The clinical and electrodiagnostic characteristics of Pompe disease with post-enzyme replacement therapy findings
Author:
Publisher
Elsevier BV
Subject
Physiology (medical),Neurology (clinical),Neurology,Sensory Systems
Reference23 articles.
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4. Muscle MRI findings in siblings with juvenile-onset acid maltase deficiency (Pompe disease);Dlamini;Neuromuscul Disord,2008
5. Acid maltase deficiency in adults: studies in four cases of a syndrome which may mimic muscular dystrophy or other myopathies;Engel;Brain,1970
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