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 *

131 related articles for article (PubMed ID: 7229653)

  • 1. Mitochondrial myopathy. Biochemical studies revealing a deficiency of NADH--cytochrome b reductase activity.
    Land JM; Morgan-Hughes JA; Clark JB
    J Neurol Sci; 1981 Apr; 50(1):1-13. PubMed ID: 7229653
    [TBL] [Abstract][Full Text] [Related]  

  • 2. A mitochondrial myopathy with a deficiency of respiratory chain NADH-CoQ reductase activity.
    Morgan-Hughes JA; Darveniza P; Landon DN; Land JM; Clark JB
    J Neurol Sci; 1979 Sep; 43(1):27-46. PubMed ID: 521828
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Tissue specific defect of complex I of the mitochondrial respiratory chain.
    Watmough NJ; Birch-Machin MA; Bindoff LA; Aynsley-Green A; Simpson K; Ragan CI; Sherratt HS; Turnbull DM
    Biochem Biophys Res Commun; 1989 Apr; 160(2):623-7. PubMed ID: 2719685
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. [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]  

  • 6. 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]  

  • 7. Childhood mitochondrial myopathy with ophthalmoplegia.
    Land JM; Hockaday JM; Hughes JT; Ross BD
    J Neurol Sci; 1981 Sep; 51(3):371-82. PubMed ID: 7276984
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mitochondrial encephalomyopathy. Association with an NADH dehydrogenase deficiency.
    van Erven PM; Gabreëls FJ; Ruitenbeek W; Renier WO; Fischer JC
    Arch Neurol; 1987 Jul; 44(7):775-8. PubMed ID: 3593065
    [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. 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]  

  • 11. Succinic acidemia: a new syndrome of organic acidemia associated with congenital lactic acidosis and decreased NADH-cytochrome c reductase activity.
    Asano K; Miyamoto I; Matsushita T; Murakami Y; Minoura S; Wagatsuma T; Oshima M
    Clin Chim Acta; 1988 Apr; 173(3):305-12. PubMed ID: 3383430
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Mitochondrial NADH dehydrogenase in iron-deficient and iron-repleted rat muscle: an EPR and work performance study.
    Ohira Y; Hegenauer J; Strause L; Chen CS; Saltman P; Beinert H
    Br J Haematol; 1982 Dec; 52(4):623-30. PubMed ID: 6291576
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Mitochondrial myopathy with partial cytochrome oxidase deficiency and impaired oxidation of NADH-linked substrates.
    Sherratt HS; Cartlidge NE; Johnson MA; Turnbull DM
    J Inherit Metab Dis; 1984; 7 Suppl 2():107-8. PubMed ID: 6090805
    [No Abstract]   [Full Text] [Related]  

  • 14. 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]  

  • 15. 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]  

  • 16. Mitochondrial encephalo-neuro-myopathy with myoclonus epilepsy, basal nuclei calcification and hyperlactacidemia.
    Federico A; Cornelio F; Di Donato S; Ederli E; Fabrizi GM; Manneschi L; Guazzi GC
    Ital J Neurol Sci; 1988 Feb; 9(1):65-71. PubMed ID: 3356526
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [A case of mitochondrial encephalomyopathy with cardiomyopathy due to decreased complex I and IV activities].
    Kajiyama M; Kawamura I; Fujita A; Hamamoto K; Nishi Y; Kitano A; Matsuda I; Ohtani Y; Miike T
    No To Hattatsu; 1989 Jul; 21(4):369-73. PubMed ID: 2551357
    [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. 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]  

  • 20. 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]  

    [Next]    [New Search]
    of 7.