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Urea cycle disorder
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61	February 13, 2013 The Honorable Mary K. Wakefield, PhD, RN Administrator U.S. Health Resources and Services Administration 5600 Fishers Lane Rockville, MD 20857 Add to Reading List Source URL: mda.org Language: English - Date: 2013-04-10 17:49:53 Epidemiology Newborn screening Pediatrics March of Dimes Association of Public Health Laboratories Medical specialties Screening Urea cycle disorder Infant Medicine Health Rare diseases
62	Tennessee Department of Health Public Health Laboratories Newsletter Susan R. Cooper, MSN, RN Commissioner of Health David L. Smalley, Ph.D., M.S.S., BCLD Add to Reading List Source URL: health.state.tn.us Language: English - Date: 2010-10-05 11:11:45 Urea cycle Rare diseases Escherichia coli Enterobacteria Gram-negative bacteria Argininosuccinic aciduria Escherichia coli O157:H7 Urea cycle disorder Argininosuccinate lyase Health Medicine Biology
63	AAP Screening-ScreenMaterials-newborn screening disorders.pdf Add to Reading List Source URL: www.medicalhomeinfo.org Language: English - Date: 2010-02-08 16:26:00 Rare diseases Mental retardation Epidemiology Newborn screening Inborn errors of carbohydrate metabolism Phenylketonuria Urea cycle disorder Congenital hypothyroidism Biotinidase deficiency Health Medicine Pediatrics
64	Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCAD) Add to Reading List Source URL: health.mo.gov Language: English - Date: 2009-02-03 16:51:23 Medical genetics Argininosuccinic aciduria Urea cycle disorder Newborn screening Argininosuccinate lyase Carbamoyl phosphate synthetase I deficiency Glutaric acidemia type 2 Health Rare diseases Genetic genealogy
65	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: 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
66	Volume 94 No. 5 q Zebras May 2011 Add to Reading List Source URL: www.rimed.org Language: English - Date: 2011-05-12 16:26:23 Epidemiology Pervasive developmental disorders Autism Medical specialties Urea cycle disorder Newborn screening Medical genetics Argininosuccinic aciduria Epidemiology of autism Medicine Health Rare diseases
67	Disease Name Citrullinemia type I Alternate name(s) Acronym Add to Reading List Source URL: chfs.ky.gov Language: English - Date: 2014-08-09 12:23:50 Biology Argininosuccinate synthase Citrullinemia Urea cycle disorder Hyperammonemia Argininosuccinic acid Phenylketonuria Arginine Citrulline Urea cycle Metabolism Chemistry
68	PARENT FACT SHEET DISORDER Argininosuccinic Acidemia (ASA) CAUSE ASA occurs when an enzyme called argininosuccinic acid lyase is either missing or not working Add to Reading List Source URL: chfs.ky.gov Language: English - Date: 2014-08-09 11:26:15 Biology Argininosuccinic aciduria Arginine Urea Ammonia Argininosuccinic acid Protein Urea cycle disorder Ornithine transcarbamylase deficiency Chemistry Urea cycle Metabolism
69	Disease Name Argininosuccinic Acidemia Alternate name(s) Acronym Add to Reading List Source URL: chfs.ky.gov Language: English - Date: 2014-08-09 08:46:16 Health Urea cycle disorder Argininosuccinate synthase Argininosuccinate lyase Argininosuccinic aciduria Argininosuccinic acid Citrullinemia Trichorrhexis nodosa Hyperammonemia Urea cycle Metabolism Biology
70	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

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