Literature DB >> 7662715

McArdle's disease-muscle glycogen phosphorylase deficiency.

C Bartram1, R H Edwards, R J Beynon.   

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Year:  1995        PMID： 7662715     DOI： 10.1016/0925-4439(95)00060-h

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN： 0006-3002


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  4 in total

1.  Mutations in the liver glycogen phosphorylase gene (PYGL) underlying glycogenosis type VI.

Authors:  B Burwinkel; H D Bakker; E Herschkovitz; S W Moses; Y S Shin; M W Kilimann
Journal:  Am J Hum Genet       Date:  1998-04       Impact factor: 11.025

2.  Measurement of the turnover of glycogen phosphorylase by GC/MS using stable isotope derivatives of pyridoxine (vitamin B6).

Authors:  R J Beynon; D M Leyland; R P Evershed; R H Edwards; S P Coburn
Journal:  Biochem J       Date:  1996-07-15       Impact factor: 3.857

3.  McArdle's disease: A differential diagnosis of idiopathic toe walking.

Authors:  David Pomarino; Stephan Martin; Andrea Pomarino; Stefanie Morigeau; Saskia Biskup
Journal:  J Orthop       Date:  2018-05-08

4.  Higher oxidative stress in skeletal muscle of McArdle disease patients.

Authors:  Jan J Kaczor; Holly A Robertshaw; Mark A Tarnopolsky
Journal:  Mol Genet Metab Rep       Date:  2017-06-09
  4 in total

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