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Journal Abstract Search

324 related items for PubMed ID: 15142658

  • 1. A basis of the acanthocytosis in inherited and acquired disorders.
    Wong P.
    Med Hypotheses; 2004; 62(6):966-9. PubMed ID: 15142658
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  • 2. A basis of echinocytosis and stomatocytosis in the disc-sphere transformations of the erythrocyte.
    Wong P.
    J Theor Biol; 1999 Feb 07; 196(3):343-61. PubMed ID: 10049626
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  • 3. The behavior of the human erythrocyte as an imperfect osmometer: a hypothesis.
    Wong P.
    J Theor Biol; 2006 Jan 07; 238(1):167-71. PubMed ID: 16038940
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  • 4. Red cell deformability and lipid composition in two forms of acanthocytosis: enrichment of acanthocytic populations by density gradient centrifugation.
    Clark MR, Aminoff MJ, Chiu DT, Kuypers FA, Friend DS.
    J Lab Clin Med; 1989 Apr 07; 113(4):469-81. PubMed ID: 2703759
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  • 5. Mechanism of control of erythrocyte shape: a possible relationship to band 3.
    Wong P.
    J Theor Biol; 1994 Nov 21; 171(2):197-205. PubMed ID: 7844997
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  • 15. Erythrocyte anion transporter and antibrain immunoreactivity in chorea-acanthocytosis. A contribution to etiology, genetics, and diagnosis.
    Bosman GJ, Bartholomeus IG, De Grip WJ, Horstink MW.
    Brain Res Bull; 1994 Nov 21; 33(5):523-8. PubMed ID: 8186997
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  • 16. [Reversible acquired acanthocytosis and hemolytic anemia associated with hypobetalipoproteinemia in a chronic alcoholic].
    Beris P, Suenram A, Pometta D, Miescher PA.
    Schweiz Med Wochenschr; 1983 Oct 08; 113(40):1473-5. PubMed ID: 6417778
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  • 17. Acanthocytosis and neurological impairment--a review.
    Hardie RJ.
    Q J Med; 1989 Apr 08; 71(264):291-306. PubMed ID: 2687930
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  • 19. Chorea-acanthocytosis: a report of three new families and implications for genetic counselling.
    Vance JM, Pericak-Vance MA, Bowman MH, Payne CS, Fredane L, Siddique T, Roses AD, Massey EW.
    Am J Med Genet; 1987 Oct 08; 28(2):403-10. PubMed ID: 3322006
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  • 20. Band 3 HT, a human red-cell variant associated with acanthocytosis and increased anion transport, carries the mutation Pro-868-->Leu in the membrane domain of band 3.
    Bruce LJ, Kay MM, Lawrence C, Tanner MJ.
    Biochem J; 1993 Jul 15; 293 ( Pt 2)(Pt 2):317-20. PubMed ID: 8343110
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