Literature DB >> 13088189

Studies in disorders of muscle. IX. Glycogen storage disease primarily affecting skeletal muscle and clinically resembling amyotonia congenita.

W KRIVIT, W J POLGLASE, F D GUNN, F H TYLER.   

Abstract

Entities:  

Keywords:  AMYOTONIA CONGENITA; GLYCOGEN/metabolism; MUSCLES/diseases

Mesh:

Substances:

Year:  1953        PMID: 13088189

Source DB:  PubMed          Journal:  Pediatrics        ISSN: 0031-4005            Impact factor:   7.124


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  6 in total

1.  The clinical course of glycogen disease.

Authors: 
Journal:  Can Med Assoc J       Date:  1963-01-05       Impact factor: 8.262

2.  [Neuromuscular form of glycogen storage disease].

Authors:  R SCHNABEL
Journal:  Virchows Arch Pathol Anat Physiol Klin Med       Date:  1958

3.  The amyotonia congenita syndrome.

Authors:  J N WALTON
Journal:  Proc R Soc Med       Date:  1957-05

4.  A MYOPATHY PRESENTING IN ADULT LIFE WITH FEATURES SUGGESTIVE OF GLYCOGEN STORAGE DISEASE.

Authors:  J M Holmes; C R Houghton; A L Woolf
Journal:  J Neurol Neurosurg Psychiatry       Date:  1960-11       Impact factor: 10.154

5.  Pompe's disease: an inborn lysosomal disorder with storage of glycogen. A study of brain and striated muscle.

Authors:  J J Martin; T de Barsy; F van Hoof; G Palladini
Journal:  Acta Neuropathol       Date:  1973-02-19       Impact factor: 17.088

6.  The liver in generalized glycogen storage disease. Light microscopic observations.

Authors:  A J McAdams; H E Wilson
Journal:  Am J Pathol       Date:  1966-07       Impact factor: 4.307

  6 in total

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