95 related articles for article (PubMed ID: 9427157)
1. Mitochondrial respiratory chain succinate-cytochrome-c oxidoreductase deficiency and hepatic cirrhosis.
Sewell AC; Herwig J; Böhles HJ; Sperl W
J Inherit Metab Dis; 1997 Nov; 20(6):837-8. PubMed ID: 9427157
[No Abstract] [Full Text] [Related]
2. Cirrhosis in a child with deficiency of mitochondrial respiratory-chain succinate-cytochrome c-oxidoreductase.
Sewell AC; Sperl W; Herwig J; Böhles HJ
J Pediatr; 1997 Jul; 131(1 Pt 1):166-8. PubMed ID: 9255214
[No Abstract] [Full Text] [Related]
3. Mitochondrial myopathy with lactic acidosis and deficient activity of muscle succinate cytochrome-c-oxidoreductase.
Behbehani AW; Goebel H; Osse G; Gabriel M; Langenbeck U; Berden J; Berger R; Schutgens RB
Eur J Pediatr; 1984 Nov; 143(1):67-71. PubMed ID: 6096151
[TBL] [Abstract][Full Text] [Related]
4. [Myopathy due to succinate cytochrome C oxidoreductase deficiency: possible defect of complex II of the respiratory chain].
Werneck LC; DiMauro S
Arq Neuropsiquiatr; 1989 Dec; 47(4):461-7. PubMed ID: 2561340
[TBL] [Abstract][Full Text] [Related]
5. Fatal hepatic failure with lactic acidaemia, Fanconi syndrome and defective activity of succinate:cytochrome c reductase.
Vilaseca MA; Briones P; Ribes A; Carreras E; Llácer A; Querol J
J Inherit Metab Dis; 1991; 14(3):285-8. PubMed ID: 1663190
[No Abstract] [Full Text] [Related]
6. Cerebral white matter disease in children may be caused by mitochondrial respiratory chain deficiency.
de Lonlay-Debeney P; von Kleist-Retzow JC; Hertz-Pannier L; Peudenier S; Cormier-Daire V; Berquin P; Chrétien D; Rötig A; Saudubray JM; Baraton J; Brunelle F; Rustin P; Van Der Knaap M; Munnich A
J Pediatr; 2000 Feb; 136(2):209-14. PubMed ID: 10657827
[TBL] [Abstract][Full Text] [Related]
7. Human mitochondrial electron transport chain: assay of succinate: cytochrome c reductase in leukocytes, platelets and cultured fibroblasts.
Stumpf DA; Parks JK
Biochem Med; 1981 Apr; 25(2):234-8. PubMed ID: 6269538
[No Abstract] [Full Text] [Related]
8. Mitochondrial myopathy with lactic acidaemia, Fanconi-De Toni-Debré syndrome and a disturbed succinate: cytochrome c oxidoreductase activity.
Sperl W; Ruitenbeek W; Trijbels JM; Sengers RC; Stadhouders AM; Guggenbichler JP
Eur J Pediatr; 1988 May; 147(4):418-21. PubMed ID: 2840289
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. [Pure mitochondrial myopathy].
Murakami N; Sakuta R
Ryoikibetsu Shokogun Shirizu; 2001; (36):186-9. PubMed ID: 11596366
[No Abstract] [Full Text] [Related]
11. Defects of oxidative phosphorylation in man.
Taylor RW; Birch-Machin MA; Lowerson S; Sherratt HS; West IC; Bartlett K; Turnbull DM
Biochem Soc Trans; 1993 Aug; 21 ( Pt 3)(3):804-7. PubMed ID: 8224514
[No Abstract] [Full Text] [Related]
12. Evidence for the existence of a ubiquinone protein and its radical in the cytochromes b and c1 region in the mitochondrial electron transport chain.
Yu CA; Nagaoka S; Yu L; King TE
Biochem Biophys Res Commun; 1978 Jun; 82(4):1070-8. PubMed ID: 212034
[No Abstract] [Full Text] [Related]
13. Multiple sites of inhibition of mitochondrial electron transport by local anesthetics.
Chazotte B; Vanderkooi G
Biochim Biophys Acta; 1981 Jul; 636(2):153-61. PubMed ID: 6269599
[TBL] [Abstract][Full Text] [Related]
14. Fatal combined defects in mitochondrial multienzyme complexes in two siblings.
Robinson BH; Chow W; Petrova-Benedict R; Clarke JT; Van Allen MI; Becker LE; Boulton JE; Ragan I
Eur J Pediatr; 1992 May; 151(5):347-52. PubMed ID: 1327797
[TBL] [Abstract][Full Text] [Related]
15. Rett syndrome and mitochondrial enzyme deficiencies.
Coker SB; Melnyk AR
J Child Neurol; 1991 Apr; 6(2):164-6. PubMed ID: 1646255
[TBL] [Abstract][Full Text] [Related]
16. Differential inhibition by hyperammonemia of the electron transport chain enzymes in synaptosomes and non-synaptic mitochondria in ornithine transcarbamylase-deficient spf-mice: restoration by acetyl-L-carnitine.
Qureshi K; Rao KV; Qureshi IA
Neurochem Res; 1998 Jun; 23(6):855-61. PubMed ID: 9572674
[TBL] [Abstract][Full Text] [Related]
17. [Correction of the activity of certain enzymes in the rat liver mitochondrial electron transport chain by derivatives of alpha-tocopheryl acetate in toxic damage to the liver].
Kovalenko VN; Blazhchuk IS; Shaiakhmetova AM; Kuz'menko IV
Ukr Biokhim Zh (1999); 1999; 71(4):30-4. PubMed ID: 10791053
[TBL] [Abstract][Full Text] [Related]
18. Succinate-cytochrome c reductase: assessment of its value in the investigation of defects of the respiratory chain.
Taylor RW; Birch-Machin MA; Bartlett K; Turnbull DM
Biochim Biophys Acta; 1993 Jun; 1181(3):261-5. PubMed ID: 8391327
[TBL] [Abstract][Full Text] [Related]
19. Defects of the respiratory chain in the normal human liver and in cirrhosis during aging.
Müller-Höcker J; Aust D; Rohrbach H; Napiwotzky J; Reith A; Link TA; Seibel P; Hölzel D; Kadenbach B
Hepatology; 1997 Sep; 26(3):709-19. PubMed ID: 9303502
[TBL] [Abstract][Full Text] [Related]
20. Mitochondrial respiratory chain activity in the human brain as a function of age.
Ojaimi J; Masters CL; Opeskin K; McKelvie P; Byrne E
Mech Ageing Dev; 1999 Nov; 111(1):39-47. PubMed ID: 10576606
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]