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Alpha-glucosidase
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11	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: www.nature.com Language: English - Date: 2012-01-04 14:12:58 Genetic genealogy Rare diseases Hepatology Genetics Glycogen storage disease type II Glycogen storage disease type V Lysosomal storage disease Genotype Acid alpha-glucosidase Health Inborn errors of carbohydrate metabolism Medicine
12	NDA[removed]S-008 Page 3 Glyset® miglitol tablets For Oral Use Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2009-05-13 14:25:20 Endocrinology Anti-diabetic medication Alpha-glucosidase inhibitor Diabetes management Hypoglycemia Miglitol Blood sugar Glycated hemoglobin Pioglitazone Diabetes Endocrine system Medicine
13	NIH Public Access Author Manuscript Am J Med Genet C Semin Med Genet. Author manuscript; available in PMC 2013 February 15. NIH-PA Author Manuscript Add to Reading List Source URL: amdapompe.ehclients.com Language: English - Date: 2014-03-02 20:04:03 Autophagy Programmed cell death Inborn errors of carbohydrate metabolism Rare diseases Hepatology Glycogen storage disease type II Acid alpha-glucosidase Lysosomal storage disease Lysosome Biology Cell biology Cellular processes
14	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
15	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
16	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
17	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
18	Wens et al. Orphanet Journal of Rare Diseases 2013, 8:182 http://www.ojrd.com/content[removed]RESEARCH Open Access Add to Reading List Source URL: amdapompe.ehclients.com Language: English - Date: 2014-02-22 17:45:50 Motor neurone disease Lysosomal storage diseases Glycogen storage disease type II Hepatology Acid alpha-glucosidase Amyotrophic lateral sclerosis Ptosis Health Rare diseases Medicine
19	Register or Login: Password: Search This Periodical Add to Reading List Source URL: amdapompe.ehclients.com Language: English - Date: 2010-08-10 22:40:31 Inborn errors of carbohydrate metabolism Enzymes Rare diseases Glycogen storage disease type II Alpha-glucosidase Maltase Erasmus MC Medical genetics Glycogen storage disease Medicine Health Hepatology
20	Hindawi Publishing Corporation Case Reports in Obstetrics and Gynecology Volume 2012, Article ID[removed], 4 pages doi:[removed][removed]Case Report Add to Reading List Source URL: amdapompe.ehclients.com Language: English - Date: 2013-05-26 18:31:57 Pregnancy Lysosomal storage diseases Rare diseases Inborn errors of carbohydrate metabolism Glycogen storage disease type II Acid alpha-glucosidase Enzyme replacement therapy Medical genetics Maternal-fetal medicine Medicine Health Obstetrics