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Journal Abstract Search

129 related items for PubMed ID: 10050708

  • 1. 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]

  • 2. 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]

  • 3. 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]

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

  • 5. 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; 105(4):1055-65. PubMed ID: 10554820
    [Abstract] [Full Text] [Related]

  • 6. 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]

  • 7. Two further British families with the 'cryohydrocytosis' form of hereditary stomatocytosis.
    Haines PG, Jarvis HG, King S, Noormohamed FH, Chetty MC, Fisher J, Hill P, Nicolaou A, Stewart GW.
    Br J Haematol; 2001 Jun; 113(4):932-7. PubMed ID: 11442486
    [Abstract] [Full Text] [Related]

  • 8. A genetic syndrome associating dehydrated hereditary stomatocytosis, pseudohyperkalaemia and perinatal oedema.
    Grootenboer S, Schischmanoff PO, Cynober T, Rodrigue JC, Delaunay J, Tchernia G, Dommergues JP.
    Br J Haematol; 1998 Nov; 103(2):383-6. PubMed ID: 9827909
    [Abstract] [Full Text] [Related]

  • 9. Pseudohyperkalaemia and pseudomacrocytosis caused by inherited red-cell disorders of the 'hereditary stomatocytosis' group.
    Chetty MC, Stewart GW.
    Br J Biomed Sci; 2001 Nov; 58(1):48-55. PubMed ID: 11284226
    [Abstract] [Full Text] [Related]

  • 10. The hereditary stomatocytoses: genetic disorders of the red cell membrane permeability to monovalent cations.
    Delaunay J.
    Semin Hematol; 2004 Apr; 41(2):165-72. PubMed ID: 15071792
    [Abstract] [Full Text] [Related]

  • 11. 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]

  • 12. 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 01; 152(5):655-64. PubMed ID: 21255002
    [Abstract] [Full Text] [Related]

  • 13. A family with mild hereditary xerocytosis showing high membrane cation permeability at low temperatures.
    Stewart GW, Ellory JC.
    Clin Sci (Lond); 1985 Sep 01; 69(3):309-19. PubMed ID: 4064573
    [Abstract] [Full Text] [Related]

  • 14. The curious genomic path from leaky red cell to nephrotic kidney.
    Stewart GW, Fricke B.
    Nephron Physiol; 2003 Sep 01; 93(2):p29-33. PubMed ID: 12629268
    [Abstract] [Full Text] [Related]

  • 15. 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]

  • 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. Temperature sensitivity of potassium flux into red blood cells in the familial pseudohyperkalaemia syndrome.
    Meenaghan M, Follett GF, Brophy PJ.
    Biochim Biophys Acta; 1985 Nov 21; 821(1):72-8. PubMed ID: 2998465
    [Abstract] [Full Text] [Related]

  • 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 21; 12(4):707-27. PubMed ID: 10895260
    [Abstract] [Full Text] [Related]

  • 19. 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 21; 126(2):272-6. PubMed ID: 15238150
    [Abstract] [Full Text] [Related]

  • 20. Familial pseudohyperkalaemia: inhibition of erythrocyte K+ efflux at 4 degrees C by quinine.
    James DR, Stansbie D.
    Clin Sci (Lond); 1987 Nov 21; 73(5):557-60. PubMed ID: 3677562
    [Abstract] [Full Text] [Related]

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