Diagnostic criteria for late-onset (childhood and adult) pompe disease-Reference-Cited by-同舟云学术

Diagnostic criteria for late-onset (childhood and adult) pompe disease

Published:2009-06-16 Issue:1 Volume:40 Page:149-160
ISSN:0148-639X
Container-title:Muscle & Nerve
language:en
Short-container-title:Muscle Nerve

Author:

Publisher

Wiley

Subject

Physiology (medical),Cellular and Molecular Neuroscience,Clinical Neurology,Physiology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/mus.21393/fullpdf

Reference62 articles.

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2. Glycogen storage disease types I and II: treatment updates;Koeberl;J Inherit Metab Dis,2007

3. Acid α-glucosidase deficiency (glycogenosis type II, Pompe disease);Raben;Curr Mol Med,2002

4. Pompe disease in infants and children;Kishnani;J Pediatr,2004

5. Pompe disease diagnosis and management guideline;Kishnani;Genet Med,2006

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