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Journal Abstract Search

391 related items for PubMed ID: 448868

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  • 2. [Diagnosis of hereditary spherocytosis].
    Hermann J, Hetzinger S.
    Folia Haematol Int Mag Klin Morphol Blutforsch; 1989; 116(5):769-73. PubMed ID: 2481624
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  • 4. [Microspherocytosis. Erythroid profile and its relation with different laboratory tests].
    Aixála MT, Sarandría CN.
    Medicina (B Aires); 2001; 61(4):417-23. PubMed ID: 11563170
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  • 11. Variable clinical severity of hereditary spherocytosis: relation to erythrocytic spectrin concentration, osmotic fragility, and autohemolysis.
    Eber SW, Armbrust R, Schröter W.
    J Pediatr; 1990 Sep; 117(3):409-16. PubMed ID: 2391596
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  • 13. Diphenylhydantoin and fragility of erythrocytes in normal subjects and in patients with hereditary spherocytic anemia.
    Hansotia P, Mazza JJ, Gatlin P.
    Am J Clin Pathol; 1975 Jul; 64(1):75-9. PubMed ID: 1155377
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  • 15. Abnormality in a specific protein of the erythrocyte membrane in hereditary spherocytosis.
    Hayashi S, Koomoto R, Yano A, Ishigami S, Tsujino G.
    Biochem Biophys Res Commun; 1974 Apr 23; 57(4):1038-44. PubMed ID: 4830746
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  • 16. Glucose-induced hemolysis of spheric red blood cells in hereditary spherocytosis: new aspects of the autohemolysis test.
    Streichman S, Cohen S, Tatarsky I.
    Am J Clin Pathol; 1984 Jan 23; 81(1):122-7. PubMed ID: 6691298
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  • 18. Red blood cell aquaporin-1 expression is decreased in hereditary spherocytosis.
    Crisp RL, Maltaneri RE, Vittori DC, Solari L, Gammella D, Schvartzman G, García E, Rapetti MC, Donato H, Nesse A.
    Ann Hematol; 2016 Oct 23; 95(10):1595-601. PubMed ID: 27465156
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  • 20. The role of membrane lipids in the survival of red cells in hereditary spherocytosis.
    Cooper RA, Jandl JH.
    J Clin Invest; 1969 Apr 23; 48(4):736-44. PubMed ID: 5774111
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