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Journal Abstract Search

163 related items for PubMed ID: 416945

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  • 2. [Glycogen storage disease (Pompe's disease) presenting as myopathy in the adult (author's transl)].
    Stefan H, Böker DK, Müller J, Gullotta F.
    Dtsch Med Wochenschr; 1977 Oct 21; 102(42):1512-4. PubMed ID: 269788
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  • 5. [Pseudodystrophic muscle glycogenosis in adults. (Acid maltase deficiency syndrome) (author's transl)].
    Gullotta F, Stefan H, Mattern H.
    J Neurol; 1976 Oct 21; 213(3):199-216. PubMed ID: 61260
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  • 12. [Prenatal diagnosis of glycogenosis II.--Pompe's disease].
    Macek M, Tomásová H, Hug G, Reinsteinová H, Seemanová E, Salichová J.
    Cesk Pediatr; 1977 Jul 21; 32(7):427-30. PubMed ID: 270392
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  • 13. Acid maltase deficiency in childhood. Early diagnosis and clinical follow-up of late-onset glycogen storage disease type II.
    di Fiore MT, Manfredi R, Marri L, Zucchini A, Azzaroli L, Manfredi G.
    Acta Neurol (Napoli); 1993 Aug 21; 15(4):258-67. PubMed ID: 8249669
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  • 15. [Laboratory diagnosis of lysosomal storage disease (glycoproteinosis Pompe's disease and Gaucher disease)].
    Shi HP, Zhang GX, Guo YF, Fang BL, Zhang WM, Chen F, Luo HY.
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 1985 Dec 21; 7(6):475-7. PubMed ID: 2940012
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  • 19. [Tests for the detection of inborn errors of metabolism--urinary alpha-glucosidase analysis for the detection of glycogen storage disease type II (author's transl)].
    Soyama K, Ono E.
    Rinsho Byori; 1978 Dec 21; 26(12):1022-6. PubMed ID: 370427
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