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Journal Abstract Search

561 related items for PubMed ID: 6304667

  • 1. Glycogen storage disease. Studies related to the mechanism of glycogenosome formation.
    Iwamasa T, Ninomiya N, Fukuda S, Hamada T, Hirashima M, Osame M.
    Pathol Res Pract; 1983 Mar; 176(2-4):236-52. PubMed ID: 6304667
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  • 2. [A study of the abnormal polysaccharide in a child with type IV glycogen storage disease (author's transl)].
    Scotto JM, de Barsy T, Hadchouel M, Bernard O.
    Arch Fr Pediatr; 1981 Dec; 38 Suppl 1():837-41. PubMed ID: 6949501
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  • 3. Prenatal diagnosis in glycogen storage diseases.
    Chen YT, Bali D, Sullivan J.
    Prenat Diagn; 2002 May; 22(5):357-9. PubMed ID: 12001186
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  • 4. Laboratory diagnosis of the neuromuscular glycogen storage diseases.
    Farmer PM.
    Ann Clin Lab Sci; 1982 May; 12(6):431-8. PubMed ID: 6817693
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  • 5. Severe course of glycogen storage disease type II (Pompe's disease) without development of cardiomegalia.
    Ullrich K, Gröbe H, Korinthenberg R, von Bassewitz DB.
    Pathol Res Pract; 1986 Oct; 181(5):627-32. PubMed ID: 2947052
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  • 6. Renal cortical tubular glycogen localization in glycogenosis type II (Pompe's disease).
    Witzleben CL.
    Lab Invest; 1969 May; 20(5):424-9. PubMed ID: 4305720
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  • 10. Glycogen storage disease diagnosed in adults.
    Pears JS, Jung RT, Hopwood D, Waddell ID, Burchell A.
    Q J Med; 1992 Mar; 82(299):207-22. PubMed ID: 1321455
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  • 12. [Cardiomuscular lysosomal glycogenosis in adults without known enzyme deficiency. A cause of familial myocardiopathy and lysosomal glycogen overload with normal acid maltase].
    Bru P, Pellissier JF, Gatau-Pelanchon J, Faugère G, de Barsy T, Levy S, Gérard R.
    Arch Mal Coeur Vaiss; 1988 Jan; 81(1):109-14. PubMed ID: 3130016
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  • 13. Vacuolar myopathy with type 2 A fiber atrophy and type 2 B fiber deficiency. A case of childhood form acid alpha-1,4-glucosidase deficiency.
    Matsuishi T, Terasawa K, Yoshida I, Yano E, Yamashita F, Hidaka T, Ishihara O, Yoshino M, Nonaka I, Kurokawa T, Nakamura Y.
    Neuropediatrics; 1982 Nov; 13(4):173-6. PubMed ID: 6818487
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  • 14. [Pompe's disease or glycogen storage disease].
    Vanto T, Salmi TT, Kalimo H, Lang H, Näntö V, Berlin M, Penttinen R.
    Duodecim; 1982 Nov; 98(9):709-16. PubMed ID: 7049663
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  • 15. Glycogen storage disease type II: enzymatic screening in dried blood spots on filter paper.
    Chamoles NA, Niizawa G, Blanco M, Gaggioli D, Casentini C.
    Clin Chim Acta; 2004 Sep; 347(1-2):97-102. PubMed ID: 15313146
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  • 16. Genetic aspects of muscle glycogenosis.
    Moses SW, Bashan N.
    Prog Clin Biol Res; 1989 Sep; 306():149-61. PubMed ID: 2500668
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  • 17. 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 Sep; 45(1):51-61. PubMed ID: 6199887
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