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Journal Abstract Search

231 related items for PubMed ID: 58976

  • 1. The symptomatology, morphology and biochemistry of glycogenosis type II (Pompe) in the adult.
    Schlenska GK, Heene R, Spalke G, Seiler D.
    J Neurol; 1976 Jun 14; 212(3):237-52. PubMed ID: 58976
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  • 2. An especially mild myopathic form of glycogenosis type II. Problems of clinical and light microscopic diagnosis.
    Pongratz D, Schlossmacher I, Koppenwallner C, Hübner G.
    Pathol Eur; 1976 Jun 14; 11(1):39-44. PubMed ID: 132627
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  • 3. Muscular form of glycogenosis type II (Pompe's disease).
    Tanaka K, Shimazu S, Oya N, Tomisawa M, Kusunoki T, Soyama K, Ono E.
    Pediatrics; 1979 Jan 14; 63(1):124-9. PubMed ID: 375166
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  • 8. Uncommon case of type II glycogenosis.
    de Barsy T, Ferrière G, Fernandez-Alvarez E.
    Acta Neuropathol; 1979 Aug 14; 47(3):245-7. PubMed ID: 384741
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  • 10. [EMG-findings in typ-II-glycogenosis (Pompe's disease, acid maltase deficiency) (author's transl)].
    Gehlen W, Stefan H.
    EEG EMG Z Elektroenzephalogr Elektromyogr Verwandte Geb; 1978 Mar 14; 9(1):24-9. PubMed ID: 416945
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  • 17. Acid maltase deficiency: a case study and review of the pathophysiological changes and proposed therapeutic measures.
    Isaacs H, Savage N, Badenhorst M, Whistler T.
    J Neurol Neurosurg Psychiatry; 1986 Sep 14; 49(9):1011-8. PubMed ID: 3093639
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  • 18. Glycogen storage disease in skeletal muscle. Morphological, ultrastructural and biochemical aspects in 10 cases.
    Cabello A, Benlloch T, Franch O, Feliú JF, Ricoy JR.
    Acta Neuropathol Suppl; 1981 Sep 14; 7():297-300. PubMed ID: 6939256
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