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Alpha acid
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#	Item
231	original article © The American Society of Gene Therapy Correction of Multiple Striated Muscles in Murine Pompe Disease Through Adeno-associated Add to Reading List Source URL: amdapompe.ehclients.com Language: English - Date: 2011-06-05 23:27:31 Applied genetics Hepatology Muscular system Adeno-associated virus Viral vector Glycogen storage disease type II Acid alpha-glucosidase Gene therapy Skeletal striated muscle Biology Gene delivery Molecular biology
232	Flexing to Aging: A Childrens Hospital Responds to a Maturing Workforce Add to Reading List Source URL: amdapompe.ehclients.com Language: English - Date: 2013-07-21 20:05:48 Orphan drugs Rare diseases Glycogen storage disease type II Hepatology Sirolimus Rituximab Acid alpha-glucosidase Enzyme replacement therapy Alglucosidase alfa Medicine Health Biology
233	"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
234	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
235	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
236	Ask the Expert Vilma Gabbay, M.D. Vilma Gabbay, M.D. is Medical Director of the Anita Saltz Institute for Anxiety and Mood Disorders and is Assistant Professor of Child and Adolescent Psychiatry at the NYU School of Med Add to Reading List Source URL: www.tsa-usa.org Language: English - Date: 2011-08-03 15:44:27 Medicine Omega-3 fatty acid Docosahexaenoic acid Fish oil Polyunsaturated fat Eicosapentaenoic acid Oily fish Alpha-Linolenic acid Ethyl eicosapentaenoic acid Fatty acids Nutrition Chemistry
237	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
238	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
239	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
240	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

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