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Citrullinemia
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1	STATE of MINNESOTA WHEREAS: Urea Cycle Disorders are rare diseases, occurring at an overall incidence of at least 1 in 35,000 births, and likely higher. Newborns affected with Urea Cycle Disorders can Add to Reading List Source URL: mn.gov Language: English - Date: 2015-05-26 10:33:22 Biology Nitrogen metabolism Rare diseases Urea cycle disorder Urea Newborn screening Argininemia Citrullinemia Health Metabolism Urea cycle
2	UCDC Newsletter_4.22.13_Final.pub Add to Reading List Source URL: www.rarediseasesnetwork.org Language: English - Date: 2013-04-23 17:35:32 Health Urea cycle disorder Ornithine transcarbamylase deficiency Argininosuccinic aciduria Hyperammonemia Ornithine translocase deficiency Arginase Citrullinemia N-Acetylglutamate synthase deficiency Urea cycle Metabolism Biology
3	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
4	Citrullinemia (CIT) (metabolic condition: amino acid disorder) Also known as: • citrullinuria Add to Reading List Source URL: www.albertahealthservices.ca Language: English - Date: 2013-09-16 18:05:06 Biology Nitrogen metabolism Urea cycle disorder Hyperammonemia Argininosuccinate synthase Amino acid Medical genetics Citrulline Arginine Chemistry Urea cycle Metabolism
5	NEWBORN SCREENING FACT SHEET ASAS Deficiency (Citrullinemia) also milder forms that start later in infancy or childhood. There is also a rare adult form more common in people of Japanese heritage. Add to Reading List Source URL: www.ndhealth.gov Language: English - Date: 2009-02-19 11:31:53 Health Nitrogen metabolism Citrullinemia Argininosuccinate synthase Urea cycle disorder Newborn screening Phenylketonuria Ammonia Citrulline Chemistry Urea cycle Metabolism
6	Microsoft Word - ass_type2 Add to Reading List Source URL: www.idph.state.ia.us Language: English - Date: 2007-06-25 16:35:50 Biology Urea cycle Citrullinemia Argininosuccinate synthase Urea cycle disorder Cholestasis Jaundice Hyperammonemia Citrin Medicine Health Hepatology
7	Disease Name CLASSIC CITRULLINEMIA (ASS) (CITRULLINEMIA, TYPE I; CTLN1; ARGININOSUCCINATE SYNTHETASE DEFICIENCY; ASS DEFICIENCY) Urea cycle defect Classification: Add to Reading List Source URL: www.idph.state.ia.us Language: English - Date: 2007-06-25 16:35:49 Biology Citrullinemia Argininosuccinate synthase Urea cycle disorder Hyperammonemia Argininosuccinic acid Arginine Newborn screening Citrulline Urea cycle Metabolism Chemistry
8	CLASSIC CITRULLINEMIA (ASS) REFERENCES (CITRULLINEMIA, TYPE I; CTLN1; ARGININOSUCCINATE SYNTHETASE DEFICIENCY; ASS DEFICIENCY) 1. 2. Add to Reading List Source URL: www.idph.state.ia.us Language: English - Date: 2007-06-25 16:35:49 Biology Health Argininosuccinate synthase Citrin Urea cycle disorder Hyperammonemia Saheki Ornithine transcarbamylase deficiency Urea cycle Metabolism Citrullinemia
9	Microsoft Word - ass_type2_ref Add to Reading List Source URL: www.idph.state.ia.us Language: English - Date: 2007-06-25 16:35:51 Biology Argininosuccinate synthase Citrin Planetary science Urea cycle disorder Hyperammonemia Saheki Urea cycle Metabolism Citrullinemia
10	Citrullinemia (CIT) What is a positive newborn screen? Newborn screening is done on tiny samples of blood taken from your baby’s heel 24 to 36 hours after birth. The blood is tested for rare, hidden disorders that may Add to Reading List Source URL: www.michigan.gov Language: English - Date: 2012-12-07 10:31:38 Biology Citrullinemia Rare diseases Argininosuccinate synthase Newborn screening Citrulline Screening Protein Infant Health Urea cycle Medicine

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