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4. [A case of mitochondrial encephalomyopathy with a defect in electron transport at complex I and IV in skeletal muscle showing peripheral neuropathy]. Ohnishi A; Nakano S; Hashimoto T; Tsuji S; Murai Y Rinsho Shinkeigaku; 1988 Jan; 28(1):107-11. PubMed ID: 2838209 [No Abstract] [Full Text] [Related]
6. [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]
7. Mitochondrial encephalomyopathies: a correlation between neuropathological findings and defects in mitochondrial DNA. McKelvie PA; Morley JB; Byrne E; Marzuki S J Neurol Sci; 1991 Mar; 102(1):51-60. PubMed ID: 1906931 [TBL] [Abstract][Full Text] [Related]
8. [The mitochondrial genome and its relation to human pathology]. López de Munain A; Martí-Massó JF Neurologia; 1991; 6(7):251-5. PubMed ID: 1768444 [No Abstract] [Full Text] [Related]
9. [Mitochondrial encephalomyopathies. A comparison of Kearns-Sayre syndrome, MELAS and MERRF]. Zenner K; Gold R; Meurers B; Reichmann H Nervenarzt; 1990 Oct; 61(10):597-603. PubMed ID: 2177152 [No Abstract] [Full Text] [Related]
10. Benign mitochondrial myopathy with deficiency of NADH-CoQ reductase and cytochrome c oxidase. Roodhooft AM; Van Acker KJ; Martin JJ; Ceuterick C; Scholte HR; Luyt-Houwen IE Neuropediatrics; 1986 Nov; 17(4):221-6. PubMed ID: 3027606 [TBL] [Abstract][Full Text] [Related]
11. Partial deficiency of subunits in complex I or IV of patients with mitochondrial myopathies. Tanaka M; Nishikimi M; Suzuki H; Ozawa T; Koga Y; Nonaka I Biochem Int; 1987 Mar; 14(3):525-30. PubMed ID: 2884999 [TBL] [Abstract][Full Text] [Related]
12. The mitochondrial myopathies. Defects of the mitochondrial respiratory chain and oxidative phosphorylation system. Morgan-Hughes JA; Cooper JM; Schapira AH; Hayes DJ; Clark JB Electroencephalogr Clin Neurophysiol Suppl; 1987; 39():103-14. PubMed ID: 2888641 [No 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]
15. [Retinitis pigmentosa in Kearns-Sayre syndrome resulting from mutation of mitochondrial DNA "de novo"]. Midro AT; Zalewska R; Skrzypczak-Adamiak G; Wilichowski E Klin Oczna; 1995 Jun; 97(6):203-6. PubMed ID: 7643565 [TBL] [Abstract][Full Text] [Related]
16. [31P-NMR spectroscopy of mitochondrial myopathies: the relation between abnormal energy metabolism and muscle biopsy findings]. Kawai M; Itoh M; Okazawa H; Kamakura K Rinsho Shinkeigaku; 1989 Feb; 29(2):167-71. PubMed ID: 2546706 [TBL] [Abstract][Full Text] [Related]
17. [Kearns-Sayre and Melas syndromes]. Zammarchi E Minerva Pediatr; 1991 Mar; 43(3):111-3. PubMed ID: 1870504 [No Abstract] [Full Text] [Related]
18. [Clinical aspects of mitochondrial encephalomyopathy--abnormality of mitochondrial respiratory chain]. Nakagawa M; Osame M No To Shinkei; 1990 Aug; 42(8):719-33. PubMed ID: 2121197 [No Abstract] [Full Text] [Related]
19. Spontaneous Kearns-Sayre/chronic external ophthalmoplegia plus syndrome associated with a mitochondrial DNA deletion: a slip-replication model and metabolic therapy. Shoffner JM; Lott MT; Voljavec AS; Soueidan SA; Costigan DA; Wallace DC Proc Natl Acad Sci U S A; 1989 Oct; 86(20):7952-6. PubMed ID: 2554297 [TBL] [Abstract][Full Text] [Related]