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 *

95 related articles for article (PubMed ID: 3103656)

  • 1. [Clinical and biochemical approach to mitochondrial cytopathy--pyruvate dehydrogenase complex deficiency].
    Miyabayashi S; Narisawa K
    No To Hattatsu; 1987 Mar; 19(2):125-31. PubMed ID: 3103656
    [No Abstract]   [Full Text] [Related]  

  • 2. Leigh syndrome associated with a deficiency of the pyruvate dehydrogenase complex: results of treatment with a ketogenic diet.
    Wijburg FA; Barth PG; Bindoff LA; Birch-Machin MA; van der Blij JF; Ruitenbeek W; Turnbull DM; Schutgens RB
    Neuropediatrics; 1992 Jun; 23(3):147-52. PubMed ID: 1641082
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Cytochrome C oxidase-deficient mitochondria in mitochondrial myopathy.
    Haginoya K; Miyabayashi S; Iinuma K; Okino E; Maesaka H; Tada K
    Pediatr Neurol; 1992; 8(1):13-8. PubMed ID: 1313674
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Muscle involvement in pyruvate dehydrogenase complex (PDHC) deficiency.
    Chung SJ; Asoh S; Yamanaka T; Okamura-Oho Y; Toshima K; Woo M; Nonaka I
    Brain Dev; 1987; 9(1):9-15. PubMed ID: 3111288
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mitochondrial encephalomyopathies and cytochrome c oxidase deficiency: muscle culture study.
    Nonaka I; Koga Y; Kikuchi A; Goto Y
    Acta Neuropathol; 1991; 82(4):286-94. PubMed ID: 1662001
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Pyruvate dehydrogenase complex deficiency as a cause of subacute necrotizing encephalopathy (Leigh disease).
    Kretzschmar HA; DeArmond SJ; Koch TK; Patel MS; Newth CJ; Schmidt KA; Packman S
    Pediatrics; 1987 Mar; 79(3):370-3. PubMed ID: 3103091
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Leigh disease with deficiency of lipoamide dehydrogenase: treatment failure with dichloroacetate.
    Craigen WJ
    Pediatr Neurol; 1996 Jan; 14(1):69-71. PubMed ID: 8652022
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Combined deficiencies of the pyruvate dehydrogenase complex and enzymes of the respiratory chain in mitochondrial myopathies.
    Sperl W; Ruitenbeek W; Sengers RC; Trijbels JM; Bentlage H; Wraith JE; Heilmann C; Stöckler S; Binder C; Korenke GC
    Eur J Pediatr; 1992 Mar; 151(3):192-5. PubMed ID: 1601011
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Treatment of congenital lactic acidosis with dichloroacetate.
    Stacpoole PW; Barnes CL; Hurbanis MD; Cannon SL; Kerr DS
    Arch Dis Child; 1997 Dec; 77(6):535-41. PubMed ID: 9496194
    [No Abstract]   [Full Text] [Related]  

  • 11. Leigh syndrome: pyruvate dehydrogenase defect. A case with peripheral neuropathy.
    Chabrol B; Mancini J; Benelli C; Gire C; Munnich A
    J Child Neurol; 1994 Jan; 9(1):52-5. PubMed ID: 8151084
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Proton spectroscopy in patients with Leigh's disease and mitochondrial enzyme deficiency.
    Kruse B; Hanefeld F; Holzbach U; Wilichowski E; Christen HJ; Merboldt KD; Hänicke W; Frahm J
    Dev Med Child Neurol; 1994 Sep; 36(9):839-43. PubMed ID: 7926334
    [No Abstract]   [Full Text] [Related]  

  • 13. Pyruvate dehydrogenase activity is not deficient in the brain of three autopsied cases with Leigh disease (subacute necrotizing encephalomyelopathy, SNE).
    Kustermann-Kuhn B; Harzer K; Schröder R; Permanetter W; Peiffer J
    Hum Genet; 1984; 68(1):51-3. PubMed ID: 6437963
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Abnormalities of pyruvate dehydrogenase complex in brain disease.
    Sheu KF; Szabo P; Ko LW; Hinman LM
    Ann N Y Acad Sci; 1989; 573():378-91. PubMed ID: 2517466
    [No Abstract]   [Full Text] [Related]  

  • 15. Characteristic changes on brain CT in a case of Leigh encephalopathy with deficiency of pyruvate dehydrogenase.
    Arai Y; Miyasato Y; Koide H
    Brain Dev; 1991 Nov; 13(6):457-8. PubMed ID: 1810165
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Pyruvate dehydrogenase deficiency].
    Pedersen S; Bliksrud YT; Selmer KK; Ramm-Pettersen A
    Tidsskr Nor Laegeforen; 2019 Oct; 139(15):. PubMed ID: 31642628
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Outcome of thiamine treatment in a child with Leigh disease due to thiamine-responsive pyruvate dehydrogenase deficiency.
    Di Rocco M; Lamba LD; Minniti G; Caruso U; Naito E
    Eur J Paediatr Neurol; 2000; 4(3):115-7. PubMed ID: 10872106
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [A histological study of mitochondrial myopathy in partial deficiency of pyruvate dehydrogenase complex].
    Suzuki H; Shishikura K; Osawa M; Hirayama Y; Motegi R; Mitsuishi Y; Yamaguchi K; Fukuyama Y
    No To Hattatsu; 1983 Jul; 15(4):290-300. PubMed ID: 6412732
    [No Abstract]   [Full Text] [Related]  

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

    [Next]    [New Search]
    of 5.