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Enzyme replacement therapy
Results: 54

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31	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
32	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
33	QOL SUCRAID® (sacrosidase) oral solution: DESCRIPTION SUCRAID® (sacrosidase) oral solution is an enzyme replacement therapy for the treatment of genetically Add to Reading List Source URL: www.sucraid.net Language: English - Date: 2014-09-05 11:11:51 Sweeteners Nutrition Hydrolases Carbohydrate chemistry Digestive system Sucraid Sucrose intolerance Sucrase Sacrosidase Chemistry Food and drink Medicine
34	SYNAGEVA BIOPHARMA™ HIGHLIGHTS DATA AT THE NASPGHAN MEETING LEXINGTON, Mass., October 11, [removed]Synageva BioPharma Corp. (Synageva) (NASDAQ:GEVA), a biopharmaceutical company developing therapeutic products for rare Add to Reading List Source URL: www.synageva.com Language: English - Date: 2013-10-11 07:24:04 Lipid storage disorders Lysosomal Acid Lipase Deficiency Wolman disease Cholesteryl ester storage disease Sanfilippo syndrome Lysosomal storage disease Hunter syndrome Enzyme replacement therapy Mucopolysaccharidosis Health Medicine Rare diseases
35	Department of Human Genetics Division of Medical Genetics www.genetics.emory.edu Fabry Disease: Important Facts for Women Add to Reading List Source URL: genetics.emory.edu Language: English - Date: 2009-03-30 13:10:53 Rare diseases Fabry disease Lysosomal storage disease Enzyme replacement therapy Medical genetics Genetic disorder Alpha-galactosidase Fabry Genzyme Medicine Health Lipid storage disorders
36	06 radar report final 4_21.qxd Add to Reading List Source URL: www.fabry.org Language: English - Date: 2014-10-07 04:48:15 Rare diseases Fabry disease Lysosomal storage disease Enzyme replacement therapy Genzyme Fabry Medical genetics Aspirin Medicine Health Lipid storage disorders
37	ORIGINAL CONTRIBUTION Enzyme Replacement Therapy in Fabry Disease A Randomized Controlled Trial Raphael Schiffmann, MD Add to Reading List Source URL: www.fabry.org Language: English - Date: 2014-10-06 21:28:23 Organ failure Pain Kidney diseases Clinical research Fabry disease Neuropathic pain Chronic kidney disease Placebo Renal failure Medicine Health Biology
38	Microsoft PowerPoint[removed]Fabry Registry figure 3.ppt Add to Reading List Source URL: www.fabry.org Language: English - Date: 2014-10-07 11:33:55 Fabry disease Medical terms Pharmacology Disease registry Enzyme replacement therapy Genzyme Fabry Pharmacovigilance Medicine Health Rare diseases
39	Microsoft PowerPoint - Fabry Registry annual report figures redrawn.ppt Add to Reading List Source URL: www.fabry.org Language: English - Date: 2014-10-07 09:12:32 Rare diseases Fabry disease Medical terms Fabry Enzyme replacement therapy Genzyme Patient safety Health Medicine Lipid storage disorders
40	FREG-PT ENROLL MED HST CRF-draft.doc Add to Reading List Source URL: www.fabry.org Language: English - Date: 2014-10-08 20:51:09 Rare diseases Fabry disease Amines Fabry Disease registry Enzyme replacement therapy Brief Pain Inventory Genzyme Alpha-galactosidase Health Medicine Chemistry