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Journal Abstract Search

94 related items for PubMed ID: 11442486

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  • 2. 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
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  • 3. 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
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  • 5. 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
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  • 9. Dehydrated hereditary stomatocytosis--a report of two families and a review of the literature.
    McGrath KM, Collecutt MF, Gordon A, Sawers RJ, Faragher BS.
    Pathology; 1984 Apr; 16(2):146-50. PubMed ID: 6462777
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  • 11. A family of hereditary stomatocytosis associated with normal level of Na+-K+-ATPase activity of red blood cells.
    Mutoh S, Sasaki R, Takaku F, Aoyama M, Moriyama S, Yoshimoto M, Yawata Y.
    Am J Hematol; 1983 Apr; 14(2):113-20. PubMed ID: 6301265
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  • 12. The nonspherocytic congenital haemolytic anaemias.
    de Gruchy GC, Grimes AJ.
    Br J Haematol; 1972 Sep; 23():Suppl:19-26. PubMed ID: 4567191
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  • 18. Evaluation by continuously recording hypotonic hemolysis of various normal and pathological erythrocytes.
    Shields CE, Allen TE, Fogel BJ.
    Am J Med Sci; 1966 Jun; 251(6):656-63. PubMed ID: 5946365
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  • 20. A novel stomatocytosis variant showing marked abnormalities in intracellular [Na] and [K] with minimal haemolysis.
    Jarvis HG, Chetty MC, Nicolaou A, Fisher J, Miller A, Stewart GW.
    Eur J Haematol; 2001 Jun; 66(6):412-4. PubMed ID: 11488942
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