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Journal Abstract Search

197 related items for PubMed ID: 6225712

  • 1. Hereditary disorders of enzymes in the Embden-Meyerhof pathway of glycolysis.
    Miwa S.
    Haematologia (Budap); 1982 Dec; 15(4):371-9. PubMed ID: 6225712
    [Abstract] [Full Text] [Related]

  • 2. Hereditary disorders of red cell enzymes in the Embden-Meyerhof pathway.
    Miwa S.
    Am J Hematol; 1983 Jun; 14(4):381-91. PubMed ID: 6222645
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  • 5. Pyruvate kinase deficiency and other enzymopathies of the Embden--Meyerhof pathway.
    Miwa S.
    Clin Haematol; 1981 Feb; 10(1):57-80. PubMed ID: 6260408
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  • 8. [Erythrocyte enzyme defects and their clinical significance (author's transl)].
    Schröter W.
    Monatsschr Kinderheilkd; 1981 Aug; 129(8):432-43. PubMed ID: 6116182
    [No Abstract] [Full Text] [Related]

  • 9. Advances in hereditary red cell enzyme anomalies.
    Kahn A, Kaplan JC, Dreyfus JC.
    Hum Genet; 1979 Aug; 50(1):1-27. PubMed ID: 157322
    [No Abstract] [Full Text] [Related]

  • 10. [Enzyme deficiencies in glycolysis and nucleotide metabolism of red blood cells in nonspherocytic hemolytic anemia (author's transl)].
    Waller HD, Benöhr HC.
    Klin Wochenschr; 1976 Sep 01; 54(17):803-21. PubMed ID: 184346
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  • 11. Clinical consequences of enzyme deficiencies in the erythrocyte.
    Netzloff ML.
    Ann Clin Lab Sci; 1980 Sep 01; 10(5):414-24. PubMed ID: 6252820
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  • 12. [Defects in erythrocyte glycolysis enzymes as the cause of nonspherocytic hemolytic anemia].
    Ulrich Trenckmann.
    Z Gesamte Inn Med; 1976 May 01; 31(9):257-61. PubMed ID: 134517
    [Abstract] [Full Text] [Related]

  • 13. [Hereditary hemolytic anemia due to erythrocyte enzyme deficiency (author's transl)].
    Miwa S.
    Nihon Naika Gakkai Zasshi; 1976 Feb 01; 65(2):111-27. PubMed ID: 135034
    [No Abstract] [Full Text] [Related]

  • 14. Molecular aspects of erythroenzymopathies associated with hereditary hemolytic anemia.
    Miwa S, Fujii H.
    Am J Hematol; 1985 Jul 01; 19(3):293-305. PubMed ID: 2990202
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  • 15. Hemolytic anemias and erythrocyte enzymopathies.
    Valentine WN, Tanaka KR, Paglia DE.
    Ann Intern Med; 1985 Aug 01; 103(2):245-57. PubMed ID: 2990276
    [Abstract] [Full Text] [Related]

  • 16. Molecular basis of red cell enzymopathies associated with hereditary nonspherocytic hemolytic anemia.
    Miwa S.
    Haematologia (Budap); 1989 Aug 01; 22(4):215-31. PubMed ID: 2560452
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  • 17. Congenital non-spherocytic haemolytic anaemias.
    Zanella A, Colombo MB, Rossi F, Merati G, Sirchia G.
    Haematologica; 1989 Aug 01; 74(4):387-96. PubMed ID: 2551797
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  • 18. Hemolytic anemias due to erythrocyte enzyme deficiencies.
    Jacobasch G, Rapoport SM.
    Mol Aspects Med; 1996 Apr 01; 17(2):143-70. PubMed ID: 8813716
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  • 19. Deficiencies associated with Embden-Meyerhof pathway and other metabolic pathways.
    Valentine WN.
    Semin Hematol; 1971 Oct 01; 8(4):348-66. PubMed ID: 4256808
    [No Abstract] [Full Text] [Related]

  • 20. A simple screening procedure for glucose phosphate isomerase, phosphofructokinase, aldolase and glyceraldehyde-3-phosphate dehydrogenase deficiencies.
    Vaca G, Medina C, Wunsch C, Garcia-Cruz D, Sanchez-Corona J, Gonzalez-Quiroga G, Cantu JM.
    Ann Genet; 1981 Oct 01; 24(4):251-3. PubMed ID: 6460465
    [Abstract] [Full Text] [Related]

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