124 related articles for article (PubMed ID: 9255214)
1. 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]
2. [Pure mitochondrial myopathy].
Murakami N; Sakuta R
Ryoikibetsu Shokogun Shirizu; 2001; (36):186-9. PubMed ID: 11596366
[No Abstract] [Full Text] [Related]
3. 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]
4. [Abnormality in the mitochondrial energy-producing system].
Ozawa T; Tanaka M
Tanpakushitsu Kakusan Koso; 1988 Apr; 33(5):824-7. PubMed ID: 2855955
[No Abstract] [Full Text] [Related]
5. Favourable clinical course in an infant with severe deficiency of complex III of the respiratory chain combined with less severe deficiencies of complexes I, II and IV.
Rubio-Gozalbo ME; Ruitenbeek W; Bentlage HA; Schägger H; Sengers RC; Trijbels JM; ter Laak HJ; Mariman EC; Bakker MM; de Jager J; Smeitink JA
Eur J Pediatr; 1997 Dec; 156(12):931-4. PubMed ID: 9453375
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. [Complex II (succinate-ubiquinone reductase) deficiency].
Nonaka I
Ryoikibetsu Shokogun Shirizu; 2001; (36):132-4. PubMed ID: 11596343
[No Abstract] [Full Text] [Related]
8. Combined 3-methylglutaconic and 3-hydroxy-3-methylglutaric aciduria with endocardial fibroelastosis and dilatative cardiomyopathy in male and female siblings with partial deficiency of complex II/III in fibroblasts.
Ruesch S; Krähenbühl S; Kleinle S; Liechti-Gallati S; Schaffner T; Wermuth B; Weber J; Wiesmann UN
Enzyme Protein; 1996; 49(5-6):321-9. PubMed ID: 9252790
[TBL] [Abstract][Full Text] [Related]
9. The use of chorionic villi in prenatal diagnosis of mitochondriopathies.
Ruitenbeek W; Sengers RC; Trijbels JM; Janssen AJ; Bakkeren JA
J Inherit Metab Dis; 1992; 15(3):303-6. PubMed ID: 1328761
[No Abstract] [Full Text] [Related]
10. 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]
11. Multiple defects of the mitochondrial respiratory chain in a mitochondrial encephalopathy (MERRF): a clinical, biochemical and molecular study.
Bindoff LA; Desnuelle C; Birch-Machin MA; Pellissier JF; Serratrice G; Dravet C; Bureau M; Howell N; Turnbull DM
J Neurol Sci; 1991 Mar; 102(1):17-24. PubMed ID: 1649912
[TBL] [Abstract][Full Text] [Related]
12. Biochemical and molecular aspects of human mitochondrial respiratory chain disorders.
Cooper JM; Schapira AH; Holt IJ; Toscano A; Harding AE; Morgan-Hughes JA; Clark JB
Biochem Soc Trans; 1990 Aug; 18(4):517-9. PubMed ID: 2177405
[No Abstract] [Full Text] [Related]
13. 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]
14. 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]
15. Mitochondrial myopathies.
DiMauro S; Bonilla E; Zeviani M; Servidei S; DeVivo DC; Schon EA
J Inherit Metab Dis; 1987; 10 Suppl 1():113-28. PubMed ID: 2824920
[TBL] [Abstract][Full Text] [Related]
16. Multiple defects of the respiratory chain including complex II in a family with myopathy and encephalopathy.
Desnuelle C; Birch-Machin M; Pellissier JF; Bindoff LA; Ackrell BA; Turnbull DM
Biochem Biophys Res Commun; 1989 Sep; 163(2):695-700. PubMed ID: 2551272
[TBL] [Abstract][Full Text] [Related]
17. [Electron transfer complex II deficiency].
Goto Y
Ryoikibetsu Shokogun Shirizu; 1998; (19 Pt 2):491-3. PubMed ID: 9645117
[No Abstract] [Full Text] [Related]
18. Depletion of mitochondrial DNA in the liver of an infant with neonatal giant cell hepatitis.
Müller-Höcker J; Muntau A; Schäfer S; Jaksch M; Staudt F; Pongratz D; Taanman JW
Hum Pathol; 2002 Feb; 33(2):247-53. PubMed ID: 11957153
[TBL] [Abstract][Full Text] [Related]
19. Mitochondrial disorders of the nervous system: clinical, biochemical, and molecular genetic features.
Thyagarajan D; Byrne E
Int Rev Neurobiol; 2002; 53():93-144. PubMed ID: 12512338
[No Abstract] [Full Text] [Related]
20. A high rate (20%-30%) of parental consanguinity in cytochrome-oxidase deficiency.
von Kleist-Retzow JC; Cormier-Daire V; de Lonlay P; Parfait B; Chretien D; Rustin P; Feingold J; Rötig A; Munnich A
Am J Hum Genet; 1998 Aug; 63(2):428-35. PubMed ID: 9683589
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
