164 related articles for article (PubMed ID: 521828)
1. 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]
2. Mitochondrial myopathy. Biochemical studies revealing a deficiency of NADH--cytochrome b reductase activity.
Land JM; Morgan-Hughes JA; Clark JB
J Neurol Sci; 1981 Apr; 50(1):1-13. PubMed ID: 7229653
[TBL] [Abstract][Full Text] [Related]
3. 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
[TBL] [Abstract][Full Text] [Related]
4. Mitochondrial myopathy and encephalopathy: three cases--a deficiency of NADH-CoQ dehydrogenase?
Holliday PL; Climie AR; Gilroy J; Mahmud MZ
Neurology; 1983 Dec; 33(12):1619-22. PubMed ID: 6417559
[TBL] [Abstract][Full Text] [Related]
5. Deficiency in ubiquinone cytochrome c reductase in a patient with mitochondrial myopathy and lactic acidosis.
Darley-Usmar VM; Kennaway NG; Buist NR; Capaldi RA
Proc Natl Acad Sci U S A; 1983 Aug; 80(16):5103-6. PubMed ID: 6308671
[TBL] [Abstract][Full Text] [Related]
6. NADH-CoQ reductase deficient myopathy: successful treatment with riboflavin.
Arts WF; Scholte HR; Bogaard JM; Kerrebijn KF; Luyt-Houwen IE
Lancet; 1983 Sep; 2(8349):581-2. PubMed ID: 6136740
[No Abstract] [Full Text] [Related]
7. Deficiency of the iron-sulfur clusters of mitochondrial reduced nicotinamide-adenine dinucleotide-ubiquinone oxidoreductase (complex I) in an infant with congenital lactic acidosis.
Moreadith RW; Batshaw ML; Ohnishi T; Kerr D; Knox B; Jackson D; Hruban R; Olson J; Reynafarje B; Lehninger AL
J Clin Invest; 1984 Sep; 74(3):685-97. PubMed ID: 6432847
[TBL] [Abstract][Full Text] [Related]
8. Two cases of NADH-coenzyme Q reductase deficiency: relationship to MELAS syndrome.
Kobayashi M; Morishita H; Sugiyama N; Yokochi K; Nakano M; Wada Y; Hotta Y; Terauchi A; Nonaka I
J Pediatr; 1987 Feb; 110(2):223-7. PubMed ID: 3100753
[TBL] [Abstract][Full Text] [Related]
9. 31P NMR examination of two patients with NADH-CoQ reductase deficiency.
Radda GK; Bore PJ; Gadian DG; Ross BD; Styles P; Taylor DJ; Morgan-Hughes J
Nature; 1982 Feb; 295(5850):608-9. PubMed ID: 6799841
[No Abstract] [Full Text] [Related]
10. Mitochondrial myopathies: deficiencies localized to complex I and complex III of the mitochondrial respiratory chain.
Morgan-Hughes JA; Hayes DJ; Cooper M; Clark JB
Biochem Soc Trans; 1985 Aug; 13(4):648-50. PubMed ID: 2993076
[No Abstract] [Full Text] [Related]
11. 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]
12. 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]
13. Human mitochondrial respiratory chain deficiencies.
Morgan-Hughes JA; Schapira AH; Cooper JM; Hayes DJ; Clark JB
Aust Paediatr J; 1988; 24 Suppl 1():55-7. PubMed ID: 2849394
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Deficiency of the reduced nicotinamide adenine dinucleotide dehydrogenase component of complex I of mitochondrial electron transport. Fatal infantile lactic acidosis and hypermetabolism with skeletal-cardiac myopathy and encephalopathy.
Hoppel CL; Kerr DS; Dahms B; Roessmann U
J Clin Invest; 1987 Jul; 80(1):71-7. PubMed ID: 3110216
[TBL] [Abstract][Full Text] [Related]
16. [Muscle pathology in mitochondrial myopathy].
Nonaka I
No To Hattatsu; 1987 Mar; 19(2):110-7. PubMed ID: 3030377
[No Abstract] [Full Text] [Related]
17. Extensive defects of mitochondrial electron-transfer chain in muscular cytochrome c oxidase deficiency.
Tanaka M; Miyabayashi S; Nishikimi M; Suzuki H; Shimomura Y; Ito K; Narisawa K; Tada K; Ozawa T
Pediatr Res; 1988 Oct; 24(4):447-54. PubMed ID: 2845344
[TBL] [Abstract][Full Text] [Related]
18. [Complex I (NADH coenzyme-Q-reductase) deficiency, MELAS syndrome and hypertrophic cardiomyopathy].
Márquez C; Bautista J; Arenas J; Segura D; Chinchón I; Rafel E; Campos Y; Huerta R
Neurologia; 1991 May; 6(5):185-7. PubMed ID: 1908255
[TBL] [Abstract][Full Text] [Related]
19. Mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes syndrome and NADH-CoQ reductase deficiency.
Kobayashi M; Morishita H; Sugiyama N; Yokochi K; Nakano M; Wada Y; Hotta Y; Terauchi A; Nonaka I
J Inherit Metab Dis; 1986; 9(3):301-4. PubMed ID: 3099078
[No Abstract] [Full Text] [Related]
20. [Ultrastructural immunocytochemical localization of electron-transport enzymes in mitochondrial myopathy].
Song DL; Sato T; Ujike H; Nonaka I; Ozawa T
Rinsho Shinkeigaku; 1989 Apr; 29(4):405-10. PubMed ID: 2558830
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]