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Journal Abstract Search

126 related items for PubMed ID: 13905912

  • 1. [Hemolytic anemia induced by a sulfonamide in the presence of a glucose-6-phosphate-dehydrogenase deficiency, a hetero-chromosomal hereditary disease].
    HEERES PA, ZONDAG HA.
    Sem Hop; 1961 Dec 30; 37():3666-70. PubMed ID: 13905912
    [No Abstract] [Full Text] [Related]

  • 2. [Hemolytic anemia caused by sulfanilamide as a result of glucose-6-phosphate-dehydrogenase deficiency: an x-chromosomal hereditary disease].
    HEERES PA, ZONDAG HA.
    Folia Med Neerl; 1961 Jul 30; 4():121-31. PubMed ID: 13905911
    [No Abstract] [Full Text] [Related]

  • 3. The hemolytic effect of various sulfonamides on subjects with a deficiency of glucose-6-phosphate dehydrogenase of erythrocytes.
    SZEINBERG A, PRAS M, SHEBA C, ADAM A, RAMOT B.
    Isr Med J; 1959 Jul 30; 18():176-83. PubMed ID: 13836343
    [No Abstract] [Full Text] [Related]

  • 4. [Hemolytic anemia due to congenital glucose-6-phosphate dehydrogenase deficiency].
    NEIMANN N, DUCAS J.
    Pediatrie; 1960 Jul 30; 15():391-405. PubMed ID: 14426390
    [No Abstract] [Full Text] [Related]

  • 5. CHRONIC HEMOLYSIS ASSOCIATED WITH GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY.
    BEN-ISHAY D, IZAK G.
    J Lab Clin Med; 1964 Jun 30; 63():1002-9. PubMed ID: 14179116
    [No Abstract] [Full Text] [Related]

  • 6. [On congenital hemolytic, nonspherocytic anemias with a deficiency of glucose-6-phosphate dehydrogenase in red blood cells].
    GHIOTTO G, PERONA G, DE SANDRE G.
    Folia Haematol Int Mag Klin Morphol Blutforsch; 1962 Jun 30; 78():639-45. PubMed ID: 13898200
    [No Abstract] [Full Text] [Related]

  • 7. The existence of the glucose-6-phosphate dehydrogenase deficiency trait in Nigeria and its clinical implications.
    GILLES HM, TAYLOR BG.
    Ann Trop Med Parasitol; 1961 Apr 30; 55():64-9. PubMed ID: 13705322
    [No Abstract] [Full Text] [Related]

  • 8. Glucose-6-phosphate dehydrogenase deficiency in congenital hemolytic disease. A review.
    FREDRICK EE.
    J Natl Med Assoc; 1962 Sep 30; 54(5):576-83. PubMed ID: 13894838
    [No Abstract] [Full Text] [Related]

  • 9. Haemolytic jaundice following aspirin administration to a patient with a deficiency of glucose-6-phosphate dehydrogenase in erythrocytes.
    SZEINBERG A, KELLERMANN J, ADAM A, SHEBA C, RAMOT B.
    Acta Haematol; 1960 Jan 30; 23():58-64. PubMed ID: 13836342
    [No Abstract] [Full Text] [Related]

  • 10. [HEMOLYTIC ANEMIAS DUE TO HEREDITARY DEFECT OF GLUCOSE-6-PHOSPHATE-DEHYDROGENASE].
    RICOIRLES J.
    Rev Clin Esp; 1964 Jan 31; 92():77-87. PubMed ID: 14111194
    [No Abstract] [Full Text] [Related]

  • 11. Glucose-6-phosphate dehydrogenase deficiency in red cells.
    BAILEY IS, DE LOECKER WC, PRANKERD TA.
    Z Gesamte Exp Med; 1961 Jan 31; 134():260-7. PubMed ID: 13685953
    [No Abstract] [Full Text] [Related]

  • 12. [RESEARCH ON GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY IN FRANCE. APROPOS OF 200 DETERMINATIONS].
    DREYFUS JC, MALEKNIA N, KAPLAN JC.
    Nouv Rev Fr Hematol; 1964 Jan 31; 4():791-802. PubMed ID: 14233376
    [No Abstract] [Full Text] [Related]

  • 13. [ACUTE HEMOLYTIC ANEMIA CAUSED BY NITROFURANTOIN IN AN IRANIAN WOMAN PRESENTING AN ERYTHROCYTE GLUCOSE-6-PHOSPHATE-DEHYDROGENASE DEFICIENCY; DEMONSTRATION OF THE HETEROZYGOSIS OF THE PATIENT BY AN ORIGINAL METHOD].
    JEANNET M, PERRIER CV, TOENZ O.
    Schweiz Med Wochenschr; 1964 Jun 27; 94():939-43. PubMed ID: 14238354
    [No Abstract] [Full Text] [Related]

  • 14. [STUDIES ON ERYTHROCYTES OF A GLUCOSE-6-PHOSPHATE-NADP-OXIDOREDUCTASE DEFECT].
    SCHEUCH D.
    Folia Haematol Int Mag Klin Morphol Blutforsch; 1964 Jun 27; 82():76-85. PubMed ID: 14253329
    [No Abstract] [Full Text] [Related]

  • 15. [Hemolytic erythrocytopathy caused by absence of glucose-6-phosphate dehydrogenase in red cells as a dominant hereditary factor].
    LOHR GW, WALLER HD.
    Klin Wochenschr; 1958 Sep 15; 36(18):865-9. PubMed ID: 13588927
    [No Abstract] [Full Text] [Related]

  • 16. Glucose-6-phosphate dehydrogenase deficiency. A new aetiological factor of severe neonatal jaundice.
    DOXIADIS SA, FESSAS P, VALAES T.
    Lancet; 1961 Feb 11; 1(7172):297-301. PubMed ID: 13724172
    [No Abstract] [Full Text] [Related]

  • 17. [THE CLINICAL SIGNIFICANCE OF HEREDITARY GLUCOSE-6-PHOSPHATE-DEHYDROGENASE INACTIVITY].
    FLATZ G.
    Med Klin; 1964 Apr 24; 59():687-91. PubMed ID: 14213623
    [No Abstract] [Full Text] [Related]

  • 18. Neonatal jaundice: two cases associated with glucose-6-phosphate dehydrogenase deficiency in erythrocytes.
    LEE C, TINK A, ROBIN H, HARLEY J.
    Med J Aust; 1961 Aug 19; 48(2)():315-8. PubMed ID: 13760218
    [No Abstract] [Full Text] [Related]

  • 19. Glucose-6-phosphate dehydrogenase dye test on patients and their family members of acute hemolytic anemia.
    SHIH LY, LEE TC.
    Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi; 1961 Aug 19; 2():106-12. PubMed ID: 13911883
    [No Abstract] [Full Text] [Related]

  • 20. [Hemolytic anemia caused by nitrofurazone revealing a globular deficiency in glucose-6-phosphate-dehydrogenase].
    SONNET J, VANDEPITTE J, HAUMONT A.
    Ann Soc Belg Med Trop (1920); 1959 Oct 31; 39():691-701. PubMed ID: 13832832
    [No Abstract] [Full Text] [Related]

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