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 *

92 related articles for article (PubMed ID: 982428)

  • 1. Citrate treatment in a patient with pyruvate decarboxylase deficiency.
    Oka Y; Matsuda I; Arashima S; Anakura M; Mitsuyama T
    Tohoku J Exp Med; 1976 Feb; 118(2):131-5. PubMed ID: 982428
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Pyruvate decarboxylase deficiency in a patient with Leigh's encephalomyelopathy.
    Ohtake M; Takada G; Miyabayashi S; Arai N; Tada K; Morinaga S
    Tohoku J Exp Med; 1982 Aug; 137(4):379-86. PubMed ID: 7123539
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The effect of a high fat diet on pyruvate decarboxylase deficiency without central nervous system involvement.
    Kodama S; Yagi R; Ninomiya M; Goji K; Takahashi T; Morishita Y; Matsuo T
    Brain Dev; 1983; 5(4):381-9. PubMed ID: 6416099
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A case of pyruvate carboxylase deficiency with later prenatal diagnosis of an unaffected sibling.
    Tsuchiyama A; Oyanagi K; Hirano S; Tachi N; Sogawa H; Wagatsuma K; Nakao T; Tsugawa S; Kawamura Y
    J Inherit Metab Dis; 1983; 6(3):85-8. PubMed ID: 6422150
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Episodic weakness in pyruvate decarboxylase deficiency.
    Evans OB
    J Pediatr; 1984 Dec; 105(6):961-3. PubMed ID: 6502351
    [No Abstract]   [Full Text] [Related]  

  • 6. Pyruvate decarboxylase deficiency in subacute necrotizing encephalomyelopathy.
    Evans OB
    Arch Neurol; 1981 Aug; 38(8):515-9. PubMed ID: 7247788
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Enzymologic studies and therapy of Leigh's disease associated with pyruvate decarboxylase deficiency.
    Toshima K; Kuroda Y; Hashimoto T; Ito M; Watanabe T; Miyao M; Ii K
    Pediatr Res; 1982 Jun; 16(6):430-5. PubMed ID: 7099758
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Leigh's disease with decreased activities of pyruvate carboxylase and pyruvate decarboxylase.
    Van Biervliet JP; Duran M; Wadman SK; Koster JF; van Rossum A
    J Inherit Metab Dis; 1980; 2(1):15-8. PubMed ID: 6796755
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Congenital lactic acidosis associated with pyruvate carboxylase deficiency. Repository identification No. GM6056.
    Oizumi J; Donnell GN; Ng WG; Mulivor RA; Greene AE; Coriell LL
    Cytogenet Cell Genet; 1984; 38(1):80. PubMed ID: 6705569
    [No Abstract]   [Full Text] [Related]  

  • 10. Thiamin deficiency effects on rat leukocyte pyruvate decarboxylation rates.
    Hathcock JN
    Am J Clin Nutr; 1978 Feb; 31(2):250-2. PubMed ID: 623048
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Lipid storage myopathies--carnitine deficiency, carnitine palmitoyltransferase deficiency, pyruvate decarboxylase deficiency].
    Itagaki Y; Nishitani H
    Nihon Rinsho; 1990 Jul; 48(7):1510-6. PubMed ID: 2402068
    [No Abstract]   [Full Text] [Related]  

  • 12. Urinary organic acids in a case of congenital lactic acidosis due to pyruvate decarboxylase deficiency.
    Chalmers RA; Lawson AM; Borud O
    J Inherit Metab Dis; 1978; 1(1):15-6. PubMed ID: 117229
    [No Abstract]   [Full Text] [Related]  

  • 13. Gas chromatographic and mass spectrometric studies on urinary organic acids in a patient with congenital lactic acidosis due to pyruvate decarboxylase deficiency.
    Chalmers RA; Lawson AM; Borud O
    Clin Chim Acta; 1977 Jun; 77(2):117-24. PubMed ID: 19171
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Partial pyruvate decarboxylase deficiency with profound lactic acidosis and hyperammonemia: responses to dichloroacetate and benzoate.
    McCormick K; Viscardi RM; Robinson B; Heininger J
    Am J Med Genet; 1985 Oct; 22(2):291-9. PubMed ID: 4050860
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A defect in pyruvate decarboxylase in a child with an intermittent movement disorder.
    Blass JP; Avigan J; Uhlendorf BW
    J Clin Invest; 1970 Mar; 49(3):423-32. PubMed ID: 4313434
    [TBL] [Abstract][Full Text] [Related]  

  • 16. The disappearance of pyruvic decarboxylase and alpha-ketoglutaric decarboxylase from pigeon muscles on thiamine deficient diets.
    MONFOORT CH
    Arch Int Physiol Biochim; 1954 Dec; 62(4):571-2. PubMed ID: 13218838
    [No Abstract]   [Full Text] [Related]  

  • 17. The disappearance of pyruvic decarboxylase and alpha-ketoglutaric decarboxylase from pigeon muscles on thiamine-deficient diets.
    MONFOORT CH
    Biochim Biophys Acta; 1955 Feb; 16(2):219-28. PubMed ID: 14363255
    [No Abstract]   [Full Text] [Related]  

  • 18. Pyruvate decarboxylase activity in familial intermittent cerebellar ataxia.
    Farmer TW; Veath L; Miller AL; O'Brien JS
    Trans Am Neurol Assoc; 1973; 98():260-2. PubMed ID: 4784948
    [No Abstract]   [Full Text] [Related]  

  • 19. Absence of pyruvate decarboxylase activity in man: a cause of congenital lactic acidosis.
    Farrell DF; Clark AF; Scott CR; Wennberg RP
    Science; 1975 Mar; 187(4181):1082-4. PubMed ID: 803713
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Pyruvate decarboxylase III. Specificity restrictions for thiamine pyrophosphate in the protein association step, sub-unit structure.
    Gounaris AD; Turkenkopf I; Civerchia LL; Greenlie J
    Biochim Biophys Acta; 1975 Oct; 405(2):492-9. PubMed ID: 1101964
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 5.