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Chapter 37 - Pompe Disease

from Disorders of Infancy

Published online by Cambridge University Press:  28 April 2017

Juan M. Pascual
Juan M. Pascual
Affiliation:
University of Texas Southwestern Medical Center, Dallas
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Progressive Brain Disorders in Childhood , pp. 136 - 140
Publisher: Cambridge University Press
Print publication year: 2017

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References

Angelini, C. (2015). Spectrum of metabolic myopathies. Biochim Biophys Acta. 1852(4):615–21.Google ScholarPubMed
Boustany, R.M. (2013). Lysosomal storage diseases–the horizon expands. Nat Rev Neurol.; 9(10):583–98.Google Scholar
Pascual, J.M, Roe, C.R. (2013). Systemic metabolic abnormalities in adult-onset acid maltase deficiency: Beyond muscle glycogen accumulation. JAMA Neurol. 70(6):756–63.Google Scholar

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  • Pompe Disease
  • Juan M. Pascual, University of Texas Southwestern Medical Center, Dallas
  • Book: Progressive Brain Disorders in Childhood
  • Online publication: 28 April 2017
  • Chapter DOI: https://doi.org/10.1017/9781107323704.038
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  • Pompe Disease
  • Juan M. Pascual, University of Texas Southwestern Medical Center, Dallas
  • Book: Progressive Brain Disorders in Childhood
  • Online publication: 28 April 2017
  • Chapter DOI: https://doi.org/10.1017/9781107323704.038
Available formats
×

Save book to Google Drive

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Google Drive.

  • Pompe Disease
  • Juan M. Pascual, University of Texas Southwestern Medical Center, Dallas
  • Book: Progressive Brain Disorders in Childhood
  • Online publication: 28 April 2017
  • Chapter DOI: https://doi.org/10.1017/9781107323704.038
Available formats
×