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Isovaleric acidemia
Results: 160

#	Item
121	California Department of Public Health Genetic Disease Screening Program Newborn Screening Program i Add to Reading List Source URL: www.cdph.ca.gov Language: English - Date: 2014-08-13 12:31:27 Rare diseases Newborn screening Fatty-acid metabolism disorder Methylmalonic acidemia Isovaleric acidemia Propionic acidemia Glutaric aciduria type 1 Hyperammonemia Thalassemia Health Genetic genealogy Medical genetics
122	AN ACT RELATING TO HEALTH CARE; AMENDING A SECTION OF THE PUBLIC HEALTH ACT TO REQUIRE TESTING FOR CRITICAL CONGENITAL HEART DISEASE IN NEWBORN INFANTS. BE IT ENACTED BY THE LEGISLATURE OF THE STATE OF NEW MEXICO: Add to Reading List Source URL: www.nmlegis.gov Language: English - Date: 2014-03-03 18:02:18 Pediatrics Newborn screening Methylmalonic acidemia Glutaric aciduria type 1 Biotinidase deficiency Isovaleric acidemia Inborn error of metabolism Galactosemia Congenital hypothyroidism Health Medicine Rare diseases
123	Health Cadham Provincial Laboratory Provincial Programs and Services P.O. Box 8450 Add to Reading List Source URL: www.gov.mb.ca Language: English - Date: 2012-05-08 12:28:03 Pediatrics Epidemiology Newborn screening Mental retardation Metabolism Very long-chain acyl-coenzyme A dehydrogenase deficiency Isovaleric acidemia Methylmalonic acidemia Biotinidase deficiency Health Medicine Rare diseases
124	STATE OF TENNESSEE DEPARTMENT OF HEALTH DIVISION OF LABORATORY SERVICES NEWBORN SCREENING PROGRAM Add to Reading List Source URL: health.state.tn.us Language: English - Date: 2011-02-25 12:37:37 Medical genetics Fatty-acid metabolism disorder Newborn screening Medium-chain acyl-coenzyme A dehydrogenase deficiency Carnitine-acylcarnitine translocase deficiency Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Hyperammonemia Carnitine Isovaleric acidemia Health Rare diseases Genetic genealogy
125	NEWBORN SCREENING IN NEBRASKA Newborn Bloodspot Screening for Metabolic & Inherited Disorders and Early Hearing Detection & Add to Reading List Source URL: dhhs.ne.gov Language: English - Date: 2014-08-22 16:52:20 Pediatrics Epidemiology Newborn screening Inborn errors of carbohydrate metabolism Cystic fibrosis Biotinidase deficiency Methylmalonic acidemia Propionic acidemia Isovaleric acidemia Health Medicine Rare diseases
126	Hygienic Laboratory The University of Iowa For Questions About Resubmission and Result Interpretation Contact Medical Consultants LABORATORY HOSPITAL Add to Reading List Source URL: www.idph.state.ia.us Language: English - Date: 2007-06-25 16:37:50 Rare diseases Fatty-acid metabolism disorder Propionic acidemia Carnitine palmitoyltransferase I Biotinidase deficiency Isovaleric acidemia 3-Methylcrotonyl-CoA carboxylase deficiency Medium-chain acyl-coenzyme A dehydrogenase deficiency 2-Methylbutyryl-CoA dehydrogenase deficiency Health Genetic genealogy Medical genetics
127	Microsoft Word - Haitian_Maine_Insert.doc Add to Reading List Source URL: www.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
128	Microsoft Word - Maine Insert English FINAL.doc Add to Reading List Source URL: www.nergg.org Language: English - Date: 2007-10-17 09:00:27 Medical genetics Newborn screening Isovaleric acidemia Methylmalonic acidemia Glutaric acidemia type 2 Hyperammonemia Propionic acidemia Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Very long-chain acyl-coenzyme A dehydrogenase deficiency Health Rare diseases Genetic genealogy
129	Microsoft Word - Rhode Island insert Khmer.doc Add to Reading List Source URL: www.nergg.org Language: English - Date: 2007-10-17 09:01:33 Medical genetics Newborn screening Isovaleric acidemia Propionic acidemia Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Methylmalonic acidemia Mitochondrial trifunctional protein deficiency Methylcrotonyl-CoA 3-Methylcrotonyl-CoA carboxylase deficiency Health Rare diseases Genetic genealogy
130	Microsoft Word - Vermont Insert English FINAL.doc Add to Reading List Source URL: www.nergg.org Language: English - Date: 2008-04-01 13:39:57 Medical genetics Newborn screening Methylmalonic acidemia Propionic acidemia Isovaleric acidemia 3-Methylcrotonyl-CoA carboxylase deficiency Maple syrup urine disease Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Very long-chain acyl-coenzyme A dehydrogenase deficiency Health Rare diseases Genetic genealogy

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