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Organic acidemia
Results: 73

#	Item
1	TIMELINESS OF NEWBORN SCREENING – DACHDNC LABORATORY STANDARDS AND PROCEDURES SUBCOMMITTEE DRAFT FINDINGS AND PROPOSED RECOMMENDATIONS Kellie Kelm, PhD Add to Reading List Source URL: www.hrsa.gov Language: English Newborn screening Isovaleric acidemia Galactosemia Methylmalonic acidemia Propionic acidemia Malonyl-CoA decarboxylase deficiency Inborn error of metabolism Argininosuccinic aciduria Organic acidemia Health Rare diseases Medicine
2	Volume 6, Issue 3 October 2011 State of Tennessee Add to Reading List Source URL: health.tn.gov Language: English - Date: 2011-10-04 10:57:09 Health sciences Pediatrics Epidemiology Newborn screening Medical specialties Amino acid Organic acidemia Maple syrup urine disease Carnitine Health Medicine Rare diseases
3	Microsoft Word - mso8C.doc Add to Reading List Source URL: health.mo.gov Language: English - Date: 2007-11-28 16:03:24 Medical genetics Glutaric aciduria type 1 Newborn screening Organic acidemia Glutaric acidemia type 2 Propionic acidemia Health Rare diseases Genetic genealogy
4	Volume 6, Issue 3 October 2011 State of Tennessee Add to Reading List Source URL: health.state.tn.us Language: English - Date: 2011-10-04 10:57:09 Health sciences Pediatrics Epidemiology Newborn screening Medical specialties Amino acid Organic acidemia Maple syrup urine disease Carnitine Health Medicine Rare diseases
5	Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCAD) Add to Reading List Source URL: health.mo.gov Language: English - Date: 2009-02-03 16:51:33 Newborn screening Thiolase Organic acidemia Beta-ketothiolase deficiency Propionic acidemia Health Rare diseases Medicine
6	Microsoft Word - Organic_Acidemias.doc Add to Reading List Source URL: health.state.tn.us Language: English - Date: 2007-05-01 15:47:00 Genetic genealogy Isovaleric acidemia Propionic acidemia Organic acidemia Newborn screening Methylmalonic acidemia Malonyl-CoA decarboxylase deficiency 3-Methylcrotonyl-CoA carboxylase deficiency Medical genetics Health Rare diseases Medicine
7	Isovaleric Acidemia (IVA) An organic acid disorder What is it? Isovaleric Acidemia (also known as IVA) is an inherited organic acid disorder. People with organic acid disorders, like IVA, cannot properly break down certa Add to Reading List Source URL: health.mo.gov Language: English - Date: 2007-09-13 16:17:12 Medical genetics Isovaleric acidemia Newborn screening Organic acidemia Propionic acidemia Methylmalonic acidemia Health Rare diseases Genetic genealogy
8	Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCAD) Add to Reading List Source URL: health.mo.gov Language: English - Date: 2009-02-03 16:51:01 Medical genetics Methylmalonic acidemia Propionic acidemia Organic acidemia Newborn screening Methylmalonic acid Malonyl-CoA decarboxylase deficiency Vitamin B12 Isovaleric acidemia Health Rare diseases Genetic genealogy
9	Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCAD) Add to Reading List Source URL: health.mo.gov Language: English - Date: 2009-02-03 16:52:18 Medical genetics Newborn screening Organic acidemia 2-Methylbutyryl-CoA dehydrogenase deficiency Methylmalonic acidemia Health Rare diseases Genetic genealogy
10	(ISOVALERIC ACID CoA DEHYDROGENASE DEFICIENCY; IVA; IVD) Add to Reading List Source URL: health.state.tn.us Language: English - Date: 2007-05-01 10:03:12 Medical genetics Organic acidemia Isovaleric acidemia Propionic acidemia Newborn screening Methylmalonic acidemia Glutaric aciduria type 1 Malonyl-CoA decarboxylase deficiency 3-Methylcrotonyl-CoA carboxylase deficiency Health Rare diseases Genetic genealogy