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Journal Abstract Search

178 related items for PubMed ID: 4874574

  • 21. Nonspherocytic haemolytic anaemia and severe jaundice in a newborn with partial pyruvate kinase deficiency.
    Volpato S, Vigi V, Cattarozzi G.
    Acta Paediatr Scand; 1968 Jan; 57(1):59-64. PubMed ID: 5637012
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  • 25. [Congenital enzyme defects as a cause of blood disorders].
    Waller HD.
    Wien Klin Wochenschr; 1971 Apr 30; 83(17):293-8. PubMed ID: 5576979
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  • 27. Pyruvate kinase deficiency.
    Tanaka KR, Paglia DE.
    Semin Hematol; 1971 Oct 30; 8(4):367-96. PubMed ID: 4942588
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  • 28. Genetic aspects of enzymopathy.
    Swarup-Mitra S.
    Bull Calcutta Sch Trop Med; 1970 Jul 30; 18(3):88-90. PubMed ID: 5525729
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  • 29. Multiple genotypes, multiple phenotypes, and partial defects.
    Kark RA, Becker DM.
    Muscle Nerve; 1981 Jul 30; 4(1):31-40. PubMed ID: 7015120
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  • 34. [Hereditary hemolytic erythocyte enzymopathies].
    Alekseev GA.
    Klin Med (Mosk); 1980 Sep 30; 58(9):60-8. PubMed ID: 7412196
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  • 36. [Oxygenation curves in enzymopathic hemolytic anemias].
    Rotrekl B, Prokopová M.
    Acta Univ Palacki Olomuc Fac Med; 1984 Sep 30; 106():123-31. PubMed ID: 6242617
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  • 37. [Hematological pathology and clinical enzymology].
    Ballerini G, Castaldi G, Scapoli GL, Meduri P.
    Quad Sclavo Diagn; 1972 Mar 30; 8(1):98-145. PubMed ID: 4268409
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  • 38. Looking for red cell enzyme deficiencies in hemolytic anemias.
    Chapman RG.
    Am J Med Technol; 1971 Nov 30; 37(11):423-7. PubMed ID: 5154328
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  • 39. [Current problems in pharmacogenetics].
    Kudrin AN, Babkina TA, Pashin IuV.
    Ter Arkh; 1976 Nov 30; 48(5):134-40. PubMed ID: 781893
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