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Acyl-CoA dehydrogenase
Results: 122

#	Item
21	Mitochondrial Carbonic Anhydrase VA Deficiency Resulting from CA5A Alterations Presents with Hyperammonemia in Early Childhood Add to Reading List Source URL: www.tidebc.org Language: English - Date: 2014-02-13 12:45:25 Enzymes Carbonic anhydrase Carbonic anhydrase inhibitors Hyperammonemia Propionyl-CoA carboxylase Pyruvate carboxylase Biotin Medium-chain acyl-coenzyme A dehydrogenase deficiency Acetazolamide Chemistry Medicine Health
22	Microsoft Word - SCADD update 2011.doc Add to Reading List Source URL: www.newbornscreening.info Language: English - Date: 2011-04-27 16:22:45 Chemistry Fatty-acid metabolism disorder Newborn screening Short-chain acyl-coenzyme A dehydrogenase deficiency Acyl CoA dehydrogenase ACADS Carnitine Very long-chain acyl-coenzyme A dehydrogenase deficiency Fatty acid metabolism Health Rare diseases Medicine
23	doi:[removed]j.ymgme[removed] Add to Reading List Source URL: www.fodsupport.org Language: English - Date: 2012-05-31 13:40:39 Medicine ACADS Fatty-acid metabolism disorder Malonyl-CoA decarboxylase deficiency Newborn screening Acyl CoA dehydrogenase Acyl-CoA Carnitine Thiolase Health Rare diseases Chemistry
24	Illness Protocol Example For Medium-Chain Acyl-CoA Dehydrogenase (MCAD) Deficiency For Infants and Young Children Clinical Presentation: Anorexia, Vomiting, Lethargy, +/- Hypoglycemia, Reye-like syndrome Add to Reading List Source URL: fodsupport.org Language: English - Date: 2012-05-31 13:41:17 Health Blood sugar Anatomy Glycogen storage disease type I Diabetic hypoglycemia Medicine Diabetes Hypoglycemia
25	A rough guide to Acylcarnitines Roy Talbot & Nigel Manning [removed] Dept. of Clinical Chemistry, Add to Reading List Source URL: www.fodsupport.org Language: English - Date: 2012-05-31 13:41:07 Tandem mass spectrometry Medium-chain acyl-coenzyme A dehydrogenase deficiency Triple quadrupole mass spectrometer CH2 Quadrupole mass analyzer Gas chromatography–mass spectrometry Acyl-CoA Electrospray ionization Coenzyme A Chemistry Mass spectrometry Carnitine
26	MS/MS-BASED NEWBORN AND FAMILY SCREENING DETECTS ASYMPTOMATIC PATIENTS WITH VERY-LONG-CHAIN ACYL-COA DEHYDROGENASE DEFICIENCY UTE SPIEKERKOETTER, MD, BIN SUN, MD, THOMAS ZYTKOVICZ, PHD, RONALD WANDERS, PHD, ARNOLD W. STR Add to Reading List Source URL: www.fodsupport.org Language: English - Date: 2012-05-31 13:41:14 Rare diseases Medium-chain acyl-coenzyme A dehydrogenase deficiency Newborn screening Very long-chain acyl-coenzyme A dehydrogenase deficiency Fatty-acid metabolism disorder Acyl CoA dehydrogenase Phenylketonuria Mitochondrial trifunctional protein Inborn error of lipid metabolism Health Genetic genealogy Medical genetics
27	EXPANDED NEWBORN SCREENING 2005 to 2009 MISSED OPPORTUNITIES -- POTENTIAL LEGAL CLAIMS Over the past five years, it’s become clear that many children who should have had the benefit of expanded screening did not. By ea Add to Reading List Source URL: fodsupport.org Language: English - Date: 2012-05-31 13:41:05 Medical genetics Newborn screening Propionic acidemia Methylmalonic acidemia Isovaleric acidemia Very long-chain acyl-coenzyme A dehydrogenase deficiency Glutaric aciduria type 1 Malonyl-CoA decarboxylase deficiency Medium-chain acyl-coenzyme A dehydrogenase deficiency Health Rare diseases Genetic genealogy
28	Newborn_Screening_C4.indd Add to Reading List Source URL: www.mayomedicallaboratories.com Language: English - Date: 2014-10-28 14:15:46 Medicine Epidemiology Newborn screening Pediatrics Carnitine Isobutyryl-CoA Acyl CoA dehydrogenase Ethylmalonic encephalopathy Health Chemistry Rare diseases
29	MCAD: Sudden and Unexpected Death of a 45-year-old Woman Kimiyo Raymond, MD, Allen E. Bale, MD, C. Allan Barnes, MD, Piero Rinaldo, MD, PhD Medium-chain acyl-CoA dehydrogenase (MCAD) deficiency is the most common fatty a Add to Reading List Source URL: www.fodsupport.org Language: English - Date: 2012-05-31 13:41:07 Metabolism Fatty acids Fatty-acid metabolism disorder Hepatology Medium-chain acyl-coenzyme A dehydrogenase deficiency Rare diseases Carnitine Fatty acid metabolism Newborn screening Health Medicine Chemistry
30	Example of VLCAD Protocol To Whom It May Concern: Re: (Name of child) Date of Birth: _____________ is a __ year old boy with very long chain acyl-CoA dehydrogenase (VLCAD) deficiency, an inborn error of mitochondrial fat Add to Reading List Source URL: fodsupport.org Language: English - Date: 2012-05-31 13:41:18 Health Nephrology Very long-chain acyl-coenzyme A dehydrogenase deficiency Acute kidney injury Anuria Renal failure Heart failure Myoglobinuria Cardiomyopathy Medicine Anatomy Organ failure

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