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Journal Abstract Search

241 related items for PubMed ID: 10474511

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  • 6. Advances in hereditary red cell enzyme anomalies.
    Kahn A, Kaplan JC, Dreyfus JC.
    Hum Genet; 1979; 50(1):1-27. PubMed ID: 157322
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  • 9. [New advances in the diagnosis of erythro-enzymopathies].
    Vives Corrons JL.
    Sangre (Barc); 1982; 27(5):923-43. PubMed ID: 6301081
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  • 10. Molecular aspects of erythroenzymopathies associated with hereditary hemolytic anemia.
    Miwa S, Fujii H.
    Am J Hematol; 1985 Jul; 19(3):293-305. PubMed ID: 2990202
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  • 14. Erythrocyte pyruvate kinase- and glucose phosphate isomerase deficiency: perturbation of glycolysis by structural defects and functional alterations of defective enzymes and its relation to the clinical severity of chronic hemolytic anemia.
    Lakomek M, Winkler H.
    Biophys Chem; 1997 Jun 30; 66(2-3):269-84. PubMed ID: 9362562
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  • 15. [Red cell enzyme deficiencies - clinical manifestation and pathophysiology (author's transl)].
    Gahr M.
    Monatsschr Kinderheilkd; 1981 Aug 30; 129(8):444-53. PubMed ID: 6116183
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  • 16. Hereditary disorders of enzymes in the Embden-Meyerhof pathway of glycolysis.
    Miwa S.
    Haematologia (Budap); 1982 Dec 30; 15(4):371-9. PubMed ID: 6225712
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  • 18. Clinical consequences of enzyme deficiencies in the erythrocyte.
    Netzloff ML.
    Ann Clin Lab Sci; 1980 Dec 30; 10(5):414-24. PubMed ID: 6252820
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