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#	Item
981	[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
982	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
983	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
984	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
985	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
986	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
987	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
988	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
989	Microsoft Word - fig1_FINAL.doc Add to Reading List Source URL: amdapompe.ehclients.com Language: English - Date: 2011-01-02 22:46:24 Immune system Glycogen storage disease type II Hepatology Lysosomal storage disease Antibody Alglucosidase alfa Monoclonal antibodies Enzyme replacement therapy Medicine Health Biology
990	Login: Register Home Browse Add to Reading List Source URL: amdapompe.ehclients.com Language: English - Date: 2010-08-10 22:01:15 Inborn errors of carbohydrate metabolism Health Carbohydrates Rare diseases Mammalian target of rapamycin Signal transduction Glycogen storage disease type II Glycogen Sirolimus Biology Hepatology Medicine

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