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Journal Abstract Search

200 related items for PubMed ID: 2957974

  • 1. Juvenile polysaccharidosis with cardioskeletal myopathy.
    Greene GM, Weldon DC, Ferrans VJ, Cheatham JP, McComb RD, Brown BI, Gumbiner CH, Vanderhoof JA, Itkin PG, McManus BM.
    Arch Pathol Lab Med; 1987 Oct; 111(10):977-82. PubMed ID: 2957974
    [Abstract] [Full Text] [Related]

  • 2. Type IV glycogen storage disease: first reported case in Thailand.
    Hemsrichart V, Karalak S, Thakerngpol K, Stitnimankarn T.
    J Med Assoc Thai; 1989 Dec; 72(12):697-700. PubMed ID: 2628538
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  • 3. An adult case of Andersen's disease--Type IV glycogenosis. A clinical, histochemical, ultrastructural and biochemical study.
    Ferguson IT, Mahon M, Cumming WJ.
    J Neurol Sci; 1983 Dec; 60(3):337-51. PubMed ID: 6579239
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  • 5. [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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  • 6. [Polysaccharide amylopectin-type storage myopathy].
    Calore EE, Pellissier JF, Figarella-Branger D, de Barsy T, Pouget J, Serratrice G.
    Rev Neurol (Paris); 1992 Dec; 148(11):696-703. PubMed ID: 1303560
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  • 7. [Differential diagnosis of glycogenoses].
    Rozenfel'd EL, Popova IA.
    Arkh Patol; 1980 Dec; 42(12):61-71. PubMed ID: 7011274
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  • 10. 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 Dec; 11(1):39-44. PubMed ID: 132627
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  • 11. A biochemical and ultrastructural study of liver, muscle, heart and kidney in type II glycogenosis.
    Bruni CB, Paluello FM.
    Virchows Arch B Cell Pathol; 1970 Dec; 4(3):196-207. PubMed ID: 4983073
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  • 12. Nervous system involvement in type IV glycogenosis.
    McMaster KR, Powers JM, Hennigar GR, Wohltmann HJ, Farr GH.
    Arch Pathol Lab Med; 1979 Mar; 103(3):105-11. PubMed ID: 284761
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  • 13. [Clinical and biochemical correlations in certain metabolic myopathies].
    de Barsy T.
    Bull Mem Acad R Med Belg; 1992 Mar; 147(10):385-92; discussion 392-3. PubMed ID: 1303789
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  • 14. [A vacuolar myopathy: autophagic glycogenosis of late onset. Ultrastructural study].
    Sengel A, Stoebner P, Isch F.
    Ann Anat Pathol (Paris); 1971 Mar; 16(1):47-54. PubMed ID: 5283285
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  • 16. Skin biopsy findings in glycogenosis III: clinical, biochemical, and electrophysiological correlations.
    Sancho S, Navarro C, Fernández JM, Domínguez C, Ortega A, Roig M, Cervera C.
    Ann Neurol; 1990 May; 27(5):480-6. PubMed ID: 2360788
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  • 17. Juvenile hereditary polyglucosan body disease with complete branching enzyme deficiency (type IV glycogenosis).
    Schröder JM, May R, Shin YS, Sigmund M, Nase-Hüppmeier S.
    Acta Neuropathol; 1993 May; 85(4):419-30. PubMed ID: 7683169
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  • 18. [A study of neuromuscular disorders in type III glycogenosis (Cori-Forbes disease)].
    Yamane K, Osawa M, Maruyama S, Haruta S, Sekiguchi M.
    Rinsho Shinkeigaku; 1984 May; 24(5):453-62. PubMed ID: 6592067
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