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Glycogen
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#	Item
361	FY12 IT Plan Fiscal Year 2012 General Services Department IT Plan “INNOVATION, DEFINED PROCESS, RESULTS” Add to Reading List Source URL: www.generalservices.state.nm.us Language: English - Date: 2011-06-23 13:19:48 Standards Glycogen storage disease type I Capability Maturity Model Corporate governance of information technology Information Technology Infrastructure Library Product management Technology Management Information technology management Software development process Method engineering
362	Parent Fact Sheet Disorder Long Chain 3-hydroxyacyl-CoA dehydrogenase deficiency (LCHADD) Cause People with LCHADD have problems breaking down a fatty acid into energy for the body. LCHADD occurs when an enzyme called lo Add to Reading List Source URL: chfs.ky.gov Language: English - Date: 2014-08-09 10:55:30 Diabetes Hepatology Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Hypoglycemia 3-hydroxyacyl-CoA dehydrogenase 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Blood sugar Very long-chain acyl-coenzyme A dehydrogenase deficiency Glycogen storage disease type I Medicine Health Biology
363	As of[removed]JISC Infrastructure and future We have 2 main servers at GSD, one is a true production, the other serves as Virtual production, test and dev environments on that box. The load balancing between Production b Add to Reading List Source URL: nmsc.unm.edu Language: English - Date: 2013-01-08 17:19:39 Load balancing Inborn errors of carbohydrate metabolism Hepatology Glycogen storage disease type I
364	Sports Nutrition For Young Adults 3: Eating Before & Between Athletic Events - HE-0750 Add to Reading List Source URL: www.aces.edu Language: English - Date: 2013-05-21 21:27:34 Biology Diets Dietary supplements Self-care Glycogen Dietary fiber Sports nutrition Fasting Hypoglycemia Medicine Health Nutrition
365	HIG H LIG H TS O F PRES CRIBING INFO RMATIO N Th e s e hig hlig hts do n ot include a ll the information needed to u se MYO ZYME s afe ly and effectively . See full prescribing i nformation for MYO ZYME. MYO ZYME® (a l Add to Reading List Source URL: www.accessdata.fda.gov Language: English - Date: 2014-05-27 14:10:42 Glycogen storage disease type II Genzyme Allergy Medicine Health Alglucosidase alfa
366	Coffee consumption and risk chronic diseases: the epidemiological evidence Add to Reading List Source URL: ods.od.nih.gov Language: English - Date: 2013-12-09 15:34:14 Caffeine Nutrition Xanthines Exercise physiology Energy drink Glycogen Taurine Decaffeination Chemistry Biology Medicine
367	Energy Availability and Alcohol-Related Liver Pathology Add to Reading List Source URL: pubs.niaaa.nih.gov Language: English - Date: 2004-09-22 17:26:34 Cellular respiration Exercise physiology Metabolism Metabolic pathways Nutrition Glycolysis Alcohol dehydrogenase Adenosine triphosphate Glycogen Biology Biochemistry Chemistry
368	JANUARY[removed]UNDERSTANDING POMPE DISEASE Pompe (POM-pay) disease, also known as glycogen storage disease type II or acid maltase deficiency, is a Add to Reading List Source URL: www.niams.nih.gov Language: English - Date: 2013-05-22 13:44:51 Lysosomal storage diseases Glycogen storage disease type II Hepatology National Institutes of Health National Institute of Arthritis and Musculoskeletal and Skin Diseases Acid alpha-glucosidase Alglucosidase alfa Arthritis Weakness Medicine Health Rare diseases
369	NIAMS IRPartners Spring/Summer[removed]A newsletter for Add to Reading List Source URL: www.niams.nih.gov Language: English - Date: 2011-10-31 10:43:00 Autoimmune diseases Rare diseases National Institute of Arthritis and Musculoskeletal and Skin Diseases Arthritis Rheumatology NIH Intramural Research Program Glycogen storage disease type II Arthritis Foundation Rheumatoid arthritis Health Medicine National Institutes of Health
370	Disease Name Hydroxymethylglutaric aciduria (3-OH 3-CH3 glutaric aciduria) Alternate name(s) Add to Reading List Source URL: chfs.ky.gov Language: English - Date: 2014-08-08 19:53:26 3-hydroxy-3-methylglutaryl-CoA lyase Rare diseases Hypoglycemia Pediatrics Glutaric aciduria type 1 Glycogen storage disease type I Health Medicine 3-hydroxy-3-methylglutaryl-CoA lyase deficiency

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