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PUBMED FOR HANDHELDS

Journal Abstract Search


219 related items for PubMed ID: 5969464

  • 21. [Hereditary glucose-6-phosphate dehydrogenase deficiency in human erythrocytes].
    Hurwic M.
    Postepy Hig Med Dosw; 1970; 24(4):497-522. PubMed ID: 5458083
    [No Abstract] [Full Text] [Related]

  • 22. Glucose-6-phosphate dehydrogenase and other genetic factors interacting with drugs.
    Luzzatto L.
    Prog Clin Biol Res; 1986; 214():385-99. PubMed ID: 3725767
    [No Abstract] [Full Text] [Related]

  • 23. [Lead poisoning in a woman with favic erythrocytes].
    Saita G, Lussana S.
    Med Lav; 1971 Jan; 62(1):22-7. PubMed ID: 5095327
    [No Abstract] [Full Text] [Related]

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  • 25. [Favism, hemoglobin H, alpha-thalassemia and hemoglobinopathy in various Sardinian families. Studies on glucose-6-phosphate dehydrogenase].
    Pabis A, Alessio L, Fiorelli G, Sulis E, Dioguardi N.
    Folia Haematol Int Mag Klin Morphol Blutforsch; 1969 Jan; 91(1):56-60. PubMed ID: 4180962
    [No Abstract] [Full Text] [Related]

  • 26. Leucocyte glucose-6-phosphate dehydrogenase (G-6-PD) activity in G-6-PD deficient Chinese.
    Chen SH, Lin KS, Chen CL.
    Proc Natl Sci Counc Repub China B; 1985 Oct; 9(4):251-4. PubMed ID: 4095209
    [Abstract] [Full Text] [Related]

  • 27. Glucose-6-phosphate dehydrogenase of leukocyte subpopulations in normal and enzyme deficient individuals.
    Morellini M, Colonna-Romano S, Meloni T, Battistuzzi G, Gandini E.
    Haematologica; 1985 Oct; 70(5):390-5. PubMed ID: 3937773
    [No Abstract] [Full Text] [Related]

  • 28. [Genetic questionnaire. Genetic counseling for a patient with the complex association of G-6-PD deficiency, Gronblad-Strandberg syndrome (pseudo-xanthoma elasticum) and epilepsy].
    Klein D, Gauthier G, Babel J.
    J Genet Hum; 1973 Mar; 21(1):57-62. PubMed ID: 4742124
    [No Abstract] [Full Text] [Related]

  • 29. [Detection of G-6-PD deficiency in children born at the Giannina Gaslini Institute, using a rapid screening method].
    Chierici M, Cingolani M, Massone L, Milone S.
    Quad Sclavo Diagn; 1980 Mar; 16(1):119-28. PubMed ID: 7244085
    [No Abstract] [Full Text] [Related]

  • 30. [Association of a triple genetic erythrocyte defect: thalassemia, sickle cell disease and glucose-6-phosphate dehydrogenase deficiency in a child of Calabro-Sardinian origin].
    Sansone G, Vallarino G, Centa A.
    Haematologica; 1967 Mar; 52(6):479-92. PubMed ID: 4976069
    [No Abstract] [Full Text] [Related]

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  • 32. [Preliminary observations on the incidence of neoplasms and on the enzymatic and proliferative behavior of the tumor tissue in individuals deficient in glucose-6-phosphate dehydrogenase (G6-PD)].
    Sulis E, Spano G.
    Boll Soc Ital Biol Sper; 1968 Aug 15; 44(15):1246-9. PubMed ID: 5703256
    [No Abstract] [Full Text] [Related]

  • 33. [Behavior of glucose-6-phosphate dehydrogenase (G-6-PD) in the granulocytes and myelocytes of leukemic patients with and without the favic defect].
    Idéo G, Sulis E, Spano G, Podda M, Dioguardi N.
    Boll Soc Ital Biol Sper; 1967 Feb 15; 43(3):136-9. PubMed ID: 6048354
    [No Abstract] [Full Text] [Related]

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  • 35. [Favism. Glucose-6-phosphate dehydrogenase deficiency].
    Matzkies F.
    Fortschr Med; 1973 Oct 15; 28(11):1097-9. PubMed ID: 4755370
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  • 40. [Hereditary and epidemiological aspects of erythrocyte glucose-6-phosphate dehydrogenase deficiency in Mexico].
    Lisker R, Pérez Briceño R, Sosa R, Shein M.
    Gac Med Mex; 1976 Jun 15; 111(6):454-8. PubMed ID: 964538
    [No Abstract] [Full Text] [Related]


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