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Journal Abstract Search

146 related items for PubMed ID: 285339

  • 1. McArdle disease: phosphorylase activity in regenerating muscle fibers.
    Mitsumoto H.
    Neurology; 1979 Feb; 29(2):258-62. PubMed ID: 285339
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  • 2. McArdle disease: the mysterious appearance of phosphorylase activity in cells that ought to lack the genetic program. A fetal isoenzyme?
    DiMauro S, Arnold S, Miranda A, Rowland LP.
    Trans Am Neurol Assoc; 1977 Feb; 102():112-5. PubMed ID: 278321
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  • 3. McArdle disease: the mystery of reappearing phosphorylase activity in muscle culture--a fetal isoenzyme.
    DiMauro S, Arnold S, Miranda A, Rowland LP.
    Ann Neurol; 1978 Jan; 3(1):60-6. PubMed ID: 418736
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  • 4. Characterization of glycogen phosphorylase isoenzymes present in cultured skeletal muscle from patients with McArdle's disease.
    Sato K, Imai F, Hatayama I, Roelofs RI.
    Biochem Biophys Res Commun; 1977 Sep 23; 78(2):663-8. PubMed ID: 269730
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  • 6. A new variant of late-onset myophosphorylase deficiency.
    Kost GJ, Verity MA.
    Muscle Nerve; 1980 Sep 23; 3(3):195-201. PubMed ID: 6929403
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  • 8. [Glycogenosis type V of adults: muscle phosphorylase deficiency].
    Coll Cantí J, Illa I, Beleta J, Anglada A, Pradas J, González Sastre F, Grau Veciana JM, Gella FJ.
    Med Clin (Barc); 1986 Mar 01; 86(8):335-8. PubMed ID: 3458989
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  • 10. Histochemical and biochemical studies in a patient with myophosphorylase deficiency.
    Tachi N, Sasaki K, Tachi M, Sugie H.
    Eur Neurol; 1990 Mar 01; 30(1):52-5. PubMed ID: 2298228
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  • 11. [Morphological and biochemical studies on glycogenosis type V (McArdle) (author's transl)].
    Pongratz D, Schaub J, Koppenwallner C, Hübner G.
    Klin Wochenschr; 1981 Sep 15; 59(18):1053-9. PubMed ID: 6795385
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  • 12. Sodium valproate increases the brain isoform of glycogen phosphorylase: looking for a compensation mechanism in McArdle disease using a mouse primary skeletal-muscle culture in vitro.
    de Luna N, Brull A, Guiu JM, Lucia A, Martin MA, Arenas J, Martí R, Andreu AL, Pinós T.
    Dis Model Mech; 2015 May 15; 8(5):467-72. PubMed ID: 25762569
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  • 13. Phosphorylase re-expression, increase in the force of contraction and decreased fatigue following notexin-induced muscle damage and regeneration in the ovine model of McArdle disease.
    Howell JM, Walker KR, Creed KE, Dunton E, Davies L, Quinlivan R, Karpati G.
    Neuromuscul Disord; 2014 Feb 15; 24(2):167-77. PubMed ID: 24309536
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  • 14. In McArdle disease, phosphorylase deficiency is the tip of an iceberg.
    Willner JH, Cerri CG, Wood DS, Ponzetto-Zimmerman C, Reydel PM.
    Trans Am Neurol Assoc; 1981 Feb 15; 106():208-9. PubMed ID: 6294950
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  • 16. Adenovirus-mediated delivery into myocytes of muscle glycogen phosphorylase, the enzyme deficient in patients with glycogen-storage disease type V.
    Baqué S, Newgard CB, Gerard RD, Guinovart JJ, Gómez-Foix AM.
    Biochem J; 1994 Dec 15; 304 ( Pt 3)(Pt 3):1009-14. PubMed ID: 7818463
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  • 17. Research on molecular mechanisms of McArdle's disease (muscle glycogen phosphorylase deficiency). Use of new protein mapping and immunological techniques.
    Daegelen-Proux D, Kahn A, Marie J, Dreyfus JC.
    Ann Hum Genet; 1981 May 15; 45(2):113-20. PubMed ID: 6797345
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