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Journal Abstract Search

168 related items for PubMed ID: 7186478

  • 1. Hereditary disorders of erythrocyte enzymes in non-glycolytic metabolic pathways.
    Paglia DE, Valentine WN.
    Haematologia (Budap); 1982 Dec; 15(4):381-8. PubMed ID: 7186478
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  • 2. [Hemolytic anemia due to abnormalities in erythrocyte nucleotide metabolism].
    Masuda M, Mizoguchi H.
    Nihon Rinsho; 1996 Sep; 54(9):2473-7. PubMed ID: 8890581
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  • 3. Hereditary hemolytic anemia with human erythrocyte pyrimidine 5'-nucleotidase deficiency.
    Valentine WN, Fink K, Paglia DE, Harris SR, Adams WS.
    J Clin Invest; 1974 Oct; 54(4):866-79. PubMed ID: 4372252
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  • 4. Disorders associated with purine and pyrimidine metabolism.
    Edwards NL, Fox IH.
    Spec Top Endocrinol Metab; 1984 Oct; 6():95-140. PubMed ID: 6098039
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  • 7. Decreased S-adenosylhomocysteine hydrolase in inborn errors of purine metabolism.
    Kaminska JE, Fox IH.
    J Lab Clin Med; 1980 Jul; 96(1):141-7. PubMed ID: 7391654
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  • 11. Red cell enzyme deficiencies as non-disease.
    Beutler E.
    Biomed Biochim Acta; 1983 Jul; 42(11-12):S234-41. PubMed ID: 6232925
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  • 12. Molecular basis of erythroenzymopathies associated with hereditary hemolytic anemia: tabulation of mutant enzymes.
    Miwa S, Fujii H.
    Am J Hematol; 1996 Feb; 51(2):122-32. PubMed ID: 8579052
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  • 15. Red cell nucleotide abnormalities.
    Paglia DE, Valentine WN.
    Prog Clin Biol Res; 1984 Feb; 165():213-25. PubMed ID: 6095314
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  • 17. Immunodeficiency syndromes associated with inherited metabolic disorders.
    Cowan MJ, Ammann AJ.
    Clin Haematol; 1981 Feb; 10(1):139-59. PubMed ID: 6260406
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  • 19. [A new erythroenzymopathy: congenital non-spherocytic hemolytic anemia and hereditary erythrocytic adenylate kinase deficiency].
    Boivin P, Galand C, Hakim J, Simony D, Seligman M.
    Presse Med (1893); 1971 Jan 30; 79(6):215-8. PubMed ID: 5546784
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  • 20. Disorders of purine and pyrimidine metabolism.
    Nyhan WL.
    Mol Genet Metab; 2005 Jan 30; 86(1-2):25-33. PubMed ID: 16176880
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