138 related articles for article (PubMed ID: 2176453)
1. Defects of the respiratory chain.
Bindoff LA; Turnbull DM
Baillieres Clin Endocrinol Metab; 1990 Sep; 4(3):583-619. PubMed ID: 2176453
[No Abstract] [Full Text] [Related]
2. Mitochondrial myopathies involving the respiratory chain: a biochemical analysis.
Takamiya S; Yanamura W; Capaldi RA; Kennaway NG; Bart R; Sengers RC; Trijbels JM; Ruitenbeek W
Ann N Y Acad Sci; 1986; 488():33-43. PubMed ID: 3034117
[No Abstract] [Full Text] [Related]
3. Mitochondrial myopathies. Clinical, morphological and biochemical aspects.
Sengers RC; Stadhouders AM; Trijbels JM
Eur J Pediatr; 1984 Feb; 141(4):192-207. PubMed ID: 6329761
[No Abstract] [Full Text] [Related]
4. Molecular basis of mitochondrial myopathies.
Lancet; 1988 Apr; 1(8590):884-5. PubMed ID: 2895390
[No Abstract] [Full Text] [Related]
5. The mitochondrial myopathies. Defects of the mitochondrial respiratory chain and oxidative phosphorylation system.
Morgan-Hughes JA; Cooper JM; Schapira AH; Hayes DJ; Clark JB
Electroencephalogr Clin Neurophysiol Suppl; 1987; 39():103-14. PubMed ID: 2888641
[No Abstract] [Full Text] [Related]
6. 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]
7. 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]
8. 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]
9. [Clinical and biochemical approach to mitochondrial cytopathy--defects of the respiratory chain].
Kobayashi M
No To Hattatsu; 1987 Mar; 19(2):132-9. PubMed ID: 3030379
[No Abstract] [Full Text] [Related]
10. 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]
11. [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]
12. Impaired mitochondrial beta-oxidation in a patient with an abnormality of the respiratory chain. Studies in skeletal muscle mitochondria.
Watmough NJ; Bindoff LA; Birch-Machin MA; Jackson S; Bartlett K; Ragan CI; Poulton J; Gardiner RM; Sherratt HS; Turnbull DM
J Clin Invest; 1990 Jan; 85(1):177-84. PubMed ID: 2153151
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
15. 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]
16. [A case of late-onset and slowly progressive mitochondrial myopathy with abnormalities of complexes in electron-transfer system].
Shibuya S; Wakayama Y; Okayasu H; Tanaka M; Ozawa T
Rinsho Shinkeigaku; 1988 Oct; 28(10):1147-51. PubMed ID: 2851402
[No Abstract] [Full Text] [Related]
17. [Mitochondrial encephalomyopathy].
Ozawa T; Tanaka M
Tanpakushitsu Kakusan Koso; 1990 May; 35(7 Suppl):1236-45. PubMed ID: 2162552
[No Abstract] [Full Text] [Related]
18. Defects in oxidative phosphorylation. Biochemical investigations in skeletal muscle and expression of the lesion in other cells.
Scholte HR; Busch HF; Luyt-Houwen IE; Vaandrager-Verduin MH; Przyrembel H; Arts WF
J Inherit Metab Dis; 1987; 10 Suppl 1():81-97. PubMed ID: 2824921
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Molecular basis of mitochondrial myopathies: polypeptide analysis in complex-I deficiency.
Schapira AH; Cooper JM; Morgan-Hughes JA; Patel SD; Cleeter MJ; Ragan CI; Clark JB
Lancet; 1988 Mar; 1(8584):500-3. PubMed ID: 2893919
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
