Glycogen - PDFSEARCH.IO - Document Search Engine

Glycogen
Results: 481

#	Item
261	J Inherit Metab Dis[removed]:597–602 DOI[removed]s10545[removed]ORIGINAL ARTICLE Hearing loss in Pompe disease revisited: results from a study Add to Reading List Source URL: amdapompe.ehclients.com Language: English - Date: 2011-08-06 17:40:55 Deafness Audiology Glycogen storage disease type II Hepatology Auditory brainstem response Sensorineural hearing loss Lysosomal storage disease Enzyme replacement therapy Hearing impairment Health Medicine Otology
262	NIH Public Access Author Manuscript Neurotherapeutics. Author manuscript; available in PMC 2009 October 14. NIH-PA Author Manuscript Add to Reading List Source URL: amdapompe.ehclients.com Language: English - Date: 2010-07-21 23:05:58 Inborn errors of carbohydrate metabolism Rare diseases Glycogen storage disease type II Lysosomal storage disease Acid alpha-glucosidase Enzyme replacement therapy Glycogen Medicine Health Hepatology
263	Letter to the Editor Eur Neurol 2012;68:75–78 DOI: [removed] Received: January 2, 2012 Accepted: April 2, 2012 Add to Reading List Source URL: amdapompe.ehclients.com Language: English - Date: 2013-05-26 18:43:36 Urinary incontinence Fecal incontinence Glycogen storage disease type II Pelvic floor Percutaneous tibial nerve stimulation Health Medicine Anatomy
264	Immunomodulatory Gene Therapy Prevents Antibody Formation and Lethal Hypersensitivity Reactions in Murine Pompe Disease Add to Reading List Source URL: amdapompe.ehclients.com Language: English - Date: 2011-06-05 23:30:36 Immune system Immunology Glycoproteins Applied genetics Biotechnology Adeno-associated virus Glycogen storage disease type II Acid alpha-glucosidase Gene therapy Biology Medicine Health
265	Enzyme replacement therapy and fatigue in adults with Pompe disease Add to Reading List Source URL: amdapompe.ehclients.com Language: English - Date: 2013-08-24 22:32:07 Neurological disorders Glycogen storage disease type II Hepatology Cancer-related fatigue Lysosomal storage disease Fatigue Enzyme replacement therapy Chronic fatigue syndrome Acid alpha-glucosidase Health Medicine Rare diseases
266	HMG Advance Access published May 4, 2011 Human Molecular Genetics, 2011 doi:[removed]hmg/ddr174 R1–R8 Add to Reading List Source URL: amdapompe.ehclients.com Language: English - Date: 2011-05-07 23:33:11 Gene delivery Emerging technologies Molecular biology Applied genetics Biotechnology Glycogen storage disease type II Acid alpha-glucosidase Gene therapy Lysosomal storage disease Biology Medicine Health
267	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 18:14:27 Glycogen storage disease type II Lysosomal storage disease Amyotrophic lateral sclerosis Hypertrophic cardiomyopathy Heart failure Health Rare diseases Medicine
268	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
269	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
270	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 18:38:43 Glycogen storage disease type II Enzyme replacement therapy Lysosomal storage disease Spirometry Amyotrophic lateral sclerosis Fabry disease Alglucosidase alfa ERT Health Medicine Rare diseases

UPDATE