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Alpha-glucosidase
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21	NIH Public Access Author Manuscript Curr Gene Ther. Author manuscript; available in PMC 2010 June 29. NIH-PA Author Manuscript Add to Reading List Source URL: amdapompe.ehclients.com Language: English - Date: 2010-07-21 22:27:42 Applied genetics Biotechnology Immune system Glycogen storage disease type II Acid alpha-glucosidase Adeno-associated virus Gene therapy CD25 Lysosomal storage disease Biology Medicine Immunology
22	NIH Public Access Author Manuscript Mol Genet Metab. Author manuscript; available in PMC 2009 May 11. NIH-PA Author Manuscript Add to Reading List Source URL: amdapompe.ehclients.com Language: English - Date: 2010-07-21 22:46:18 Rare diseases Lysosomal storage diseases Acid alpha-glucosidase Glycogen storage disease type II Autophagy Lysosome Myosatellite cell Skeletal striated muscle Glycogen Biology Cell biology Hepatology
23	[Autophagy 3:6, [removed]; November/December 2007]; ©2007 Landes Bioscience Research Paper ©2007 LANDES BIOSCIENCE.BiDO NOT DISTRIBUTE. Add to Reading List Source URL: amdapompe.ehclients.com Language: English - Date: 2010-08-10 22:44:52 Cellular processes Autophagy Programmed cell death Rare diseases Inborn errors of carbohydrate metabolism Glycogen storage disease type II Lysosomal storage disease Lysosome Acid alpha-glucosidase Biology Anatomy Muscular system
24	Neuromuscular Disorders[removed]–774 Contents lists available at ScienceDirect Neuromuscular Disorders journal homepage: www.elsevier.com/locate/nmd Add to Reading List Source URL: amdapompe.ehclients.com Language: English - Date: 2011-05-07 19:58:15 Lysosomal storage diseases Glycogen storage disease type II Hepatology Motor neurone disease Alglucosidase alfa Alpha-glucosidase Placebo Amyotrophic lateral sclerosis Health Medicine Rare diseases
25	Contact: Investors: Traci McCarty BioMarin Pharmaceutical Inc[removed] Add to Reading List Source URL: amdapompe.ehclients.com Language: English - Date: 2014-06-08 18:46:42 Genetic genealogy BioMarin Pharmaceutical Glycogen storage disease type II Acid alpha-glucosidase Lysosomal storage disease Mucopolysaccharidosis Alglucosidase alfa Neuronal ceroid lipofuscinosis Tetrahydrobiopterin Health Rare diseases Medicine
26	ARTICLE The angiotensin-converting enzyme insertion/deletion polymorphism modifies the clinical outcome in patients with Pompe disease Paola de Filippi, PhD1, Sabrina Ravaglia, MD, PhD2, Bruno Bembi, MD3, Alfredo Costa, Add to Reading List Source URL: amdapompe.ehclients.com Language: English - Date: 2010-04-02 02:44:57 Rare diseases Genetic genealogy Hepatology Genetics Glycogen storage disease type II Glycogen storage disease type V Lysosomal storage disease Acid alpha-glucosidase Duchenne muscular dystrophy Health Inborn errors of carbohydrate metabolism Medicine
27	J Inherit Metab Dis DOI[removed]s10545[removed]ORIGINAL ARTICLE Facial-muscle weakness, speech disorders and dysphagia Add to Reading List Source URL: amdapompe.ehclients.com Language: English - Date: 2012-01-17 11:57:59 Motor neurone disease Glycogen storage disease type II Hepatology Lysosomal storage disease Dysphagia Swallowing Acid alpha-glucosidase Amyotrophic lateral sclerosis Hypotonia Health Medicine Rare diseases
28	ARTICLE IN PRESS Available online at www.sciencedirect.com Neuromuscular Disorders xxx[removed]xxx–xxx www.elsevier.com/locate/nmd Add to Reading List Source URL: amdapompe.ehclients.com Language: English - Date: 2013-08-24 22:47:13 Knowledge Glycogen storage disease type II Rasch model Item response theory Patient-reported outcome Scale Acid alpha-glucosidase Rasch Level of measurement Psychometrics Statistics Education
29	Pain in adult patients with Pompe disease Add to Reading List Source URL: amdapompe.ehclients.com Language: English - Date: 2013-08-24 22:34:38 Rare diseases Nociception Glycogen storage disease type II Hepatology Acid alpha-glucosidase Fabry disease Lysosomal storage disease Chronic pain Medicine Health Pain
30	NIH Public Access Author Manuscript Neurotherapeutics. Author manuscript; available in PMC 2009 October 14. NIH-PA Author Manuscript Add to Reading List Source URL: amdapompe.ehclients.com Language: English - Date: 2010-07-21 23:05:58 Inborn errors of carbohydrate metabolism Rare diseases Glycogen storage disease type II Lysosomal storage disease Acid alpha-glucosidase Enzyme replacement therapy Glycogen Medicine Health Hepatology