Skip to main content
SpringerLink
Log in

Phosphorylase kinase deficiency: Severe glycogen storage disease with evidence of autosomal recessive mode of inheritance

  • Letters to the Editors
  • Published:
European Journal of Pediatrics Aims and scope Submit manuscript

This is a preview of subscription content, log in via an institution to check access.

Access this article

Log in via an institution

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Institutional subscriptions

References

  • Bashan N, Iancu TC, Lerner A, Fraset D, Potashnik R, Moses SW (1981) Glycogenosis due to liver and muscle phosphorylase kinase deficiency Pediatr Res 15:299–303

    PubMed  Google Scholar 

  • Lederer B, van Hoof F, van den Berghe, Hers HG (1975) Glycogen phosphorylase and its converter enzymes in haemolysates of normal subjects and patients with type VI glycogen-storage disease. Biochem J 147: 23–35

    PubMed  Google Scholar 

  • Lederer B, van de Werne G, deBarsy Th, Hers HG (1980) The autosomal form of phosphorylase kinase deficiency in man: Reduced activity of the muscle enzyme. Biochem Biophys Res Commun 92:169–174

    PubMed  Google Scholar 

  • Mahler RF (1976) Disorders of glycogen metabolism. Clin Endocrinol Metab 5: 579–598

    PubMed  Google Scholar 

Download references

Author information

Authors and Affiliations

  1. Department of Pediatrics, University of Bergen, 5016 Haukeland Hospital, Bergen, Norway

    O. Søvik

  2. Department of Pathology, University of Bergen, 5016 Haukeland Hospital, Bergen, Norway

    B. Maehle

  3. Laboratoire de Chimie Physiologique, Université Catholique de Louvain, Brussels, Belgium

    Th. de Barsy

Authors
  1. O. Søvik
    View author publications

    You can also search for this author in PubMed Google Scholar

  2. Th. de Barsy
    View author publications

    You can also search for this author in PubMed Google Scholar

  3. B. Maehle
    View author publications

    You can also search for this author in PubMed Google Scholar

Rights and permissions

Reprints and permissions

About this article

Cite this article

Søvik, O., de Barsy, T. & Maehle, B. Phosphorylase kinase deficiency: Severe glycogen storage disease with evidence of autosomal recessive mode of inheritance. Eur J Pediatr 139, 210 (1982). https://doi.org/10.1007/BF01377363

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF01377363

Keywords

Search

Navigation