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PUBMED FOR HANDHELDS

Journal Abstract Search


169 related items for PubMed ID: 5559828

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  • 4. Hereditary stomatocytosis with hemolytic anemia in the dog.
    Pinkerton PH, Fletch SM, Brueckner PJ, Miller DR.
    Blood; 1974 Oct; 44(4):557-67. PubMed ID: 4278122
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  • 5. [Congenital hemolytic anemia with spherocytosis and erythrocyte cation abnormalities].
    Bernard JF, Afifi F, Hakim J, Boivin P.
    Nouv Rev Fr Hematol; 1974 Oct; 14(4):439-52. PubMed ID: 4280554
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  • 6. Hemoglobin Köln disease occurring as a fresh mutation: erythrocyte metabolism and survival.
    Miller DR, Weed RI, Stamatoyannopoulos G, Yoshida A.
    Blood; 1971 Dec; 38(6):715-29. PubMed ID: 4942314
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  • 7. [Hereditary stomatocytosis of the hydrocytosis type: a report of one family and red cell membrane studies].
    Kida T, Nakamura H, Kuroki T, Mizoguchi Y, Kobayashi K, Yamane T, Im T, Tatsumi N, Ata K, Wada H.
    Rinsho Ketsueki; 1990 Jun; 31(6):813-9. PubMed ID: 2170705
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  • 11. Glutathione synthetase deficiency as a cause of hereditary hemolytic disease.
    Mohler DN, Majerus PW, Minnich V, Hess CE, Garrick MD.
    N Engl J Med; 1970 Dec 03; 283(23):1253-7. PubMed ID: 5476481
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  • 14. Variant type of congenital stomatocytosis.
    Morita H, Wada H, Tsujinoue H, Kurioka T, Ueno Y, Shichikawa K, Amano H, Higo I, Kanzaki A, Yawata Y.
    Intern Med; 1994 Feb 03; 33(2):103-6. PubMed ID: 8019039
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  • 18. [Congenital stomatocytosis with hemolytic anemia--with abnormal cation permeability and defective membrane proteins].
    Rix M, Bjerrum PJ, Wieth JO, Frandsen B.
    Ugeskr Laeger; 1991 Mar 04; 153(10):724-6. PubMed ID: 2008721
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  • 19. [Na and K cation levels and exchange across the membrane of the erythrocyte. II. Results obtained in the erythrocytes of 20 patients with congenital hemolytic anemia].
    Bernard JF, Afifi F, Boivin P.
    Pathol Biol (Paris); 1974 Jan 04; 22(1):51-60. PubMed ID: 4592413
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  • 20. The membrane defect in hereditary stomatocytosis.
    Stewart GW.
    Baillieres Clin Haematol; 1993 Jun 04; 6(2):371-99. PubMed ID: 8043931
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