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Journal Abstract Search

170 related items for PubMed ID: 15142123

  • 1. 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
    [Abstract] [Full Text] [Related]

  • 2. Familial pseudohyperkalaemia Chiswick: a novel congenital thermotropic variant of K and Na transport across the human red cell membrane.
    Haines PG, Crawley C, Chetty MC, Jarvis H, Coles SE, Fisher J, Nicolaou A, Stewart GW.
    Br J Haematol; 2001 Feb; 112(2):469-74. PubMed ID: 11167849
    [Abstract] [Full Text] [Related]

  • 3. Four new cases of stomatin-deficient hereditary stomatocytosis syndrome: association of the stomatin-deficient cryohydrocytosis variant with neurological dysfunction.
    Fricke B, Jarvis HG, Reid CD, Aguilar-Martinez P, Robert A, Quittet P, Chetty M, Pizzey A, Cynober T, Lande WF, Mentzer WC, Düring M, Winter S, Delaunay J, Stewart GW.
    Br J Haematol; 2004 Jun; 125(6):796-803. PubMed ID: 15180870
    [Abstract] [Full Text] [Related]

  • 4. 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
    [Abstract] [Full Text] [Related]

  • 5. South-east Asian ovalocytosis and the cryohydrocytosis form of hereditary stomatocytosis show virtually indistinguishable cation permeability defects.
    Guizouarn H, Borgese F, Gabillat N, Harrison P, Goede JS, McMahon C, Stewart GW, Bruce LJ.
    Br J Haematol; 2011 Mar; 152(5):655-64. PubMed ID: 21255002
    [Abstract] [Full Text] [Related]

  • 6. A variant of hereditary stomatocytosis with marked pseudohyperkalaemia.
    Coles SE, Ho MM, Chetty MC, Nicolaou A, Stewart GW.
    Br J Haematol; 1999 Feb; 104(2):275-83. PubMed ID: 10050708
    [Abstract] [Full Text] [Related]

  • 7. 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]

  • 8. Familial pseudohyperkalaemia Cardiff: a mild version of cryohydrocytosis.
    Gore DM, Chetty MC, Fisher J, Nicolaou A, Stewart GW.
    Br J Haematol; 2002 Apr; 117(1):212-4. PubMed ID: 11918557
    [Abstract] [Full Text] [Related]

  • 9. Hereditary stomatocytosis and cation-leaky red cells--recent developments.
    Bruce LJ.
    Blood Cells Mol Dis; 2009 Apr; 42(3):216-22. PubMed ID: 19261491
    [Abstract] [Full Text] [Related]

  • 10. [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
    [Abstract] [Full Text] [Related]

  • 11. Temperature effects on cation transport in hereditary stomatocytosis and allied disorders.
    Coles SE, Stewart GW.
    Int J Exp Pathol; 1999 Oct 04; 80(5):251-8. PubMed ID: 10607015
    [Abstract] [Full Text] [Related]

  • 12. A family with mild hereditary xerocytosis showing high membrane cation permeability at low temperatures.
    Stewart GW, Ellory JC.
    Clin Sci (Lond); 1985 Sep 04; 69(3):309-19. PubMed ID: 4064573
    [Abstract] [Full Text] [Related]

  • 13. Two British families with variants of the 'cryohydrocytosis' form of hereditary stomatocytosis.
    Coles SE, Chetty MC, Ho MM, Nicolaou A, Kearney JW, Wright SD, Stewart GW.
    Br J Haematol; 1999 Jun 04; 105(4):1055-65. PubMed ID: 10554820
    [Abstract] [Full Text] [Related]

  • 14. Familial pseudohyperkalemia maps to the same locus as dehydrated hereditary stomatocytosis (hereditary xerocytosis).
    Iolascon A, Stewart GW, Ajetunmobi JF, Perrotta S, Delaunay J, Carella M, Zelante L, Gasparini P.
    Blood; 1999 May 01; 93(9):3120-3. PubMed ID: 10216110
    [Abstract] [Full Text] [Related]

  • 15. [Pseudohyperkalemia of erythrocyte origin. Passive increase of membrane permeability to potassium].
    Enet-Renou N, Mirouze J, Dagher G, Dupont M, Richard JL, Mimran A.
    Pathol Biol (Paris); 1983 Sep 01; 31(7):583-8. PubMed ID: 6355987
    [Abstract] [Full Text] [Related]

  • 16. Leaky cell syndrome: a rare cause of pseudohyperkalaemia.
    Lukens MV, de Mare A, Kerbert-Dreteler MJ, van den Bergh FA.
    Ann Clin Biochem; 2012 Jan 01; 49(Pt 1):97-100. PubMed ID: 22042978
    [Abstract] [Full Text] [Related]

  • 17. Altered erythrocyte cation permeability in familial pseudohyperkalaemia.
    Dagher G, Vantyghem MC, Doise B, Lallau G, Racadot A, Lefebvre J.
    Clin Sci (Lond); 1989 Aug 01; 77(2):213-6. PubMed ID: 2766660
    [Abstract] [Full Text] [Related]

  • 18. [Genetic diseases of erythrocyte membrane permeability].
    Delaunay J.
    Ann Biol Clin (Paris); 1999 Aug 01; 57(4):383-91. PubMed ID: 10432360
    [Abstract] [Full Text] [Related]

  • 19. 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 01; 12(4):707-27. PubMed ID: 10895260
    [Abstract] [Full Text] [Related]

  • 20. Hereditary stomatocytosis: association of low 2,3-diphosphoglycerate with increased cation pumping by the red cell.
    Wiley JS, Cooper RA, Adachi K, Asakura T.
    Br J Haematol; 1979 Jan 01; 41(1):133-41. PubMed ID: 420735
    [Abstract] [Full Text] [Related]

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