory chain]. Werneck LC; DiMauro S Arq Neuropsiquiatr; 1989 Dec; 47(4):461-7. PubMed ID: 2561340 [TBL] [Abstract][Full Text] [Related]
10. Fatal lipid storage myopathy with deficiency of cytochrome-c-oxidase and carnitine. A contribution to the combined cytochemical-finestructural identification of cytochrome-c-oxidase in longterm frozen muscle. Müller-Höcker J; Pongratz D; Deufel T; Trijbels JM; Endres W; Hübner G Virchows Arch A Pathol Anat Histopathol; 1983; 399(1):11-23. PubMed ID: 6298999 [TBL] [Abstract][Full Text] [Related]
11. Carnitine deficiency: clinical, morphological, and biochemical observations in a fatal case. Engel AG; Banker BQ; Eiben RM J Neurol Neurosurg Psychiatry; 1977 Apr; 40(4):313-22. PubMed ID: 874508 [TBL] [Abstract][Full Text] [Related]
12. A mitochondrial myopathy with a deficiency of respiratory chain NADH-CoQ reductase activity. Morgan-Hughes JA; Darveniza P; Landon DN; Land JM; Clark JB J Neurol Sci; 1979 Sep; 43(1):27-46. PubMed ID: 521828 [TBL] [Abstract][Full Text] [Related]
13. [A case of MELAS (mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes) with progressive cytochrome c oxidase deficiency]. Sumi K; Nagaura T; Itagaki Y; Inui K; Abe J Rinsho Shinkeigaku; 1989 Jul; 29(7):901-8. PubMed ID: 2553313 [TBL] [Abstract][Full Text] [Related]
14. 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 [TBL] [Abstract][Full Text] [Related]
15. Mitochondrial myopathies: disorders of the respiratory chain and oxidative phosphorylation. Clark JB; Hayes DJ; Morgan-Hughes JA; Byrne E J Inherit Metab Dis; 1984; 7 Suppl 1():62-8. PubMed ID: 6434847 [TBL] [Abstract][Full Text] [Related]
16. [Myopathy with carnitine deficiency and lactic acidosis. A contribution to differential diagnosis of carnitine deficiency myopathies and mitochondrial myopathies]. Cammann R; Dunker H; Schumacher H; Ruitenbeek W; Sperner J Z Arztl Fortbild (Jena); 1992 Jul; 86(13):667-71. PubMed ID: 1642019 [No Abstract] [Full Text] [Related]
17. A case of mitochondrial myopathy, lactic acidosis and complex I deficiency. Bet L; Bresolin N; Moggio M; Meola G; Prelle A; Schapira AH; Binzoni T; Chomyn A; Fortunato F; Cerretelli P J Neurol; 1990 Nov; 237(7):399-404. PubMed ID: 2125637 [TBL] [Abstract][Full Text] [Related]
18. Carnitine deficiency. Răşanu T; Mehedinţi-Hâncu M; Alexianu M; Mehedinţi T; Gheorghe E; Damian I Rom J Morphol Embryol; 2012; 53(1):203-6. PubMed ID: 22395524 [TBL] [Abstract][Full Text] [Related]