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Inborn error of metabolism
Results: 125

#	Item
71	Minnesota Department of Health[removed]SCAD Add to Reading List Source URL: www.health.state.mn.us Language: English - Date: 2014-04-04 11:40:23 Medicine Carnitine Newborn screening Short-chain acyl-coenzyme A dehydrogenase deficiency Acyl-CoA Inborn error of lipid metabolism Medium-chain acyl-coenzyme A dehydrogenase deficiency Health Rare diseases Chemistry
72	PROPOSED RULE MAKING CR-102 (June[removed]Implements RCW[removed]Do NOT use for expedited rule making Add to Reading List Source URL: www.wsha.org Language: English - Date: 2014-08-05 17:42:21 Genetic genealogy Newborn screening Methylmalonic acidemia Propionic acidemia Isovaleric acidemia Glutaric aciduria type 1 Inborn error of metabolism Galactosemia Maple syrup urine disease Health Rare diseases Medicine
73	FOR IMMEDIATE RELEASE January 7, 2010 Contact: Natasha Bonhomme[removed]x211 Add to Reading List Source URL: www.geneticalliance.org Language: English - Date: 2013-07-24 14:58:31 Medical genetics Medical tests Epidemiology Newborn screening Genetic testing Phenylketonuria Screening Genetic Alliance Inborn error of metabolism Medicine Health Pediatrics
74	Minnesota Department of Health[removed]VLCAD Action required Add to Reading List Source URL: www.health.state.mn.us Language: English - Date: 2014-04-04 11:40:24 Rare diseases Carnitine Very long-chain acyl-coenzyme A dehydrogenase deficiency Newborn screening Hypoglycemia Acyl-CoA Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Medium-chain acyl-coenzyme A dehydrogenase deficiency Inborn error of lipid metabolism Health Medicine Chemistry
75	Time Out for Genetics Webinar Series Genetics Evaluation, Referrals and More– What to Do Next The medical home should consider genetics consultation for all patients with abnormalities of growth or development, with c Add to Reading List Source URL: www.geneticsinprimarycare.org Language: English - Date: 2013-05-21 15:25:03 Medical ethics Cancer research Clinical research Genetic testing Autism Inborn error of metabolism American College of Medical Genetics Mental disorder Medicine Health Medical genetics
76	Medical Information Sheet TYROSINEMIA What is tyrosinemia? Hereditary tyrosinemia is a genetic inborn error of metabolism associated with severe liver disease in infancy. The disease is inherited in an autosomal recessiv Add to Reading List Source URL: www.liver.ca Language: English - Date: 2013-09-26 16:15:11 Tyrosinemia Fumarylacetoacetate hydrolase Type I tyrosinemia Liver Nitisinone Cirrhosis Jaundice Tyrosine Medicine Health Hepatology
77	NEW Nutricia Metabolics_Logo CMYK Add to Reading List Source URL: www.fodsupport.org Language: English - Date: 2014-07-13 19:05:53 Pediatrics Epidemiology Newborn screening Medical genetics Inborn error of metabolism Methylmalonic acidemia Urea cycle disorder Isovaleric acidemia Organic acidemia Health Medicine Rare diseases
78	o ALLIANCE OF GENETIC SUPPORT GROUPS ANNUAL REPORT 1992 REPORT FROM JOAN WEISS, MSW EXECUTIVE DIRECTOR Add to Reading List Source URL: geneticalliance.org Language: English - Date: 2013-07-25 16:04:52 Health Genetic counseling Medical genetics of Jewish people American Society of Human Genetics Genetic disorder National Society of Genetic Counselors Inborn error of metabolism Down syndrome Medicine Medical genetics Biology
79	New Hampshire Newborn Screening Panel As of July 1, 2010 Acronym Argininosuccinic Aciduria ASA Argininemia ARG Add to Reading List Source URL: www.nergg.org Language: English - Date: 2011-08-16 15:44:35 Medical genetics Newborn screening Inborn error of lipid metabolism ACADVL Health Rare diseases Genetic genealogy
80	NEW Nutricia Metabolics_Logo CMYK Add to Reading List Source URL: www.oaanews.org Language: English - Date: 2014-07-13 16:04:14 Pediatrics Epidemiology Newborn screening Medical genetics Inborn error of metabolism Methylmalonic acidemia Urea cycle disorder Isovaleric acidemia Organic acidemia Health Medicine Rare diseases

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