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PUBMED FOR HANDHELDS

Journal Abstract Search


140 related items for PubMed ID: 7410551

  • 1. Myotonic muscular dystrophy: defective phospholipid metabolism in the erythrocyte plasma membrane.
    Grey JE, Gitelman HJ, Roses AD.
    J Clin Invest; 1980 Jun; 65(6):1478-82. PubMed ID: 7410551
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  • 2. Myotonic dystrophy: calcium-dependent phosphatidic acid synthesis in erythrocytes.
    Moore RB, Appel SH, Plishker GA.
    Ann Neurol; 1981 Nov; 10(5):491-3. PubMed ID: 7305303
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  • 4. Study on the erythrocytes from myotonic dystrophy with multi-nuclear NMR.
    Kuwabara T, Yuasa T, Ohno T, Yamamuro M, Miyatake T.
    Muscle Nerve; 1991 Jan; 14(1):57-63. PubMed ID: 1992297
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  • 7. Red blood cell alterations in muscular dystrophy: the role of lipids.
    Plishker GA, Appel SH.
    Muscle Nerve; 1980 Jan; 3(1):70-81. PubMed ID: 6246420
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  • 8. Altered component a phosphorylation in erythrocyte membranes in myotonic muscular dystrophy.
    Wong P, Roses AD.
    Prog Clin Biol Res; 1978 Jan; 21():479-91. PubMed ID: 662903
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  • 10. Methylation of erythrocyte membrane phospholipid in patients with early-onset myotonic dystrophy.
    Eda I, Takeshita K.
    Brain Dev; 1984 Jan; 6(3):284-8. PubMed ID: 6486376
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  • 11. The membrane lipid and fatty acid composition of erythrocyte ghosts from three patients with paramyotonia congenita.
    Marx A, Szymanska G, Melzner I, Rüdel R.
    Muscle Nerve; 1988 May; 11(5):471-7. PubMed ID: 3374519
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  • 13. [The effect of membrane-bound calcium on the activity of adenosine triphosphatase from erythrocytes and erythrocyte permeability for monovalent cations].
    Orlov SN, Shevchenko AS.
    Biokhimiia; 1978 Feb; 43(2):208-15. PubMed ID: 148300
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  • 14. Comment on erythrocyte phospholipid metabolism in myotonic muscular dystrophy.
    Grey J, Gitelman H, Roses AD.
    Ann Neurol; 1981 Nov; 10(5):494. PubMed ID: 7305304
    [No Abstract] [Full Text] [Related]

  • 15. Active calcium transport in normal and abnormal human erythrocytes.
    Al-Jobore A, Minocherhomjee AM, Villalobo A, Roufogalis BD.
    Prog Clin Biol Res; 1984 Nov; 159():243-92. PubMed ID: 6236466
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  • 16. Myotonic dystrophy: fragility of band 3 membrane protein upon resealing of erythrocyte ghosts and the normality of ATPase activity, sialic acid content, and spectrin extractability of ghosts.
    Tsuchiya Y, Sugita H, Kuroiwa Y.
    Biochem Med; 1983 Dec; 30(3):271-9. PubMed ID: 6228227
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  • 17. In vitro studies on calcium activated phosphatidylinositol phosphodiesterase of erythrocyte ghosts from normal individuals and those with myotonic muscular dystrophy.
    Meredith AL, Harper PS, Bradley DM.
    Clin Chim Acta; 1982 Apr 08; 120(2):201-6. PubMed ID: 6279336
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  • 18. The sialic acid and galactose concentrations in erythrocyte membranes in patients with myotonic dystrophy, limb-girdle and facioscapulohumeral dystrophy.
    Stibler H, Sydow O.
    J Neurol Sci; 1983 Jun 08; 59(3):389-99. PubMed ID: 6875606
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  • 19. Electron spin resonance investigations of membrane proteins in erythrocytes in muscle diseases. Duchenne and myotonic muscular dystrophy and congenital myotonia.
    Butterfield DA.
    Biochim Biophys Acta; 1977 Oct 03; 470(1):1-7. PubMed ID: 197998
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  • 20. Spin-label studies of erythrocytes in myotonic dystrophy: no increase in membrane fluidity.
    Gaffney BJ, Drachman DB, Lin DC, Tennekoon G.
    Neurology; 1980 Mar 03; 30(3):272-6. PubMed ID: 7189026
    [Abstract] [Full Text] [Related]


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