149 related articles for article (PubMed ID: 4050316)
1. Subacute necrotizing encephalomyelopathy (Leigh syndrome) associated with disturbed oxidation of pyruvate, malate and 2-oxoglutarate in muscle and liver.
Van Erven PM; Gabreëls FJ; Ruitenbeek W; Den Hartog MR; Fischer JC; Renier WO; Trijbels JM; Slooff JL; Janssen AJ
Acta Neurol Scand; 1985 Jul; 72(1):36-42. PubMed ID: 4050316
[TBL] [Abstract][Full Text] [Related]
2. Disturbed oxidative metabolism in subacute necrotizing encephalomyelopathy (Leigh syndrome).
van Erven PM; Ruitenbeek W; Gabreëls FJ; Renier WO; Fischer JC; Janssen AJ
Neuropediatrics; 1986 Feb; 17(1):28-32. PubMed ID: 3008021
[TBL] [Abstract][Full Text] [Related]
3. Cytochrome c oxidase deficiency in subacute necrotizing encephalomyelopathy.
Arts WF; Scholte HR; Loonen MC; Przyrembel H; Fernandes J; Trijbels JM; Luyt-Houwen IE
J Neurol Sci; 1987 Jan; 77(1):103-15. PubMed ID: 3027266
[TBL] [Abstract][Full Text] [Related]
4. Familial Leigh's syndrome: association with a defect in oxidative metabolism probably restricted to brain.
van Erven PM; Gabreëls FJ; Ruitenbeek W; Renier WO; Lamers KJ; Sloof JL
J Neurol; 1987 May; 234(4):215-9. PubMed ID: 3612192
[TBL] [Abstract][Full Text] [Related]
5. Cytochrome C oxidase deficiency in two siblings with Leigh encephalomyelopathy.
Miyabayashi S; Narisawa K; Iinuma K; Tada K; Sakai K; Kobayashi K; Kobayashi Y; Morinaga S
Brain Dev; 1984; 6(4):362-72. PubMed ID: 6093613
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Pyruvate dehydrogenase activity is not deficient in the brain of three autopsied cases with Leigh disease (subacute necrotizing encephalomyelopathy, SNE).
Kustermann-Kuhn B; Harzer K; Schröder R; Permanetter W; Peiffer J
Hum Genet; 1984; 68(1):51-3. PubMed ID: 6437963
[TBL] [Abstract][Full Text] [Related]
8. Cytochrome c oxidase deficiency in Leigh syndrome.
DiMauro S; Servidei S; Zeviani M; DiRocco M; DeVivo DC; DiDonato S; Uziel G; Berry K; Hoganson G; Johnsen SD
Ann Neurol; 1987 Oct; 22(4):498-506. PubMed ID: 2829705
[TBL] [Abstract][Full Text] [Related]
9. Gluconeogenesis in guinea pig renal tubule fragments--effects of noradrenaline, 3':5' cyclic AMP and angiotensin II.
Veiga JA; Saggerson ED
Comp Biochem Physiol C Comp Pharmacol Toxicol; 1983; 74(2):409-12. PubMed ID: 6133691
[TBL] [Abstract][Full Text] [Related]
10. [Leigh's subacute necrotizing encephalomyelopathy due to decreased activity of the pyruvate dehydrogenase complex].
Siemes H; Goebel HH; Sengers RC; Ruitenbeek W; Trijbels JM
Monatsschr Kinderheilkd; 1987 Dec; 135(12):821-6. PubMed ID: 3125426
[TBL] [Abstract][Full Text] [Related]
11. The control of tricarboxylate-cycle oxidations in blowfly flight muscle. The steady-state concentrations of citrate, isocitrate 2-oxoglutarate and malate in flight muscle and isolated mitochondria.
Johnson RN; Hansford RG
Biochem J; 1975 Mar; 146(3):527-35. PubMed ID: 1147907
[TBL] [Abstract][Full Text] [Related]
12. Rescue from galactose-induced death of Leigh Syndrome patient cells by pyruvate and NAD
Iannetti EF; Smeitink JAM; Willems PHGM; Beyrath J; Koopman WJH
Cell Death Dis; 2018 Nov; 9(11):1135. PubMed ID: 30429455
[TBL] [Abstract][Full Text] [Related]
13. Immunochemical study in three patients with cytochrome c oxidase deficiency presenting Leigh's encephalomyelopathy.
Miyabayashi S; Ito T; Abukawa D; Narisawa K; Tada K; Tanaka M; Ozawa T; Droste M; Kadenbach B
J Inherit Metab Dis; 1987; 10(3):289-92. PubMed ID: 2828763
[No Abstract] [Full Text] [Related]
14. de Toni-Fanconi-Debré syndrome with Leigh syndrome revealing severe muscle cytochrome c oxidase deficiency.
Ogier H; Lombes A; Scholte HR; Poll-The BT; Fardeau M; Alcardi J; Vignes B; Niaudet P; Saudubray JM
J Pediatr; 1988 May; 112(5):734-9. PubMed ID: 2834526
[TBL] [Abstract][Full Text] [Related]
15. [Subacute necrotizing encephalopathy, Leigh's disease. Apropos of a case].
Delisle MB; Netter JC; Peyrille F; Bouissou H
Ann Pathol; 1985; 5(4-5):313-7. PubMed ID: 3833250
[TBL] [Abstract][Full Text] [Related]
16. Neonatal cardiomyopathy and lactic acidosis responsive to thiamine.
Bakker HD; Scholte HR; Luyt-Houwen IE; van Gennip AH; Abeling NG; Lam J
J Inherit Metab Dis; 1991; 14(1):75-9. PubMed ID: 1861462
[TBL] [Abstract][Full Text] [Related]
17. [The role of malate in regulating the rate of mitochondrial respiration in vitro].
Vovyleva-Guarriero VB; Wehbie RS; Muscatello U; Lardi GA
Biokhimiia; 1991 Mar; 56(3):542-51. PubMed ID: 1883909
[TBL] [Abstract][Full Text] [Related]
18. Mitochondrial abnormalities in choroid plexus of Leigh disease.
Ohama E; Ikuta F; Nakamura N
Brain Dev; 1988; 10(1):30-5. PubMed ID: 3285724
[TBL] [Abstract][Full Text] [Related]
19. Region-Specific Defects of Respiratory Capacities in the Ndufs4(KO) Mouse Brain.
Kayser EB; Sedensky MM; Morgan PG
PLoS One; 2016; 11(1):e0148219. PubMed ID: 26824698
[TBL] [Abstract][Full Text] [Related]
20. Normal activities of hepatic pyruvate dehydrogenase and pyruvate carboxylase in Leigh's syndrome.
Tsuchiyama A; Oyanagi K; Sogawa H; Nakao T; Ogawa K; Fujita S
Tohoku J Exp Med; 1983 Jan; 139(1):67-72. PubMed ID: 6836560
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
