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Acyl-CoA
Results: 139

#	Item
61	Microsoft Word - Haitian_Rhode_Island_insert.doc Add to Reading List Source URL: nergg.org Language: English - Date: 2007-10-17 09:01:30 Medical genetics Isovaleric acidemia Propionic acidemia Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Methylcrotonyl-CoA Very long-chain acyl-coenzyme A dehydrogenase deficiency Acyl CoA dehydrogenase Acyl-CoA dehydrogenase Methylmalonic acidemia Health Rare diseases Genetic genealogy
62	Microsoft Word - Haitian_Maine_Insert.doc Add to Reading List Source URL: nergg.org Language: English - Date: 2007-10-17 09:00:32 Rare diseases Isovaleric acidemia Glutaric acidemia type 2 Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Methylmalonic acidemia Glutaric aciduria type 1 Acyl CoA dehydrogenase Very long-chain acyl-coenzyme A dehydrogenase deficiency Propionic acidemia Health Genetic genealogy Medical genetics
63	Microsoft Word - Vermont_Haitian_Insert.doc Add to Reading List Source URL: nergg.org Language: English - Date: 2008-04-01 13:43:08 Medical genetics Methylmalonic acidemia Propionic acidemia Isovaleric acidemia Methylmalonic acid Maple syrup urine disease Acyl CoA dehydrogenase Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Acyl-CoA dehydrogenase Health Rare diseases Genetic genealogy
64	Disease Name MEDIUM CHAIN ACYL-CoA DEHYDROGENASE DEFICIENCY (MCADD) (ACADM DEFICIENCY; MCAD DEFICIENCY; MCADD DEFICIENCY) Fatty acid oxidation defect Classification: Genetic Information Add to Reading List Source URL: www.idph.state.ia.us Language: English - Date: 2007-06-25 16:36:44 Hepatology Metabolism Rare diseases Fatty acids Medium-chain acyl-coenzyme A dehydrogenase deficiency Carnitine Systemic primary carnitine deficiency Newborn screening Hypoglycemia Medicine Health Biology
65	Disease Name SHORT-CHAIN ACYL-COA DEHYDROGENASE DEFICIENCY (SCADD) (ACADS DEFICIENCY; SCADH DEFICIENCY; SCAD DEFICIENCY) Fatty acid oxidation defect Classification: Inheritance: Add to Reading List Source URL: www.idph.state.ia.us Language: English - Date: 2007-06-25 16:37:49 Chemistry Metabolism Fatty acids Short-chain acyl-coenzyme A dehydrogenase deficiency Fatty-acid metabolism disorder Hepatology ACADS Malonyl-CoA decarboxylase deficiency Newborn screening Health Medicine Rare diseases
66	Microsoft Word - Rhode Island Insert English FINAL.doc Add to Reading List Source URL: nergg.org Language: English - Date: 2007-10-17 09:01:25 Medical genetics Newborn screening Isovaleric acidemia Propionic acidemia 3-Methylcrotonyl-CoA carboxylase deficiency Methylmalonic acidemia Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Biotinidase deficiency Very long-chain acyl-coenzyme A dehydrogenase deficiency Health Rare diseases Genetic genealogy
67	Microsoft Word - Haitian_New_Hampshire_Insert.doc Add to Reading List Source URL: nergg.org Language: English - Date: 2007-10-17 09:01:10 Medical genetics Propionic acidemia Methylcrotonyl-CoA carboxylase Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Isovaleric acidemia Methylcrotonyl-CoA Acyl CoA dehydrogenase Malonyl-CoA decarboxylase deficiency Very long-chain acyl-coenzyme A dehydrogenase deficiency Health Rare diseases Genetic genealogy
68	Short-chain acyl-CoA Dehydrogenase Deficiency (SCAD) What is a positive newborn screen? Newborn screening is done on tiny samples of blood taken from your baby’s heel 24 to 36 hours after birth. The blood is tested for Add to Reading List Source URL: www.michigan.gov Language: English - Date: 2012-12-07 14:06:00 Epidemiology Newborn screening Pediatrics Short-chain acyl-coenzyme A dehydrogenase deficiency Infant Screening Health Rare diseases Medicine
69	Long-chain L-3-hydroxy acyl-CoA Dehydrogenase Deficiency (LCHAD) Trifunctional Protein Deficiency (TFP) What is a positive newborn screen? Newborn screening is done on tiny samples of blood taken from your baby’s heel Add to Reading List Source URL: www.michigan.gov Language: English - Date: 2012-12-07 10:42:23 Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Newborn screening Mitochondrial trifunctional protein deficiency Fatty-acid metabolism disorder Mitochondrial trifunctional protein Health Medicine Rare diseases
70	Medium-Chain Acyl-CoA Dehydrogenase Deficiency (MCAD) What is a positive newborn screen? Newborn screening is done on tiny samples of blood taken from your baby’s heel 24 to 36 hours after birth. The blood is tested fo Add to Reading List Source URL: www.michigan.gov Language: English - Date: 2012-12-07 14:13:24 Medium-chain acyl-coenzyme A dehydrogenase deficiency Newborn screening Infancy Screening Infant Health Medicine Pediatrics

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