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PUBMED FOR HANDHELDS

Journal Abstract Search


160 related items for PubMed ID: 4112649

  • 1. Skeletal muscle glycogenosis type II: biochemical and electron microscopic investigations of one case.
    Canal N, Frattola L, Pellegrini G.
    Z Neurol; 1972; 201(2):98-108. PubMed ID: 4112649
    [No Abstract] [Full Text] [Related]

  • 2. Glycogen metabolism of human diploid fibroblast cells in culture. I. Studies of cells from patients with glycogenosis types II, 3, and V.
    DiMauro S, Rowland LP, Mellman WJ.
    Pediatr Res; 1973 Sep; 7(9):739-44. PubMed ID: 4200717
    [No Abstract] [Full Text] [Related]

  • 3. Lysosomal glycogen storage disease with normal acid maltase.
    Danon MJ, Oh SJ, DiMauro S, Manaligod JR, Eastwood A, Naidu S, Schliselfeld LH.
    Neurology; 1981 Jan; 31(1):51-7. PubMed ID: 6450334
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  • 6. [A vacuolar myopathy: autophagic glycogenosis of late onset. Ultrastructural study].
    Sengel A, Stoebner P, Isch F.
    Ann Anat Pathol (Paris); 1971 Jan; 16(1):47-54. PubMed ID: 5283285
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  • 7. Fine structure of skeletal muscle in type-3 glycogenosis.
    Neustein HB.
    Arch Pathol; 1969 Aug; 88(2):130-6. PubMed ID: 5256057
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  • 8. [Histochemical and ultrastructural study of a case of type 3 glycogenosis].
    Chamlian A, Mariani R, Lafon J, Adechy-Benkoel L, Mounition L.
    Ann Anat Pathol (Paris); 1971 Aug; 16(1):85-92. PubMed ID: 4327013
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  • 12. Autophagic glycogenosis of late onset with mitochondrial abnormalities: light and electron microscopic observations.
    Engel AG, Dale AJ.
    Mayo Clin Proc; 1968 Apr; 43(4):233-79. PubMed ID: 4886322
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  • 16. Myopathy resembling McArdle's syndrome.
    Slotwiner P, Song SK, Maker HS.
    Arch Neurol; 1969 Jun; 20(6):586-98. PubMed ID: 5253619
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  • 17. AN ELECTRON MICROSCOPIC AND BIOCHEMICAL STUDY OF TYPE II GLYCOGENOSIS.
    BAUDHUIN P, HERS HG, LOEB H.
    Lab Invest; 1964 Sep; 13():1139-52. PubMed ID: 14207888
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