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Propionic acidemia
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121	NEWBORN SCREENING CONFIRMED CASE REPORT PRIMARY PANEL OF 29 DISORDERS DOB[removed] – [removed]Disorder Abbreviation Add to Reading List Source URL: www.azdhs.gov Language: English - Date: 2012-04-12 12:46:51 Medical genetics Newborn screening Methylmalonic acidemia Propionic acidemia Isovaleric acidemia Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Maple syrup urine disease Medium-chain acyl-coenzyme A dehydrogenase deficiency Methylmalonic acid Health Rare diseases Genetic genealogy
122	OFFICE OF NEWBORN SCREENING 2008 CONFIRMED CASE REPORT PRIMARY PANEL OF 28 BLOODSPOT DISORDERS DISORDER ANALYTE Add to Reading List Source URL: www.azdhs.gov Language: English - Date: 2012-04-12 12:46:54 Medical genetics Newborn screening Propionic acidemia Methylmalonic acidemia Isovaleric acidemia Biotinidase deficiency Glutaric aciduria type 1 Medium-chain acyl-coenzyme A dehydrogenase deficiency Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Health Rare diseases Genetic genealogy
123	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
124	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
125	Arizona Administrative Register / Secretary of State Notices of Final Rulemaking NOTICES OF FINAL RULEMAKING The Administrative Procedure Act requires the publication of the final rules of the state’s agencies. Final r Add to Reading List Source URL: www.azdhs.gov Language: English - Date: 2014-05-29 18:43:12 Pediatrics Newborn screening Biotinidase deficiency Methylmalonic acidemia Congenital hypothyroidism Propionic acidemia Galactosemia Health care provider 3-Methylcrotonyl-CoA carboxylase deficiency Health Medicine Rare diseases
126	HEEL STICK NEWS RAISING AWARENESS OF IOWA NEONATAL METABOLIC SCREENING PROGRAM (INMSP) OCTOBER 2003 “I like to think of Add to Reading List Source URL: www.idph.state.ia.us Language: English - Date: 2007-06-25 16:37:22 Rare diseases Pediatrics Newborn screening Galactosemia Fatty-acid metabolism disorder Inborn error of metabolism Biotinidase deficiency Propionic acidemia Hyperammonemia Health Medicine Genetic genealogy
127	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
128	Microsoft Word - New Hampshire Insert English FINAL.doc Add to Reading List Source URL: www.nergg.org Language: English - Date: 2007-10-17 09:01:06 Medical genetics Newborn screening 3-Methylcrotonyl-CoA carboxylase deficiency Methylcrotonyl-CoA carboxylase Propionic acidemia Biotinidase deficiency Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Thiolase Very long-chain acyl-coenzyme A dehydrogenase deficiency Health Rare diseases Genetic genealogy
129	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
130	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

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