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Immunohistochemical demonstration of acid α-glucosidase in muscle in Pompe's disease

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References

  • Angelini, C. &Engel, A. G. (1972) Comparative study of acid maltase deficiency. Biochemical differences between infantile, childhood and adult types.Archs. Neurol. 26, 344–9.

    Google Scholar 

  • Baudhuin, P., Hers, H. G. &Loeb, H. (1964) An electron microscopic and biochemical study of type II glycogenosis.Lab. Invest. 13, 1139–52.

    PubMed  Google Scholar 

  • Beratis, N. G., Labadie, G. U. &Hirschhorn, K. (1978) Characterization of the molecular defect in infantile and adult acid α-glucosidase deficiency fibroblasts.J. clin. Invest. 62, 1264–74.

    PubMed  Google Scholar 

  • Bruni, C. B., Auricchio, F. &Covelli, I. (1963) Acid α-d-glucoside glycohydrolase from cattle liver. Isolation and properties.J. biol. Chem. 244, 4735–42.

    Google Scholar 

  • Debarsy, T., Jacquemin, P., Devos, P. &Hers, H. G. (1972) Rodent and human acid α-glucosidase. Purification, properties and inhibition by antibodies. Investigation in type II glycogenosis.Eur. J. Biochem. 31, 156–65.

    Article  PubMed  Google Scholar 

  • Garancis, J. C. (1968) Type II glycogenosis; biochemical and electron microscopic study.Am. J. Med. 44, 289–300.

    Article  PubMed  Google Scholar 

  • Hers, H. G. (1963) α-Glucosidase deficiency in generalized glycogen storage disease (Pompe's disease)Biochem. J. 86, 11–6.

    PubMed  Google Scholar 

  • Hug, G., Garancis, J. C., Schubert, W. K. &Kaplan, S. (1966) Glycogen storage disease type II, III, VII and IX; a biochemical and electron microscopic analysis.Am. J. Dis. Child. 111, 457–73.

    Google Scholar 

  • Iwamasa, T., Fukuda, S., Hamada, T. &Ninomiya, N. (1982a) Purification and immunohistochemistry of fetal acid α-glucosidase.Acta histochem. cytochem. 15, 198–207.

    Google Scholar 

  • Iwamasa, T., Ninomiya, N., Hamada, T. &Fukuda, S. (1982b) Immunohistochemical localization of acid α-glucosidase in rat liver.J. Histochem. Cytochem. 30, 378–89.

    PubMed  Google Scholar 

  • Koster, J. F., Slee, R. G., Van Der Klei-Van Moorsel, J. M., Rietra, P. J. G. M. &Lucas, C. J. (1976) Physico-chemical and immunochemical properties of acid α-glucosidase from various human tissue in relation to glycogenosis type II (Pompe's disease).Clin. Chim. Acta 68, 49–58.

    Article  PubMed  Google Scholar 

  • Koster, J. F. &Slee, R. G. (1977) Some properties of human liver acid α-glucosidase.Biochem. Biophy. Acta 482, 89–97.

    Google Scholar 

  • Murray, A. K., Brown, B. I. &Brown, D. H. (1978) The molecular hetrogenity of purified human liver lysosomal α-glucosidase (acid α-glucosidase).Archs Biochem. Biophys. 185, 511–29.

    Article  Google Scholar 

  • Nakagawa, M., Nakazato, O., Osame, M., Nakashima, H. &Igata, A. (1982) Muscle type acid maltase deficiency. An intermediate case between childhood type and adult type.Clin. Neurol. 22, 54–65.

    Google Scholar 

  • Sternberger, L. A., Hardy, P. H., Cuculis, J. J. &Meyer, H. G. (1970) The unlabeled antibody enzyme method of immunohistochemistry. Preparation and properties of soluble antigen-antibody complex (horseradish peroxidase-anti-horseradish peroxidase) and its use in indentification of spirochetes.J. Histochem. Cytochem. 18, 315–33.

    PubMed  Google Scholar 

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Authors and Affiliations

  1. Department of Pediatrics, Kumamoto University Medical School, Honjo, 860, Kumamoto, Japan

    Nobuyuki Ninomiya & Ichiro Matsuda

  2. Department of Pathology, Kumamoto University Medical School, Honjo, 860, Kumamoto, Japan

    Seiji Fukuda & Teruo Iwamasa

  3. Department of Internal Medicine, Kagoshima University Medical School, Ushukimachi, 890, Kagoshima, Japan

    Mitsuhiro Osame

Authors
  1. Nobuyuki Ninomiya
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  2. Ichiro Matsuda
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  3. Seiji Fukuda
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  4. Teruo Iwamasa
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  5. Mitsuhiro Osame
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Ninomiya, N., Matsuda, I., Fukuda, S. et al. Immunohistochemical demonstration of acid α-glucosidase in muscle in Pompe's disease. Histochem J 15, 601–604 (1983). https://doi.org/10.1007/BF01954150

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  • DOI: https://doi.org/10.1007/BF01954150

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