These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
107 related articles for article (PubMed ID: 2854407)
1. Clinical and biochemical studies on cytochrome oxidase deficiencies. Schon EA; Bonilla E; Lombes A; Moraes CT; Nakase H; Rizzuto R; Zeviani M; DiMauro S Ann N Y Acad Sci; 1988; 550():348-59. PubMed ID: 2854407 [No Abstract] [Full Text] [Related]
2. Molecular defects in cytochrome oxidase in mitochondrial diseases. DiMauro S; Zeviani M; Rizzuto R; Lombes A; Nakase H; Bonilla E; Miranda A; Schon E J Bioenerg Biomembr; 1988 Jun; 20(3):353-64. PubMed ID: 2841309 [TBL] [Abstract][Full Text] [Related]
3. Cytochrome c oxidase deficiency. DiMauro S; Lombes A; Nakase H; Mita S; Fabrizi GM; Tritschler HJ; Bonilla E; Miranda AF; DeVivo DC; Schon EA Pediatr Res; 1990 Nov; 28(5):536-41. PubMed ID: 2175026 [TBL] [Abstract][Full Text] [Related]
4. Cytochrome oxidase deficiency: clinical and biochemical heterogeneity. DiMauro S; Zeviani M; Servidei S; Bonilla E; Miranda AF; Prelle A; Schon EA Ann N Y Acad Sci; 1986; 488():19-32. PubMed ID: 3034115 [No Abstract] [Full Text] [Related]
5. Biochemical and molecular aspects of cytochrome C oxidase deficiency. DiMauro S; Zeviani M; Servidei S; Prelle A; Miranda AF; Bonilla E; Schon EA Adv Neurol; 1988; 48():93-105. PubMed ID: 2825476 [No Abstract] [Full Text] [Related]
6. Mitochondrial encephalomyopathies: biochemical approach. Dimauro S; Moraes CT; Shanske S; Lombes A; Nakase H; Mita S; Tritschler HJ; Bonilla E; Miranda AF; Schon EA Rev Neurol (Paris); 1991; 147(6-7):443-9. PubMed ID: 1660180 [TBL] [Abstract][Full Text] [Related]
7. [Mitochondrial encephalomyopathy]. Scarlato G; Bresolin N; Moggio M; Bet L; Meola G Recenti Prog Med; 1989 Dec; 80(12):665-72. PubMed ID: 2560839 [TBL] [Abstract][Full Text] [Related]
8. Mutations of mitochondrial DNA and human death. Kadenbach B; Müller-Höcker J Naturwissenschaften; 1990 May; 77(5):221-5. PubMed ID: 2165572 [TBL] [Abstract][Full Text] [Related]
9. Cytochrome c oxidase deficiency. DiMauro S; Zeviani M; Bonilla E; Bresolin N; Nakagawa M; Miranda AF; Moggio M Biochem Soc Trans; 1985 Aug; 13(4):651-3. PubMed ID: 2993077 [No Abstract] [Full Text] [Related]
10. Maternal inheritance of deleted mitochondrial DNA in a family with mitochondrial myopathy. Ozawa T; Yoneda M; Tanaka M; Ohno K; Sato W; Suzuki H; Nishikimi M; Yamamoto M; Nonaka I; Horai S Biochem Biophys Res Commun; 1988 Aug; 154(3):1240-7. PubMed ID: 2841928 [TBL] [Abstract][Full Text] [Related]
11. Defects in the cytochrome bc1 complex in mitochondrial diseases. Kennaway NG J Bioenerg Biomembr; 1988 Jun; 20(3):325-52. PubMed ID: 2841308 [TBL] [Abstract][Full Text] [Related]
12. Differential diagnosis of fatal and benign cytochrome c oxidase-deficient myopathies of infancy: an immunohistochemical approach. Tritschler HJ; Bonilla E; Lombes A; Andreetta F; Servidei S; Schneyder B; Miranda AF; Schon EA; Kadenbach B; DiMauro S Neurology; 1991 Feb; 41(2 ( Pt 1)):300-5. PubMed ID: 1846953 [TBL] [Abstract][Full Text] [Related]
13. Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS): a correlative study of the clinical features and mitochondrial DNA mutation. Goto Y; Horai S; Matsuoka T; Koga Y; Nihei K; Kobayashi M; Nonaka I Neurology; 1992 Mar; 42(3 Pt 1):545-50. PubMed ID: 1549215 [TBL] [Abstract][Full Text] [Related]
14. Cytochrome c oxidase deficiency. Comi GP; Strazzer S; Galbiati S; Bresolin N Int Rev Neurobiol; 2002; 53():205-40. PubMed ID: 12512342 [No Abstract] [Full Text] [Related]
15. Detection of "deleted" mitochondrial genomes in cytochrome-c oxidase-deficient muscle fibers of a patient with Kearns-Sayre syndrome. Mita S; Schmidt B; Schon EA; DiMauro S; Bonilla E Proc Natl Acad Sci U S A; 1989 Dec; 86(23):9509-13. PubMed ID: 2556715 [TBL] [Abstract][Full Text] [Related]
17. Fatal infantile mitochondrial cardiomyopathy and myopathy with heterogeneous tissue expression of combined respiratory chain deficiencies. Müller-Höcker J; Ibel H; Paetzke I; Deufel T; Endres W; Kadenbach B; Gokel JM; Hübner G Virchows Arch A Pathol Anat Histopathol; 1991; 419(4):355-62. PubMed ID: 1659034 [TBL] [Abstract][Full Text] [Related]
18. Human mitochondrial complex I dysfunction. Cooper JM; Mann VM; Krige D; Schapira AH Biochim Biophys Acta; 1992 Jul; 1101(2):198-203. PubMed ID: 1633185 [TBL] [Abstract][Full Text] [Related]
19. Immunocytochemical studies of cytochrome oxidase subunits in skeletal muscle of patients with partial cytochrome oxidase deficiencies. Johnson MA; Kadenbach B; Droste M; Old SL; Turnbull DM J Neurol Sci; 1988 Oct; 87(1):75-90. PubMed ID: 2848095 [TBL] [Abstract][Full Text] [Related]
20. A case of mitochondrial myopathy, encephalopathy and lactic acidosis due to cytochrome c oxidase deficiency with neurogenic muscular changes. Jinnai K; Yamada H; Kanda F; Masui Y; Tanaka M; Ozawa T; Fujita T Eur Neurol; 1990; 30(1):56-60. PubMed ID: 2153548 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]