Tyrosinemia - PDFSEARCH.IO - Document Search Engine

Tyrosinemia
Results: 27

#	Item
1	Molecular Genetics and Metabolism–75 Contents lists available at ScienceDirect Molecular Genetics and Metabolism journal homepage: www.elsevier.com/locate/ymgme Add to Reading List Source URL: www.hrsa.gov Language: English Newborn screening Pediatrics Standards organizations Tyrosinemia Type I tyrosinemia Medical genetics National Institute of Standards and Technology Tyrosine Medicine Health Epidemiology
2	Molecular Genetics and Metabolism–75 Contents lists available at ScienceDirect Molecular Genetics and Metabolism journal homepage: www.elsevier.com/locate/ymgme Add to Reading List Source URL: www.hrsa.gov Language: English Newborn screening Pediatrics Standards organizations Tyrosinemia Type I tyrosinemia Medical genetics National Institute of Standards and Technology Tyrosine Medicine Health Epidemiology
3	DEPARTMENT OF HEALTH AND HUMAN SERVICES Discretionary Advisory Committee on Heritable Disorders in Newborns and Children 5600 Fishers Lane, Room 18A19 Rockville, Marylandwww.hrsa.gov/heritabledisorderscommittee Add to Reading List Source URL: www.hrsa.gov Language: English Newborn screening Pediatrics Tyrosinemia Fumarylacetoacetate hydrolase Screening Infant Health Medicine Epidemiology
4	Medical Information Sheet TYROSINEMIA What is tyrosinemia? Hereditary tyrosinemia is a genetic inborn error of metabolism associated with severe liver disease in infancy. The disease is inherited in an autosomal recessiv Add to Reading List Source URL: www.liver.ca Language: English - Date: 2012-11-22 19:06:20 Tyrosinemia Fumarylacetoacetate hydrolase Type I tyrosinemia Liver Nitisinone Cirrhosis Jaundice Tyrosine Medicine Health Hepatology
5	Medical Information Sheet TYROSINEMIA What is tyrosinemia? Hereditary tyrosinemia is a genetic inborn error of metabolism associated with severe liver disease in infancy. The disease is inherited in an autosomal recessiv Add to Reading List Source URL: liver.ca Language: English - Date: 2013-09-26 16:15:11 Tyrosinemia Fumarylacetoacetate hydrolase Type I tyrosinemia Liver Nitisinone Cirrhosis Jaundice Tyrosine Medicine Health Hepatology
6	Hereditary tyrosinemia is due to a defect in an enzyme metabolizing a protein building-block (tyrosine). Since tyrosinemia is particularly common in northern Quebec, doctors test the blood of every newborn baby in the pr Add to Reading List Source URL: liver.ca Language: English - Date: 2012-11-22 19:06:52 Biliary atresia Neonatal jaundice Liver Hepatitis Bilirubin Bile duct Hepato-biliary diseases Medicine Hepatology Jaundice
7	September 20, 2013 Kellie Kelm, Ph.D. – Chair Susan Tanksley, Ph.D. – Co-chair Priorities for Lab Subcommittee Add to Reading List Source URL: www.hrsa.gov Language: English - Date: 2014-12-04 01:13:30 Newborn screening Pediatrics Organic chemistry Tyrosinemia Tyrosine Association of Public Health Laboratories Tyr Health Chemistry Epidemiology
8	The National Organization for Rare Disorders NORD Guides for Physicians #1 Physician’s Guide to Add to Reading List Source URL: rarediseases.org Language: English - Date: 2012-12-18 11:57:21 Tyrosinemia Fumarylacetoacetate hydrolase Rare diseases Nitisinone Newborn screening Fanconi syndrome Jaundice Tyrosinemia type II Health Medicine Type I tyrosinemia
9	Microsoft Word - Tyrosinemia 2013.doc Add to Reading List Source URL: www.newbornscreening.info Language: English - Date: 2013-07-18 20:53:14 Aromatic amino acids Glucogenic amino acids Ketogenic amino acids Proteinogenic amino acids Tyrosinemia Type I tyrosinemia Newborn screening Nitisinone Fumarylacetoacetate hydrolase Health Chemistry Medicine
10	NEWBORN SCREENING FACT SHEET FAH Deficiency (Tyrosinemia Type[removed]) Add to Reading List Source URL: www.ndhealth.gov Language: English - Date: 2009-02-19 11:31:54 Tyrosinemia Type I tyrosinemia Newborn screening Phenylketonuria Nitisinone Rickets Fumarylacetoacetate hydrolase Liver transplantation Urea cycle disorder Medicine Health Hepatology