Long-term enzyme-replacement therapy (ERT) with alglucosidase alfa: Evolution of two siblings with juvenile late-onset Pompe disease
Author:
Publisher
Elsevier BV
Subject
Clinical Neurology,Neurology
Reference10 articles.
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3. Pompe disease (glycogen storage disease type II) in Argentineans: clinical manifestations and identification of 9 novel mutations;Palmer;Neuromuscul. Disord.,2007
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1. Treatment Dilemma in Children with Late-Onset Pompe Disease;Genes;2023-01-30
2. Insight into the phenotype of infants with Pompe disease identified by newborn screening with the common c.-32-13T > G “late-onset” GAA variant;Molecular Genetics and Metabolism;2017-11
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