These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

157 related articles for article (PubMed ID: 3132077)

  • 1. Deficiency of subunits of Complex I and mitochondrial encephalomyopathy.
    Ichiki T; Tanaka M; Nishikimi M; Suzuki H; Ozawa T; Kobayashi M; Wada Y
    Ann Neurol; 1988 Mar; 23(3):287-94. PubMed ID: 3132077
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Findings in muscle in complex I (NADH coenzyme Q reductase) deficiency.
    Koga Y; Nonaka I; Kobayashi M; Tojyo M; Nihei K
    Ann Neurol; 1988 Dec; 24(6):749-56. PubMed ID: 3144939
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Two cases of NADH-coenzyme Q reductase deficiency: relationship to MELAS syndrome.
    Kobayashi M; Morishita H; Sugiyama N; Yokochi K; Nakano M; Wada Y; Hotta Y; Terauchi A; Nonaka I
    J Pediatr; 1987 Feb; 110(2):223-7. PubMed ID: 3100753
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Disproportionate deficiency of iron-sulfur clusters and subunits of complex I in mitochondrial encephalomyopathy.
    Ichiki T; Tanaka M; Kobayashi M; Sugiyama N; Suzuki H; Nishikimi M; Ohnishi T; Nonaka I; Wada Y; Ozawa T
    Pediatr Res; 1989 Feb; 25(2):194-201. PubMed ID: 2493147
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Variation in the levels of complex I subunits among tissues in a patient with mitochondrial encephalomyopathy and renal dysfunction.
    Tanaka M; Nishikimi M; Suzuki H; Ozawa T; Ichiki T; Kobayashi M; Wada Y
    Biochem Int; 1987 Apr; 14(4):735-9. PubMed ID: 3134026
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Mitochondrial myopathy and encephalopathy: three cases--a deficiency of NADH-CoQ dehydrogenase?
    Holliday PL; Climie AR; Gilroy J; Mahmud MZ
    Neurology; 1983 Dec; 33(12):1619-22. PubMed ID: 6417559
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. A mitochondrial encephalomyopathy with cardiomyopathy. A case revealing a defect of complex I in the respiratory chain.
    Nishizawa M; Tanaka K; Shinozawa K; Kuwabara T; Atsumi T; Miyatake T; Ohama E
    J Neurol Sci; 1987 Apr; 78(2):189-201. PubMed ID: 3106581
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes syndrome and NADH-CoQ reductase deficiency.
    Kobayashi M; Morishita H; Sugiyama N; Yokochi K; Nakano M; Wada Y; Hotta Y; Terauchi A; Nonaka I
    J Inherit Metab Dis; 1986; 9(3):301-4. PubMed ID: 3099078
    [No Abstract]   [Full Text] [Related]  

  • 11. Vascular involvement in mitochondrial myopathy.
    Sakuta R; Nonaka I
    Ann Neurol; 1989 Jun; 25(6):594-601. PubMed ID: 2500889
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Delayed manifestation of mitochondrial myopathy--complex I and IV deficiency of the mitochondrial respiratory chain with progressive paresis].
    Beyenburg S; von Wersebe O; Zierz S
    Nervenarzt; 1991 Aug; 62(8):506-11. PubMed ID: 1658669
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [Complex I (NADH coenzyme-Q-reductase) deficiency, MELAS syndrome and hypertrophic cardiomyopathy].
    Márquez C; Bautista J; Arenas J; Segura D; Chinchón I; Rafel E; Campos Y; Huerta R
    Neurologia; 1991 May; 6(5):185-7. PubMed ID: 1908255
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. [A case of mitochondrial encephalomyopathy with a defect in electron transport at complex I and IV in skeletal muscle showing peripheral neuropathy].
    Ohnishi A; Nakano S; Hashimoto T; Tsuji S; Murai Y
    Rinsho Shinkeigaku; 1988 Jan; 28(1):107-11. PubMed ID: 2838209
    [No Abstract]   [Full Text] [Related]  

  • 16. Partial deficiency of complexes I and IV of the mitochondrial respiratory chain in skeletal muscle of two patients with mitochondrial myopathy.
    Bleistein J; Zierz S
    J Neurol; 1989 May; 236(4):218-22. PubMed ID: 2547913
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. [Kearns-Sayre syndrome: mitochondrial encephalomyopathy caused by deficiency of the respiratory chain].
    Desnuelle C; Pellissier JF; Serratrice G; Pouget J; Turnbull DM
    Rev Neurol (Paris); 1989; 145(12):842-50. PubMed ID: 2559448
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Deficiency of subunits in heart mitochondrial NADH-ubiquinone oxidoreductase of a patient with mitochondrial encephalomyopathy and cardiomyopathy.
    Tanaka M; Nishikimi M; Suzuki H; Ozawa T; Nishizawa M; Tanaka K; Miyatake T
    Biochem Biophys Res Commun; 1986 Oct; 140(1):88-93. PubMed ID: 3022724
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 8.