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Glycogen storage disease type II
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41	THE JOURNAL OF GENE MEDICINE RESEARCH ARTICLE J Gene Med 2010;12: 881–891. Published online 22 October 2010 in Wiley Online Library (wileyonlinelibrary.com) DOI: [removed]jgm[removed]Antibody formation and mannose-6-phosp Add to Reading List Source URL: amdapompe.ehclients.com Language: English - Date: 2011-06-06 01:04:00 Hepatology Gene delivery Applied genetics Inborn errors of carbohydrate metabolism Rare diseases Glycogen storage disease type II Adeno-associated virus Acid alpha-glucosidase Gene therapy Biology Medicine Health
42	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 Add to Reading List Source URL: amdapompe.ehclients.com Language: English - Date: 2011-05-07 19:52:59 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
43	Molecular Bases of Disease: Glycosylation-independent Lysosomal Targeting of Acid α-Glucosidase Enhances Muscle Glycogen Clearance in Pompe Mice John A. Maga, Jianghong Zhou, Ravi Kambampati, Susan Peng, Xu Wang, Richar Add to Reading List Source URL: amdapompe.ehclients.com Language: English - Date: 2013-07-21 20:12:27 Peptide hormones Hepatology Glycogen storage disease type II Mannose 6-phosphate Insulin-like growth factor 1 Insulin-like growth factor BioMarin Pharmaceutical Lysosomal storage disease Alpha-glucosidase Biology Cell biology Growth factors
44	Editorial For reprint orders, please contact [removed] Immune modulation in Pompe disease treated with enzyme replacement therapy Expert Rev. Clin. Immunol. 8(6), 497–[removed]) Add to Reading List Source URL: amdapompe.ehclients.com Language: English - Date: 2013-05-26 18:40:15 Anatomy Immune system Glycoproteins Glycogen storage disease type II Hepatology Rituximab Antibody Lysosomal storage disease Intravenous immunoglobulin Medicine Biology Immunology
45	Use of cardiac magnetic resonance imaging to evaluate cardiac structure, function and fibrosis in children with infantile Pompe disease on enzyme replacement therapy Add to Reading List Source URL: amdapompe.ehclients.com Language: English - Date: 2011-02-13 00:22:26 Cardiac imaging Rare diseases Cardiomyopathy Aging-associated diseases Medical emergencies Cardiac magnetic resonance imaging Glycogen storage disease type II Echocardiography Lysosomal storage disease Health Medicine Cardiology
46	[Autophagy 5:5, [removed]; 1 July 2009]; ©2009 Landes Bioscience Autophagic Punctum The values and limits of an in vitro model of Pompe disease The best laid schemes o’ mice an’ men…† Add to Reading List Source URL: amdapompe.ehclients.com Language: English - Date: 2010-07-21 22:33:29 Organelles Hepatology Muscular system Exercise physiology Cellular processes Autophagy Lysosome Glycogen storage disease type II Endosome Biology Anatomy Cell biology
47	United States Pompe Community Update, August 1, 2014 Genzyme is pleased to provide an update to the Pompe Community regarding the recent United States (U.S.) Food and Drug Administration’s (FDA) approval of an expande Add to Reading List Source URL: amdapompe.ehclients.com Language: English - Date: 2014-08-01 16:23:02 Hepatology Alglucosidase alfa Genzyme Anaphylaxis William Canfield Medicine Health Glycogen storage disease type II
48	SEARCH: Blood, 1 July 2010, Vol. 115, No. 26, pp[removed]Prepublished online as a Blood First Edition Paper on April 12, 2010; DOI[removed]blood[removed]. Advanced Add to Reading List Source URL: amdapompe.ehclients.com Language: English - Date: 2010-08-10 22:36:57 Glycogen storage disease type II Hepatology Gene therapy Hematopoietic stem cell Viral vector Haematopoiesis Biology Gene delivery Rare diseases
49	Severely impaired health status at diagnosis of Pompe disease: A cross-sectional analysis to explore the potential utility of neonatal screening Add to Reading List Source URL: amdapompe.ehclients.com Language: English - Date: 2013-05-26 18:23:02 Glycogen storage disease type II Lysosomal storage disease Alglucosidase alfa Amyotrophic lateral sclerosis Health Rare diseases Medicine
50	The FASEB Journal • Research Communication Adjunctive albuterol enhances the response to enzyme replacement therapy in late-onset Pompe disease Dwight D. Koeberl,,1 Stephanie Austin, Laura E. Case,† Edward C. Smit Add to Reading List Source URL: amdapompe.ehclients.com Language: English - Date: 2014-08-13 23:54:32 Rare diseases Glycogen storage disease type II Hepatology Lysosomal storage disease Acid alpha-glucosidase Salbutamol Enzyme replacement therapy Methadone Medicine Chemistry Health

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