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Journal Abstract Search


126 related items for PubMed ID: 267557

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  • 6. [A retrospective study of six patients with late-onset Pompe disease].
    Saux A, Laforet P, Pagès AM, Figarella-Branger D, Pellissier JF, Pagès M, Labauge P.
    Rev Neurol (Paris); 2008 Apr; 164(4):336-42. PubMed ID: 18439925
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  • 11. 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; 26(13):1914-5. PubMed ID: 7002367
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  • 12. [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; 15(12):705-8. PubMed ID: 342670
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  • 13. Pompe's disease: ultrastructural alterations of muscle tissue in parents.
    Pellegrini G, Mosca G, Cerri C.
    Acta Neurol Scand; 1978 Mar; 57(3):216-22. PubMed ID: 276244
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  • 15. [Adult form of acid maltase deficiency presenting as progressive spinal muscular atrophy].
    Pongratz D, Kötzner H, Hübner G, Deufel T, Wieland OH.
    Dtsch Med Wochenschr; 1984 Apr 06; 109(14):537-41. PubMed ID: 6368168
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  • 16. Childhood acid maltase deficiency. A clinical, biochemical, and morphologic study of three patients.
    Matsuishi T, Yoshino M, Terasawa K, Nonaka I.
    Arch Neurol; 1984 Jan 06; 41(1):47-52. PubMed ID: 6360103
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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 06; 49(9):1011-8. PubMed ID: 3093639
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  • 20. Acid maltase deficiency in adults: studies in four cases of a syndrome which may mimic muscular dystrophy or other myopathies.
    Engel AG.
    Brain; 1970 Sep 06; 93(3):599-616. PubMed ID: 4918728
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