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PUBMED FOR HANDHELDS

Journal Abstract Search


189 related items for PubMed ID: 15238150

  • 1. Dehydrated hereditary stomatocytosis is associated with neonatal hepatitis.
    Rees DC, Portmann B, Ball C, Mieli-Vergani G, Nicolaou A, Chetty MC, Stewart GW.
    Br J Haematol; 2004 Jul; 126(2):272-6. PubMed ID: 15238150
    [Abstract] [Full Text] [Related]

  • 2. Four pedigrees of the cation-leaky hereditary stomatocytosis class presenting with pseudohyperkalaemia. Novel profile of temperature dependence of Na+-K+ leak in a xerocytic form.
    Gore DM, Layton M, Sinha AK, Williamson PJ, Vaidya B, Connolly V, Mannix P, Chetty MC, Nicolaou A, Stewart GW.
    Br J Haematol; 2004 May; 125(4):521-7. PubMed ID: 15142123
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  • 4. [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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  • 7. Pseudohyperkalaemia and pseudomacrocytosis caused by inherited red-cell disorders of the 'hereditary stomatocytosis' group.
    Chetty MC, Stewart GW.
    Br J Biomed Sci; 2001 Jun; 58(1):48-55. PubMed ID: 11284226
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  • 9. Dehydrated hereditary stomatocytosis.
    Layton DM, Bain BJ.
    Am J Hematol; 2016 Feb; 91(2):266. PubMed ID: 26440377
    [No Abstract] [Full Text] [Related]

  • 10. Correction of the permeability defect in hereditary stomatocytosis by dimethyl adipimidate.
    Mentzer WC, Lubin BH, Emmons S.
    N Engl J Med; 1976 May 27; 294(22):1200-4. PubMed ID: 1264135
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  • 11. [A case of congenital stomatocytosis with normal sodium fluxes, normal enzyme activities of red cells, but with increased osmotic fragility of red cells].
    Kuratsuji T, Lee JY, Takahashi E, Shiro H, Yamada K, Miyashima K, Sugihara H, Yawata Y.
    Rinsho Ketsueki; 1986 Mar 27; 27(3):338-43. PubMed ID: 3016363
    [No Abstract] [Full Text] [Related]

  • 12. [A case of congenital stomatocytosis with decreased red cell sodium content, increased red cell sodium efflux and pulmonary embolism].
    Murai K, Yasunari K, Yasuda M, Negoro N, Yoshikawa C, Tatsumi J, Tatsumi N, Sugihara T, Shimoda M, Hashimoto M.
    Rinsho Ketsueki; 1985 May 27; 26(5):789-94. PubMed ID: 2997502
    [No Abstract] [Full Text] [Related]

  • 13. [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 27; 22(1):51-60. PubMed ID: 4592413
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  • 14. Hereditary dehydrated and overhydrated stomatocytosis: recent advances.
    Delaunay J, Stewart G, Iolascon A.
    Curr Opin Hematol; 1999 Mar 27; 6(2):110-4. PubMed ID: 10088641
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  • 15. [Congenital stomatocytosis associated with aplastic anemia].
    Takigawa A, Kajigaya Y, Funabiki T, Fukazawa K, Ikuta K, Sasaki H, Matsuyama S, Terasawa T, Shichishima T, Kanzaki A.
    Rinsho Ketsueki; 1989 May 27; 30(5):713-8. PubMed ID: 2795885
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  • 16. Abnormal permeability pathways in human red blood cells.
    Ellory JC, Robinson HC, Browning JA, Stewart GW, Gehl KA, Gibson JS.
    Blood Cells Mol Dis; 2007 May 27; 39(1):1-6. PubMed ID: 17434766
    [Abstract] [Full Text] [Related]

  • 17. Novel Gardos channel mutations linked to dehydrated hereditary stomatocytosis (xerocytosis).
    Andolfo I, Russo R, Manna F, Shmukler BE, Gambale A, Vitiello G, De Rosa G, Brugnara C, Alper SL, Snyder LM, Iolascon A.
    Am J Hematol; 2015 Oct 27; 90(10):921-6. PubMed ID: 26178367
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  • 18. The hereditary stomatocytoses and allied disorders: congenital disorders of erythrocyte membrane permeability to Na and K.
    Stewart GW, Turner EJ.
    Baillieres Best Pract Res Clin Haematol; 1999 Dec 27; 12(4):707-27. PubMed ID: 10895260
    [Abstract] [Full Text] [Related]

  • 19. [Congenital stomatocytosis associated with decreased sodium content in red cells].
    Masuda M, Kokago H, Oshimi K, Mizoguchi H, Hashimoto M, Kanzaki A, Yawata Y.
    Rinsho Ketsueki; 1987 Jun 27; 28(6):872-5. PubMed ID: 3669325
    [No Abstract] [Full Text] [Related]

  • 20. A novel erythroid anion exchange variant (Gly796Arg) of hereditary stomatocytosis associated with dyserythropoiesis.
    Iolascon A, De Falco L, Borgese F, Esposito MR, Avvisati RA, Izzo P, Piscopo C, Guizouarn H, Biondani A, Pantaleo A, De Franceschi L.
    Haematologica; 2009 Aug 27; 94(8):1049-59. PubMed ID: 19644137
    [Abstract] [Full Text] [Related]


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