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Glycogen storage disease
Results: 221

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71	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
72	De-hospitalization of the pediatric day surgery by means of a freestanding surgery center: pilot study in the lazio region Add to Reading List Source URL: amdapompe.ehclients.com Language: English - Date: 2013-07-21 20:13:54 Glycogen storage disease type II Hepatology Oropharyngeal dysphagia Motor neurone disease Dysphagia Swallowing Esophageal cancer Enzyme replacement therapy Aspiration pneumonia Medicine Health Rare diseases
73	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
74	Lachmann and Schoser Orphanet Journal of Rare Diseases 2013, 8:160 http://www.ojrd.com/content[removed]REVIEW Open Access Add to Reading List Source URL: amdapompe.ehclients.com Language: English - Date: 2014-02-22 17:47:38 Respiratory therapy Pulmonary function testing Respiratory physiology Clinical research Glycogen storage disease type II Lysosomal storage disease Spirometry Idiopathic pulmonary fibrosis Duchenne muscular dystrophy Medicine Health Pulmonology
75	Evidence for decline in the incidence of cystic fibrosis: a 35-year observational study in Brittany, France Add to Reading List Source URL: amdapompe.ehclients.com Language: English - Date: 2013-07-21 20:16:24 Muscular system Biopsy Rare diseases Inborn errors of carbohydrate metabolism Glycogen storage disease type II Hepatology Enzyme replacement therapy Muscle Autophagy Medicine Anatomy Biology
76 $Osteopathies / Traumatology / Glycogen storage disease type II / Hepatology / Osteoporosis / Lysosomal storage disease / Alendronic acid / Pathologic fracture / Bone density / Medicine / Health / Bone fractures$	Pediatr Radiol[removed]:437–445 DOI[removed]s00247[removed]y ORIGINAL ARTICLE Fractures in children with Pompe disease: a potential Add to Reading List Source URL: amdapompe.ehclients.com Language: English - Date: 2011-01-02 22:44:44 Osteopathies Traumatology Glycogen storage disease type II Hepatology Osteoporosis Lysosomal storage disease Alendronic acid Pathologic fracture Bone density Medicine Health Bone fractures
77	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
78	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
79	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
80	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

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