BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

148 related articles for article (PubMed ID: 2172646)

  • 1. Heterogeneous tissue expression of enzyme defects in mitochondrial myopathies.
    Sperl W; Ruitenbeek W; Trijbels JM; Korenke GC; Sengers RC
    J Inherit Metab Dis; 1990; 13(3):359-62. PubMed ID: 2172646
    [No Abstract]   [Full Text] [Related]  

  • 2. [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]  

  • 3. 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]  

  • 4. Deficiency of the iron-sulfur clusters of mitochondrial reduced nicotinamide-adenine dinucleotide-ubiquinone oxidoreductase (complex I) in an infant with congenital lactic acidosis.
    Moreadith RW; Batshaw ML; Ohnishi T; Kerr D; Knox B; Jackson D; Hruban R; Olson J; Reynafarje B; Lehninger AL
    J Clin Invest; 1984 Sep; 74(3):685-97. PubMed ID: 6432847
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. 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]  

  • 7. Partial deficiency of subunits in complex I or IV of patients with mitochondrial myopathies.
    Tanaka M; Nishikimi M; Suzuki H; Ozawa T; Koga Y; Nonaka I
    Biochem Int; 1987 Mar; 14(3):525-30. PubMed ID: 2884999
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Variability in the activity of respiratory chain enzymes in mitochondrial myopathies.
    Koga Y; Nonaka I; Sunohara N; Yamanaka R; Kumagai K
    Acta Neuropathol; 1988; 76(2):135-41. PubMed ID: 2841822
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [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]  

  • 11. 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]  

  • 12. [Muscle pathology in mitochondrial myopathy].
    Nonaka I
    No To Hattatsu; 1987 Mar; 19(2):110-7. PubMed ID: 3030377
    [No Abstract]   [Full Text] [Related]  

  • 13. 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]  

  • 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. 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]  

  • 16. 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]  

  • 17. [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]  

  • 18. Estimation of NADH oxidation in human skeletal muscle mitochondria.
    Fischer JC; Ruitenbeek W; Trijbels JM; Veerkamp JH; Stadhouders AM; Sengers RC; Janssen AJ
    Clin Chim Acta; 1986 Mar; 155(3):263-73. PubMed ID: 3011316
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Myalgia with partial defects of mitochondrial enzyme and myoadenylate deaminase.
    Tsao CY; McComb RD
    Pediatr Neurol; 1990; 6(1):65. PubMed ID: 2155618
    [No Abstract]   [Full Text] [Related]  

  • 20. Mitochondrial encephalomyopathy with decreased succinate-cytochrome c reductase activity.
    Riggs JE; Schochet SS; Fakadej AV; Papadimitriou A; DiMauro S; Crosby TW; Gutmann L; Moxley RT
    Neurology; 1984 Jan; 34(1):48-53. PubMed ID: 6318158
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.