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PUBMED FOR HANDHELDS

Journal Abstract Search


88 related items for PubMed ID: 118469

  • 21. Infantile acid maltase deficiency. III. Ultrastructure of metachromatic material and glycogen in muscle fibers.
    Griffin JL.
    Virchows Arch B Cell Pathol Incl Mol Pathol; 1984; 45(1):51-61. PubMed ID: 6199887
    [Abstract] [Full Text] [Related]

  • 22. The pathology of type II skeletal muscle glycogenosis. A light and electron-microscopic study.
    Hudgson P, Fulthorpe JJ.
    J Pathol; 1975 Jul; 116(3):139-47. PubMed ID: 172619
    [Abstract] [Full Text] [Related]

  • 23. [Involvement of vascular, mesenchymal and neural structures in a muscle of the patients with Pompe's disease (glycogenosis 2) (electron microscopic study)].
    Jadro-Santel D.
    Acta Med Iugosl; 1976 Mar; 30(2):203-14. PubMed ID: 1064289
    [No Abstract] [Full Text] [Related]

  • 24. Ultrastructure of the eye in fetal type II glycogenosis (Pompe's disease).
    Pokorny KS, Ritch R, Friedman AH, Desnick RJ.
    Invest Ophthalmol Vis Sci; 1982 Jan; 22(1):25-31. PubMed ID: 6948796
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  • 26. An autopsy case of type II glycogenosis.
    Asukata I, Aizawa S, Kosakai M, Kirino Y, Ishikawa E.
    Acta Pathol Jpn; 1976 Sep; 26(5):629-35. PubMed ID: 1069472
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  • 30. Vacuolated lymphocytes in type II glycogenosis--a diagnostic approach?
    von Bassewitz DB, Bremer HJ, Bourgeois M, Gröbe H, Stoermer J.
    Eur J Pediatr; 1977 Dec 30; 127(1):1-7. PubMed ID: 272287
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  • 31. [Generalized glycogenosis (Pompe's disease) in an 11-year-old girl].
    Rozenberg VD.
    Arkh Patol; 1978 Dec 30; 40(9):69-71. PubMed ID: 280283
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  • 33. [Congenital heart diseases].
    Okada R.
    Nihon Rinsho; 1979 Dec 30; 37(4):864-7. PubMed ID: 286818
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  • 34. Brain lysosomal enzymes in generalized gangliosidosis and metachromatic leukodystrophy.
    Den Tandt WR, Hooghwinkel GJ.
    Acta Neurol (Napoli); 1980 Feb 30; 2(1):10-4. PubMed ID: 6156575
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  • 36. [Lysosomal enzyme defects].
    Spranger J.
    Monatsschr Kinderheilkd; 1983 Jun 30; 131(6):311-7. PubMed ID: 6888383
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  • 37. Glycogen storage disease in Israel. A clinical, biochemical and genetic study.
    Levin S, Moses SW, Chayoth R, Jagoda N, Steinitz K.
    Isr J Med Sci; 1967 Jun 30; 3(3):397-410. PubMed ID: 5317551
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  • 39. [Enzyme deficiencies detected on cultured fibroblasts and amniotic cells. Application to prenatal diagnosis].
    Dreyfus JC, Poenaru L.
    Ann Biol Clin (Paris); 1975 Jun 30; 33(6):465-72. PubMed ID: 818927
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