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Citrullinemia
Results: 30

#	Item
11	2012 Minnesota Department of Health (sit-roo-lin-ee-me-ah) POSITIVE NEWBORN SCREEN Add to Reading List Source URL: www.health.state.mn.us Language: English - Date: 2014-04-04 11:40:10 Medicine Citrullinemia Argininosuccinate synthase Urea cycle disorder Newborn screening Citrulline Screening Urea cycle Health Metabolism
12	Minnesota Department of Health[removed]POSITIVE NEWBORN SCREEN Add to Reading List Source URL: www.health.state.mn.us Language: English - Date: 2014-04-04 11:40:18 Biology Nitrogen metabolism Rare diseases Hyperammonemia Citrullinemia Urea cycle disorder Argininosuccinate synthase Newborn screening Ammonia Chemistry Urea cycle Metabolism
13	Microsoft Word - Citrullinemia[removed]doc Add to Reading List Source URL: www.newbornscreening.info Language: English - Date: 2013-07-18 20:53:24 Chemistry Nitrogen metabolism Rare diseases Citrullinemia Argininosuccinate synthase Urea cycle disorder Newborn screening Amino acid Citrulline Health Urea cycle Metabolism
14	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.tn.gov 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
15	Citrullinemia (CIT) A urea cycle disorder What is it? Citrullinemia (also known as argininosuccinic acid synthetase deficiency (CIT)) is a urea cycle disorder. People with urea cycle disorders, like CIT, cannot properly Add to Reading List Source URL: www.health.mo.gov Language: English - Date: 2007-09-13 15:35:42 Rare diseases Urea cycle disorder Citrullinemia Newborn screening Medical genetics Argininosuccinate synthase Argininosuccinic aciduria Carbamoyl phosphate synthetase I deficiency Medicine Health Urea cycle
16	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: www.chfs.ky.gov Language: English - Date: 2014-09-12 02:05:21 Biology Nitrogen metabolism Guanidines Argininosuccinate synthase Enzymes Urea Citrullinemia Arginine Ammonia Chemistry Urea cycle Metabolism
17	Disease Name Citrullinemia type II Alternate name(s) Acronym Add to Reading List Source URL: www.chfs.ky.gov Language: English - Date: 2014-09-11 03:36:05 Biology Argininosuccinate synthase Citrullinemia Urea cycle disorder Hyperammonemia Argininosuccinic acid Phenylketonuria Arginine Citrulline Urea cycle Metabolism Chemistry
18	Disease Name Argininosuccinic Acidemia Alternate name(s) Acronym Add to Reading List Source URL: www.chfs.ky.gov Language: English - Date: 2014-09-09 06:57:25 Health Urea cycle disorder Argininosuccinate synthase Argininosuccinate lyase Argininosuccinic aciduria Argininosuccinic acid Citrullinemia Trichorrhexis nodosa Hyperammonemia Urea cycle Metabolism Biology
19	Disease Name Citrullinemia type I Alternate name(s) Acronym Add to Reading List Source URL: www.chfs.ky.gov Language: English - Date: 2014-09-09 05:10:27 Biology Argininosuccinate synthase Citrullinemia Urea cycle disorder Hyperammonemia Argininosuccinic acid Phenylketonuria Arginine Citrulline Urea cycle Metabolism Chemistry
20	Disease Name: CITRULLINEMIA, TYPE 2 (CITRULLINEMIA, TYPE II, ADULT-ONSET; CTLN2; CITRULLINEMIA, TYPE II, NEONATAL-ONSET; CHOLESTASIS, NEONATAL INTRAHEPATIC, CAUSED BY CITRIN DEFICIENCY) Add to Reading List Source URL: public.health.oregon.gov Language: English - Date: 2011-01-16 02:52:28 Medicine Citrullinemia Argininosuccinate synthase Citrin Hepatology Urea cycle disorder Hyperammonemia Saheki Liver disease Biology Urea cycle Metabolism

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