144 related articles for article (PubMed ID: 10445463)
1. Uncommon morphologic characteristics in Leigh's disease.
Warmuth-Metz M; Hofmann E; Büsse M; Solymosi L
AJNR Am J Neuroradiol; 1999; 20(6):1158-60. PubMed ID: 10445463
[TBL] [Abstract][Full Text] [Related]
2. Proton spectroscopy in five patients with Leigh's disease and mitochondrial enzyme deficiency.
Krägeloh-Mann I; Grodd W; Schöning M; Marquard K; Nägele T; Ruitenbeek W
Dev Med Child Neurol; 1993 Sep; 35(9):769-76. PubMed ID: 7689066
[TBL] [Abstract][Full Text] [Related]
3. [Metabolic study in a child with Leigh's syndrome and deficient activity in complex I of the respiratory chain].
Zeman J; Klement P; Houst'ková H; Hrebícek M; Hansíková H; Richterová I; Velenská Z; Houstĕk J
Cesk Pediatr; 1993 Oct; 48(10):586-9. PubMed ID: 8269530
[TBL] [Abstract][Full Text] [Related]
4. Systems analysis of energy metabolism elucidates the affected respiratory chain complex in Leigh's syndrome.
Vo TD; Paul Lee WN; Palsson BO
Mol Genet Metab; 2007 May; 91(1):15-22. PubMed ID: 17336115
[TBL] [Abstract][Full Text] [Related]
5. Coenzyme Q10 levels correlate with the activities of complexes I and II/III in mitochondria from parkinsonian and nonparkinsonian subjects.
Shults CW; Haas RH; Passov D; Beal MF
Ann Neurol; 1997 Aug; 42(2):261-4. PubMed ID: 9266740
[TBL] [Abstract][Full Text] [Related]
6. Deficiency of pyruvate dehydrogenase complex (PDHC) in Leigh's disease fibroblasts: an abnormality in lipoamide dehydrogenase affecting PDHC activation.
Hinman LM; Sheu KF; Baker AC; Kim YT; Blass JP
Neurology; 1989 Jan; 39(1):70-5. PubMed ID: 2909916
[TBL] [Abstract][Full Text] [Related]
7. Consequences of aging on mitochondrial respiratory chain enzymes in cultured human fibroblasts treated with ascorbate.
Sharma P; Rupar CA; Rip JW
Gerontology; 1998; 44(2):78-84. PubMed ID: 9523218
[TBL] [Abstract][Full Text] [Related]
8. Biochemical study in 28 children with lactic acidosis, in relation to Leigh's encephalomyelopathy.
Miyabayashi S; Ito T; Narisawa K; Iinuma K; Tada K
Eur J Pediatr; 1985 Mar; 143(4):278-83. PubMed ID: 2985393
[TBL] [Abstract][Full Text] [Related]
9. Similarities between mitochondrial and bacterial electron transport with particular reference to the action of inhibitors.
Ferguson SJ
Biochem Soc Trans; 1994 Feb; 22(1):181-3. PubMed ID: 8206221
[No Abstract] [Full Text] [Related]
10. Development of mitochondrial respiratory-chain complexes in neonatal rat brain.
Almeida A; Bates TE; Clark JB
Biochem Soc Trans; 1994 Nov; 22(4):409S. PubMed ID: 7698431
[No Abstract] [Full Text] [Related]
11. Proton spectroscopy in patients with Leigh's disease and mitochondrial enzyme deficiency.
Kruse B; Hanefeld F; Holzbach U; Wilichowski E; Christen HJ; Merboldt KD; Hänicke W; Frahm J
Dev Med Child Neurol; 1994 Sep; 36(9):839-43. PubMed ID: 7926334
[No Abstract] [Full Text] [Related]
12. Mitochondrial myopathy with succinate dehydrogenase and aconitase deficiency. Abnormalities of several iron-sulfur proteins.
Hall RE; Henriksson KG; Lewis SF; Haller RG; Kennaway NG
J Clin Invest; 1993 Dec; 92(6):2660-6. PubMed ID: 8254022
[TBL] [Abstract][Full Text] [Related]
13. Low platelet mitochondrial complex I and complex II/III activity in early untreated Parkinson's disease.
Haas RH; Nasirian F; Nakano K; Ward D; Pay M; Hill R; Shults CW
Ann Neurol; 1995 Jun; 37(6):714-22. PubMed ID: 7778844
[TBL] [Abstract][Full Text] [Related]
14. Impaired energy metabolism in hearts of septic baboons: diminished activities of Complex I and Complex II of the mitochondrial respiratory chain.
Gellerich FN; Trumbeckaite S; Hertel K; Zierz S; Müller-Werdan U; Werdan K; Redl H; Schlag G
Shock; 1999 May; 11(5):336-41. PubMed ID: 10353539
[TBL] [Abstract][Full Text] [Related]
15. Mitochondrial electron transport chain defect presenting as hypoglycemia.
Freckmann ML; Thorburn DR; Kirby DM; Kamath KR; Hammond J; Dennett X; Christodoulou J
J Pediatr; 1997 Mar; 130(3):431-6. PubMed ID: 9063420
[TBL] [Abstract][Full Text] [Related]
16. Interaction of ubiquinone and vitamin K3 with mitochondrial succinate-ubiquinone oxidoreductase.
Kotlyar AB; Gutman M; Ackrell BA
Biochem Biophys Res Commun; 1992 Aug; 186(3):1656-62. PubMed ID: 1510689
[TBL] [Abstract][Full Text] [Related]
17. Direct interaction between mitochondrial succinate-ubiquinone and ubiquinol-cytochrome c oxidoreductases probed by sensitivity to quinone-related inhibitors.
Yamashita A; Miyoshi H; Hatano T; Iwamura H
J Biochem; 1996 Aug; 120(2):377-84. PubMed ID: 8889824
[TBL] [Abstract][Full Text] [Related]
18. Mitochondrial myopathy with a defect of mitochondrial-protein transport.
Schapira AH; Cooper JM; Morgan-Hughes JA; Landon DN; Clark JB
N Engl J Med; 1990 Jul; 323(1):37-42. PubMed ID: 2113185
[No Abstract] [Full Text] [Related]
19. Deficiency in complex II of the respiratory chain, presenting as a leukodystrophy in two sisters with Leigh syndrome.
Burgeois M; Goutieres F; Chretien D; Rustin P; Munnich A; Aicardi J
Brain Dev; 1992 Nov; 14(6):404-8. PubMed ID: 1492653
[TBL] [Abstract][Full Text] [Related]
20. [Complex II (succinate-ubiquinone reductase) deficiency].
Nonaka I
Ryoikibetsu Shokogun Shirizu; 2001; (36):132-4. PubMed ID: 11596343
[No Abstract] [Full Text] [Related]
[Next] [New Search]