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Maple syrup urine disease
Results: 95

#	Item
81	Vermont Newborn Screening Program Add to Reading List Source URL: www.nergg.org Language: English - Date: 2008-04-01 13:45:35 Medical genetics Newborn screening Methylmalonic acidemia Propionic acidemia Isovaleric acidemia Maple syrup urine disease Methylmalonic acid Very long-chain acyl-coenzyme A dehydrogenase deficiency Thiolase Health Rare diseases Genetic genealogy
82	Microsoft Word - Vermont_Haitian_Insert.doc Add to Reading List Source URL: www.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
83	Microsoft Word - Disorder list Jan 10 Add to Reading List Source URL: www.azdhs.gov Language: English - Date: 2012-04-12 12:47:40 Medical genetics Newborn screening Propionic acidemia Methylmalonic acidemia Isovaleric acidemia Fatty-acid metabolism disorder 3-Methylcrotonyl-CoA carboxylase deficiency Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency Maple syrup urine disease Health Rare diseases Genetic genealogy
84	MISSOURI DEPARTMENT OF HEALTH Add to Reading List Source URL: health.mo.gov Language: English - Date: 2013-08-16 15:32:03 Medical genetics Methylmalonic acidemia Isovaleric acidemia Propionic acidemia Glutaric aciduria type 1 Maple syrup urine disease University of Missouri Health Care Medicaid Department of Health Health Rare diseases Genetic genealogy
85	Parent Fact Sheet Disorder Propionic Acidemia (PA) Cause Propionic Acidemia (PA) is one type of organic acid disorder. People with PA have problems breaking down and using certain amino acids from the foods they eat. PA Add to Reading List Source URL: chfs.ky.gov Language: English - Date: 2014-08-09 11:33:50 Genetic genealogy Propionic acidemia Carnitine Acidosis Maple syrup urine disease Methylmalonic acidemia Health Rare diseases Medicine
86	Cardinal Glennon Children’s Hospital Add to Reading List Source URL: health.mo.gov Language: English - Date: 2007-09-14 07:52:40 Maple syrup urine disease Branched-chain amino acids Leucine Newborn screening Medical genetics Amino acid Recessive Branched-chain alpha-keto acid dehydrogenase complex Health Medicine Rare diseases
87	Microsoft Word - Maple Syrup Urine Disease.doc Add to Reading List Source URL: chfs.ky.gov Language: English - Date: 2014-08-09 07:19:13 Chemistry Genetic genealogy Leucine Amino acid Protein Health Rare diseases Maple syrup urine disease
88	Microsoft Word - Amino_Acidemias.doc Add to Reading List Source URL: health.state.tn.us Language: English - Date: 2007-05-01 14:35:52 Medical genetics Maple syrup urine disease Glycine encephalopathy Newborn screening Phenylketonuria Amino acid Phenylalanine Organic acidemia Propionic acidemia Health Rare diseases Genetic genealogy
89	AMINO ACID DISORDERS Karla J Matteson, PhD, FACMG University of Tennessee Genetic Center, Knoxville Outcome without screening: The amino acid disorders are a collection of disorders that involve enzyme deficiencies that Add to Reading List Source URL: health.state.tn.us Language: English - Date: 2006-10-30 12:08:43 Rare diseases Phenylketonuria Newborn screening Urea cycle disorder Hypermethioninemia Maple syrup urine disease Amino acid Protein Citrullinemia Health Medicine Genetic genealogy
90	Maple Syrup Urine Disease (MSUD) What is maple syrup urine disease (MSUD)? Maple syrup urine disease (also known as MSUD) is an inherited condition that affects the way a person’s body uses certain parts of protein. A Add to Reading List Source URL: health.state.tn.us Language: English - Date: 2007-05-01 15:44:42 Medicine Maple syrup urine disease BCKDHB Newborn screening Leucine Thiamine Organic acidemia Hypoglycemia Branched-chain alpha-keto acid dehydrogenase complex Health Rare diseases Chemistry