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Glycogen
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241	Neuromuscular Disorders xxx[removed]xxx–xxx 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: 2011-01-02 22:37:30 Respiratory therapy Rare diseases Inborn errors of carbohydrate metabolism Glycogen storage disease type II Hepatology Lysosomal storage disease Physical therapy Alglucosidase alfa Spirometry Medicine Health Pulmonary function testing
242	Register or Login: Search This Periodical Password: Add to Reading List Source URL: amdapompe.ehclients.com Language: English - Date: 2010-08-10 22:42:20 Glycogen storage disease type II Hepatology Rotterdam Erasmus MC Geography of Europe Health Rare diseases Medicine
243	[removed]-0329 PEDIATRIC RESEARCH Copyright © 2009 International Pediatric Research Foundation, Inc. Vol. 66, No. 3, 2009 Printed in U.S.A. Add to Reading List Source URL: amdapompe.ehclients.com Language: English - Date: 2010-07-21 22:36:10 Anatomy Glycogen storage disease type II Hepatology Motor neurone disease Alglucosidase alfa Amyotrophic lateral sclerosis Heart failure Medicine Health Rare diseases
244	[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
245	Login: Register Home Browse Add to Reading List Source URL: amdapompe.ehclients.com Language: English - Date: 2010-08-10 22:47:20 Glycogen storage disease type II Hepatology Alglucosidase alfa Medical genetics Desensitization Molecular genetics Enzyme replacement therapy Medicine Health Lysosomal storage diseases
246	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
247	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: 2013-05-26 18:16:26 Glycogen storage disease type II Hepatology Orphan drugs Lysosomal storage disease Enzyme replacement therapy ERT Alglucosidase alfa End point of clinical trials Amyotrophic lateral sclerosis Health Medicine Rare diseases
248	Hindawi Publishing Corporation Case Reports in Medicine Volume 2009, Article ID[removed], 4 pages doi:[removed][removed]Case Report Add to Reading List Source URL: amdapompe.ehclients.com Language: English - Date: 2010-07-21 22:30:08 Medicine Glycogen storage disease type II Whole body vibration Strength training Muscle Physical strength Duchenne muscular dystrophy Creatine Galileo Exercise Health Anatomy
249	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
250	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

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