Glycogen - PDFSEARCH.IO - Document Search Engine

Glycogen
Results: 481

#	Item
271	Orphanet Journal of Rare Diseases This Provisional PDF corresponds to the article as it appeared upon acceptance. Fully formatted PDF and full text (HTML) versions will be made available soon. Survival and associated fa Add to Reading List Source URL: amdapompe.ehclients.com Language: English - Date: 2011-06-05 21:33:58 Hepatology Glycogen storage disease type II Medical terms Lysosomal storage disease Five-year survival rate Amyotrophic lateral sclerosis Health Medicine Rare diseases
272	"DUB.ZPMPHJDBt999Q EDITORIAL Early is better? A new algorithm for early diagnosis Add to Reading List Source URL: amdapompe.ehclients.com Language: English - Date: 2014-02-22 17:32:25** Lysosomal storage diseases Inborn errors of carbohydrate metabolism Glycogen storage disease type II Hepatology Acid alpha-glucosidase Limb-girdle muscular dystrophy Muscular dystrophy Amyotrophic lateral sclerosis Health Rare diseases Medicine
273	NIH Public Access Author Manuscript Gene Ther. Author manuscript; available in PMC 2011 June 1. NIH-PA Author Manuscript Add to Reading List Source URL: amdapompe.ehclients.com Language: English - Date: 2011-06-05 23:35:12 Hepatology Gene delivery Applied genetics Muscular system Exercise physiology Glycogen storage disease type II Acid alpha-glucosidase Adeno-associated virus Skeletal striated muscle Biology Anatomy Medicine
274	RESEARCH ARTICLE A Large-Scale Nationwide Newborn Screening Program for Pompe Disease in Taiwan: Towards Effective Diagnosis and Treatment Chia-Feng Yang,1 Hao-Chuan Liu,1 Ting-Rong Hsu,1,2 Fang-Chih Tsai,1 Sheng-Fong C Add to Reading List Source URL: amdapompe.ehclients.com Language: English - Date: 2014-02-22 17:37:46 Chemical pathology Inborn errors of carbohydrate metabolism Glycogen storage disease type II Hepatology Lysosomal storage disease Acid alpha-glucosidase Hypotonia Alglucosidase alfa Lactate dehydrogenase Medicine Health Rare diseases
275	Glycoengineered Acid α-Glucosidase With Improved Efficacy at Correcting the Metabolic Aberrations and Motor Function Deficits in a Mouse Model of Pompe Disease Add to Reading List Source URL: amdapompe.ehclients.com Language: English - Date: 2010-08-10 23:04:01 Hepatology Inborn errors of carbohydrate metabolism Enzymes Exercise physiology Muscular system Glycogen storage disease type II Acid alpha-glucosidase Glycogen Muscle Biology Anatomy Medicine
276	Intrapleural Administration of AAV9 Improves Neural and Cardiorespiratory Function in Pompe Disease Add to Reading List Source URL: amdapompe.ehclients.com Language: English - Date: 2013-07-21 20:08:21 Gene delivery Applied genetics Rare diseases Glycogen storage disease type II Hepatology Acid alpha-glucosidase Lysosomal storage disease Adeno-associated virus Gene therapy Medicine Biology Health
277	Enhanced efficacy of enzyme replacement therapy in Pompe disease through mannose-6-phosphate receptor expression in skeletal muscle Add to Reading List Source URL: amdapompe.ehclients.com Language: English - Date: 2011-05-07 19:47:12 Hepatology Inborn errors of carbohydrate metabolism Exercise physiology Muscular system Growth factors Glycogen storage disease type II Acid alpha-glucosidase Lysosomal storage disease Enzyme replacement therapy Biology Anatomy Medicine
278	amda AMDA Conference Call Transcript Session No. 4: Speaker: Add to Reading List Source URL: amdapompe.ehclients.com Language: English - Date: 2010-01-01 11:24:01 Hepatology Rare diseases Exercise physiology Neurological disorders Inborn errors of carbohydrate metabolism Glycogen storage disease type II Glycogen Muscle Virus Biology Medicine Health
279	original article © The American Society of Gene & Cell Therapy Spinal Delivery of AAV Vector Restores Enzyme Activity and Increases Ventilation in Pompe Mice Add to Reading List Source URL: amdapompe.ehclients.com Language: English - Date: 2012-01-17 11:40:39 Rare diseases Applied genetics Biotechnology Lysosomal storage diseases Motor neurone disease Glycogen storage disease type II Acid alpha-glucosidase Adeno-associated virus Amyotrophic lateral sclerosis Biology Health Medicine
280	LYSOSOMAL STORAGE DISORDER Quarterly Report PROFICIENCY TESTING August 2014 Add to Reading List Source URL: www.cdc.gov Language: English - Date: 2014-08-22 13:07:16 Krabbe disease Lysosomal storage disease Glycogen storage disease type II Galactosylceramidase Newborn screening Association of Public Health Laboratories Acid alpha-glucosidase Centers for Disease Control and Prevention Health Rare diseases Medicine

UPDATE