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Journal Abstract Search

131 related items for PubMed ID: 1066528

  • 1.
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  • 2. McArdle's disease: a study on the molecular basis of two different etiologies of myophosphorylase deficiency.
    Koster JF, Slee RG, Jennekens FG, Wintzen AR, van Berkel TJ.
    Clin Chim Acta; 1979 Jun 15; 94(3):229-35. PubMed ID: 111879
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  • 5. 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 Jun 15; 106():208-9. PubMed ID: 6294950
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  • 6. 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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  • 7. [McArdle's disease (muscular phosphorylase deficiency)].
    Schollmeyer P, Nolte J, Meisel D, Dichgans J, Jerusalem F.
    Verh Dtsch Ges Inn Med; 1981 May 15; 83():1277-80. PubMed ID: 274025
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  • 8. Low muscle levels of pyridoxine in McArdle's syndrome.
    Haller RG, Dempsey WB, Feit H, Cook JD, Knochel JP.
    Am J Med; 1983 Feb 15; 74(2):217-20. PubMed ID: 6572033
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  • 9. McArdle's disease--what limit to the age of onset?
    Hewlett RH, Gardner-Thorpe C.
    S Afr Med J; 1978 Jan 14; 53(2):60-3. PubMed ID: 273990
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  • 10. Angina in McArdle's disease.
    Nicholls DP, Campbell NP, Stevenson HP, Patterson VH.
    Heart; 1996 Oct 14; 76(4):372-3. PubMed ID: 8983689
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  • 11. Expression of muscle-type phosphorylase in innervated and aneural cultured muscle of patients with myophosphorylase deficiency.
    Martinuzzi A, Vergani L, Carrozzo R, Fanin M, Bartoloni L, Angelini C, Askanas V, Engel WK.
    J Clin Invest; 1993 Oct 14; 92(4):1774-80. PubMed ID: 8408630
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  • 12. Phosphorylase isoenzymes in normal and myophosphorylase-deficient human heart.
    Miranda AF, Nette EG, Hartlage PL, DiMauro S.
    Neurology; 1979 Nov 14; 29(11):1538-41. PubMed ID: 291791
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  • 13. 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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  • 14. McArdle's syndrome. Fine structural changes in muscle.
    Korényi-Both A, Smith BH, Baruah JK.
    Acta Neuropathol; 1977 Sep 26; 40(1):11-9. PubMed ID: 269622
    [Abstract] [Full Text] [Related]

  • 15. McArdle's disease presenting as treatment resistant polymyositis.
    Higgs JB, Blaivas M, Albers JW.
    J Rheumatol; 1989 Dec 26; 16(12):1588-91. PubMed ID: 2625691
    [Abstract] [Full Text] [Related]

  • 16. Absence of functional messenger RNA for glycogen phosphorylase in the muscle of two patients with McArdle's disease.
    Daegelen D, Munnich A, Levin MJ, Girault A, Goasguen J, Kahn A, Dreyfus JC.
    Ann Hum Genet; 1983 May 26; 47(2):107-15. PubMed ID: 6576726
    [Abstract] [Full Text] [Related]

  • 17. A new variant of late-onset myophosphorylase deficiency.
    Kost GJ, Verity MA.
    Muscle Nerve; 1980 May 26; 3(3):195-201. PubMed ID: 6929403
    [Abstract] [Full Text] [Related]

  • 18. Phosphorylation of McArdle phosphorylase induces activity.
    Cerri CG, Willner JH.
    Proc Natl Acad Sci U S A; 1981 May 26; 78(5):2688-92. PubMed ID: 6265901
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  • 19. Molecular mechanisms of McArdle's disease (muscle glycogen phosphorylase deficiency). RNA and DNA analysis.
    Gautron S, Daegelen D, Mennecier F, Dubocq D, Kahn A, Dreyfus JC.
    J Clin Invest; 1987 Jan 26; 79(1):275-81. PubMed ID: 3466902
    [Abstract] [Full Text] [Related]

  • 20. A female case of glycogen storage myopathy due to phosphorylase kinase deficiency.
    Ohtani Y, Matsuda I, Iwamasa T.
    J Inherit Metab Dis; 1982 Jan 26; 5(2):71-2. PubMed ID: 6820425
    [No Abstract] [Full Text] [Related]

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