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Type I tyrosinemia
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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	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
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: 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
5	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
6	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
7	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
8	Overview of Newborn Screening for Tyrosinemia – For Parents What is newborn screening? What are the symptoms of tyrosinemia? Before babies go home from the nursery, they Add to Reading List Source URL: www.in.gov Language: English - Date: 2014-10-23 17:39:47 Chemistry Fumarylacetoacetate hydrolase Newborn screening Tyrosine Type I tyrosinemia Tyrosinemia type III Health Tyrosinemia Medicine
9	Tyrosinemia Type I (TYR) 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 Add to Reading List Source URL: www.michigan.gov Language: English - Date: 2012-12-07 20:49:08 Newborn screening Screening Tyrosine Type I tyrosinemia Tyrosinemia type III Health Medicine Tyrosinemia
10	Tyrosinemia Type II and III (TYR II/TYR III) 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, h Add to Reading List Source URL: www.michigan.gov Language: English - Date: 2012-12-07 10:37:04 Palmoplantar keratodermas Newborn screening Tyrosine Screening Type I tyrosinemia Health Medicine Tyrosinemia

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