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Rare diseases / Lysosomal storage diseases / Lipid storage disorders / Inborn errors of carbohydrate metabolism / Glycogen storage disease type II / Hepatology / Autophagy / Acid alpha-glucosidase / Enzyme replacement therapy / Biology / Health / Anatomy


Journal List > NIHPA Author Manuscripts Mol Genet Metab. Author manuscript; available in PMC 2010 December 1. Published in final edited form as: Mol Genet Metab[removed]December; 101(4): 324–331. Published online 2010 Au
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Document Date: 2011-05-07 19:52:59

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Burlingame / Eugene / Taipei / New York / Framingham / San Diego / St. Louis / Florence / /

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FDA Phase / Person Communication and Meetings / /

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National Institute of Arthritis / B. Bar / Virchows Arch / National Taiwan University Hospital / University School / /

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oil immersion objective / 2PEF imaging / imaging / harmonic imaging / energy / therapy for infantile glycogen storage disease / therapy for pompe disease / light chain / web version / /

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fatal cardiomyopathy / hypertrophic cardiomyopathy / Infantile acid maltase deficiency / JE / lysosomal storage disorders / Myopathy / skeletal muscle myopathy / Raben N. Dysfunction / Arthritis / rare autosomal recessive metabolic myopathy / muscle weakness / slowly progressive muscle weakness / starvation / Glycogen storage disease / disorder / lysosomal storage disease / MS / inflammatory diseases / pompe disease / lysosomal storage disorder / disease / infantile glycogen storage disease / late-onset glycogen storage disease type / Inherited Disease / common glycogen storage disorder / partial enzyme deficiency / Acid Maltase Deficiency / lysosomal storage diseases / respiratory insufficiency / neurodegenerative diseases / deficiency / Skin Diseases / /

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enzyme replacement therapy / /

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National Institute of Health / National Taiwan University School of Medicine / National Taiwan University Hospital / Pompe / office of Science & Technology / National Institute of Arthritis and Musculoskeletal / /

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