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Urea cycle
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#	Item
261	PARENT FACT SHEET DISORDER Citrullinemia (CIT) CAUSE CIT occurs when an enzyme called “argininosuccinic acid synthetase” (ASAS), is either missing or not working Add to Reading List Source URL: chfs.ky.gov Language: English - Date: 2014-08-09 04:53:40 Biology Nitrogen metabolism Guanidines Argininosuccinate synthase Enzymes Urea Citrullinemia Arginine Ammonia Chemistry Urea cycle Metabolism
262	Disease Name Citrullinemia type II Alternate name(s) Acronym Add to Reading List Source URL: chfs.ky.gov Language: English - Date: 2014-08-09 06:42:46 Biology Argininosuccinate synthase Citrullinemia Urea cycle disorder Hyperammonemia Argininosuccinic acid Phenylketonuria Arginine Citrulline Urea cycle Metabolism Chemistry
263	Microsoft Word - masterdoc.ammonia.dr3 from ATSDR ac Add to Reading List Source URL: www.atsdr.cdc.gov Language: English - Date: 2011-10-21 16:11:38 Soil biology Metabolism Ammonia Toxicology Nitrogen cycle Nitrogen fixation Urea Nitrification Fertilizer Biology Chemistry Nitrogen metabolism
264	US EPA - Pesticides - Tolerance Reassessment Eligibility Decision for Urea Sulfate Add to Reading List Source URL: www.epa.gov Language: English - Date: 2007-01-31 15:30:59 Excretion Fertilizers Urea Urea cycle Sulfur Food Quality Protection Act Ammonia Solubility Salt Chemistry Nitrogen metabolism Sulfates
265	PDF Document Add to Reading List Source URL: www.hc-sc.gc.ca Language: English - Date: 2013-07-09 12:15:45 Matter Soil biology Metabolism Water treatment Functional groups Ammonia Nitrogen cycle Nitrification Urea Chemistry Biology Nitrogen metabolism
266	Ammonia sanitization of faecal sludge intended for agricultural use Add to Reading List Source URL: www.agrinatura.eu Language: English - Date: 2013-10-03 04:28:53 Urea cycle Sewerage Fertilizers Urea Argininosuccinate synthase Sludge Ammonia Sustainable sanitation Blood urea nitrogen Chemistry Biology Nitrogen metabolism
267	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
268	Volume 6, Issue 1 April 2011 State of Tennessee Department of Health Add to Reading List Source URL: health.state.tn.us Language: English - Date: 2011-04-20 11:54:56 Anatomy Thyroid disease Pediatrics Rare diseases Epidemiology Newborn screening Congenital hypothyroidism Argininosuccinic aciduria Urea cycle disorder Health Biology Urea cycle
269	2010 NBS_AnnualReport - Final.pub Add to Reading List Source URL: health.nv.gov Language: English - Date: 2011-04-04 15:13:34 Rare diseases Epidemiology Newborn screening Inborn errors of carbohydrate metabolism Phenylketonuria Medical genetics Urea cycle disorder Galactosemia Cystic fibrosis Medicine Health Pediatrics
270	PDF Document Add to Reading List Source URL: media.wiley.com Language: English - Date: 2009-01-16 05:04:28 Excretion Fertilizers Nitrogen metabolism Urea Urea cycle Hydrogenation Heinz Falk Dakin oxidation Chemistry Organic reactions Organic chemistry

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