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Journal Abstract Search

154 related items for PubMed ID: 4522354

  • 21. New kind of cytoplasmic inclusions of plasma cells in acid maltase deficiency.
    Pralle H, Schröder R, Löffler H.
    Acta Haematol; 1975; 53(2):109-17. PubMed ID: 164754
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  • 26. Adult acid maltase deficiency. Abnormalities in fibroblasts cultured from patients.
    Angelini C, Engel AG, Titus JL.
    N Engl J Med; 1972 Nov 09; 287(19):948-51. PubMed ID: 4507329
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  • 27. [A vacuolar myopathy: autophagic glycogenosis of late onset. Ultrastructural study].
    Sengel A, Stoebner P, Isch F.
    Ann Anat Pathol (Paris); 1971 Nov 09; 16(1):47-54. PubMed ID: 5283285
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  • 28. Generalized glycogenosis type II (Pompe's disease).
    Nihill MR, Wilson DS, Hugh-Jones K.
    Arch Dis Child; 1970 Feb 09; 45(239):122-9. PubMed ID: 4245388
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  • 29. [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 09; 9(1):24-9. PubMed ID: 416945
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  • 30. [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 Mar 09; 16(1):85-92. PubMed ID: 4327013
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  • 31. Electron microscopy of ocular muscle in type II glycogenosis (Pompe's disease).
    Smith RS, Reinecke RD.
    Am J Ophthalmol; 1972 Jun 09; 73(6):965-70. PubMed ID: 4260696
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  • 32. Pompe's disease: ultrastructural alterations of muscle tissue in parents.
    Pellegrini G, Mosca G, Cerri C.
    Acta Neurol Scand; 1978 Mar 09; 57(3):216-22. PubMed ID: 276244
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  • 33. Pompe's disease. Electromyographic, electron microscopic, and cardiovascular aspects.
    Bordiuk JM, Legato MJ, Lovelace RE, Blumenthal S.
    Arch Neurol; 1970 Aug 09; 23(2):113-9. PubMed ID: 4246920
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  • 34. [Biochemical diagnosis of glycogenosis type II (acid maltase deficiency) (author's transl)].
    Pilz H, Goebel HH, Stefan H, Seidel D, Kohlschütter A.
    J Clin Chem Clin Biochem; 1977 Dec 09; 15(12):705-8. PubMed ID: 342670
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  • 35. 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 09; 4(3):196-207. PubMed ID: 4983073
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  • 36. [Histochemical study of muscular basophil substances in Pompe's disease].
    Palladini G, Martin JJ.
    Acta Neurol (Napoli); 1972 Dec 09; 27(2):140-2. PubMed ID: 4261280
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  • 37. Apparent normal leukocyte acid maltase activity in glycogen storage disease type II (Pompe's disease).
    Potter JL, Robinson HB, Kramer JD, Schafter IA.
    Clin Chem; 1980 Dec 09; 26(13):1914-5. PubMed ID: 7002367
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  • 38. Renal cortical tubular glycogen localization in glycogenosis type II (Pompe's disease).
    Witzleben CL.
    Lab Invest; 1969 May 09; 20(5):424-9. PubMed ID: 4305720
    [No Abstract] [Full Text] [Related]

  • 39. Late infantile acid maltase deficiency.
    Swaiman KF, Kennedy WR, Sauls HS.
    Arch Neurol; 1968 Jun 09; 18(6):642-8. PubMed ID: 5240358
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  • 40. Increased excretion of a glucose-containing tetrasaccharide in the urine of a patient with glycogen storage disease type II (Pompe's disease).
    Hallgren P, Hansson G, Henriksson KG, Häger A, Lundblad A, Svensson S.
    Eur J Clin Invest; 1974 Dec 05; 4(6):429-33. PubMed ID: 4531383
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