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Journal Abstract Search

171 related items for PubMed ID: 4994285

  • 1. [Triple erythrocyte disorders: thalassemia, hemoglobinopathy L Glucose-6-phosphate dehydrogenase deficiency in a girl from Polesine. First study].
    De Filippis A.
    Haematologica; 1969; 54(10):685-702. PubMed ID: 4994285
    [No Abstract] [Full Text] [Related]

  • 2. Haemoglobin O Arab, beta-thalassaemia and glucose-6-phosphate dehydrogenase deficiency in a Hungarian family.
    Horányi M, Szelényi J, Rona G, Lang A, Lehmann H, Hollán SR.
    Folia Haematol Int Mag Klin Morphol Blutforsch; 1980; 107(4):654-60. PubMed ID: 6162733
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  • 3. [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; 52(6):479-92. PubMed ID: 4976069
    [No Abstract] [Full Text] [Related]

  • 4. Clinical and biochemical interactions of glucose-6-phosphate dehydrogenase deficiency and sickle-cell anemia.
    Piomelli S, Reindorf CA, Arzanian MT, Corash LM.
    N Engl J Med; 1972 Aug 03; 287(5):213-7. PubMed ID: 5037496
    [No Abstract] [Full Text] [Related]

  • 5. Hemoglobin A2, E and F levels and the incidence of hemoglobin E, beta-thalassemia, and glucose-6-phosphate dehydrogenase deficiency in lymphoma.
    Panich V, Na-Nakorn S, Piankijagum A.
    J Med Assoc Thai; 1974 Jan 03; 57(1):3-10. PubMed ID: 4814776
    [No Abstract] [Full Text] [Related]

  • 6. [G-6-PD deficiency with hemoglobinopathy and alpha-thalassemia].
    Sulis E, Fiorelli G, Alessio L, Pabis A.
    Acta Haematol; 1968 Jan 03; 39(3):167-73. PubMed ID: 4970086
    [No Abstract] [Full Text] [Related]

  • 7. Anemia in patients with coinherited thalassemia and glucose-6-phosphate dehydrogenase deficiency.
    Pornprasert S, Phanthong S.
    Hemoglobin; 2013 Jan 03; 37(6):536-43. PubMed ID: 23944358
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  • 13. Hemoglobinopathies and glucose-6-phosphate dehydrogenase deficiency in one of the regions of Azerbaijan: mass screening and laboratory investigations.
    Javadov RB, Grinberg LN, Krasnova SN, Makhmudova SA, Troitskaya OV.
    Acta Biol Med Ger; 1977 Jan 03; 36(5-6):709-15. PubMed ID: 146387
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  • 14. [Congenital deficiency of intra-erythrocyte glucose-6-phosphate dehydrogenase in a subject affected by Cooley's disease].
    Tunioli AM.
    Riv Clin Pediatr; 1964 Nov 03; 74(5):257-65. PubMed ID: 5858279
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  • 17. Thalassemia phenotypes in Sardinia.
    Carcassi U, Cacace E, Mela Q, Passiu G, Perpignano G, Pintus A.
    Birth Defects Orig Artic Ser; 1982 Nov 03; 18(7):165-8. PubMed ID: 7159726
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  • 18. Glucose-6-phosphate dehydrogenase Toulouse. A new variant with marked instability and severe deficiency discovered in a family of Mediterranean ancestry.
    Vergnes H, Yoshida A, Gourdin D, Gherardi M, Biermé R, Ruffié J.
    Acta Haematol; 1974 Nov 03; 51(4):240-9. PubMed ID: 4152602
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  • 19. Genetic red cell abnormalities in Trengganu and Perlis (West Malaysia).
    Eng LI, McKay DA, Govindasamy S.
    Southeast Asian J Trop Med Public Health; 1971 Jun 03; 2(2):133-9. PubMed ID: 5002823
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