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Journal Abstract Search

125 related items for PubMed ID: 6797345

  • 1. 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; 45(2):113-20. PubMed ID: 6797345
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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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  • 3. Myophosphorylase deficiency: two different molecular etiologies.
    Feit H, Brooke MH.
    Neurology; 1976 Oct 15; 26(10):963-7. PubMed ID: 1066528
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  • 4. Molecular heterogeneity in McArdle's disease.
    McConchie SM, Coakley J, Edwards RH, Beynon RJ.
    Biochim Biophys Acta; 1990 Nov 14; 1096(1):26-32. PubMed ID: 2268682
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  • 5. Absence of biochemical heterogeneity in McArdle's disease. A high resolution SDS-polyacrylamide gel electrophoresis study.
    Mantle D, Lauffart B, Atack J, Lane RJ.
    J Neurol Sci; 1987 Mar 14; 78(1):63-70. PubMed ID: 3471865
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  • 11. 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. 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 14; 3(1):60-6. PubMed ID: 418736
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  • 14. 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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  • 19. McArdle's disease: biochemical and molecular genetic studies.
    Servidei S, Shanske S, Zeviani M, Lebo R, Fletterick R, DiMauro S.
    Ann Neurol; 1988 Dec 14; 24(6):774-81. PubMed ID: 3207360
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