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Inborn error of metabolism
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11	Microsoft Word - MSAC 1114 UMP Summary_circ090109.doc Add to Reading List Source URL: www.msac.gov.au Language: English - Date: 2014-08-07 23:58:26 Biology Mood disorders Pediatrics Inborn error of metabolism Metabolism
12	Supporting Information Lee et al[removed]pnas[removed]SI Text Datasets. The KEGG database (1) is a depository of the list of all metabolic reactions identified in a generic human cell, together with Add to Reading List Source URL: www.barabasilab.com Language: English - Date: 2008-07-22 16:39:08 Systems biology Bioinformatics Medical genetics Comorbidity Metabolic pathway Flux balance analysis KEGG Metabolic network Inborn error of metabolism Biology Metabolism Science
13	Application for Australian Government financial assistance for individuals with Inborn Error of Metabolism DHPR, Hyperphenylalaninemia and PKU Conditions Only Details of the person making the grant application (responsi Add to Reading List Source URL: health.gov.au Language: English* - Date: 2015-04-13 10:32:51 Phenylketonuria Medical informatics Health informatics Medicine Health Mental retardation
14	Statement of Principles concerning ALKAPTONURIA No. 47 of 2007 for the purposes of the Add to Reading List Source URL: www.rma.gov.au Language: English - Date: 2014-05-06 01:36:09 Alkaptonuria Homogentisic acid Homogentisate 1 2-dioxygenase Tyrosine International Statistical Classification of Diseases and Related Health Problems Inborn error of metabolism ICD-10 Medicine Health Chemistry
15	HK J Paediatr (new series) 2004;9:[removed]INDEX Volume[removed]New Series Add to Reading List Source URL: www.fmshk.com.hk Language: English - Date: 2006-06-28 04:24:00 Pediatric endocrinology Kidney transplantation Specialty Dialysis Renal replacement therapy Inborn error of metabolism Chronic kidney disease Kidney Medicine Nephrology Endocrinology
16	Application for Australian Government financial assistance for individuals with Inborn Error of Metabolism DHPR, Hyperphenylalaninemia and PKU Conditions Only Details of the person making the grant application (responsi Add to Reading List Source URL: www.health.gov.au Language: English* - Date: 2015-03-17 09:15:53 Phenylketonuria Medical informatics Health informatics Medicine Health Mental retardation
17	Statement of Principles concerning ALKAPTONURIA No. 48 of 2007 for the purposes of the Add to Reading List Source URL: www.rma.gov.au Language: English - Date: 2014-05-06 01:36:09 Alkaptonuria Homogentisic acid Homogentisate 1 2-dioxygenase Tyrosine International Statistical Classification of Diseases and Related Health Problems Inborn error of metabolism ICD-10 Medicine Health Chemistry
18	Activities in the field of rare diseases in Slovakia CISARIK František Faculty Hospital Žilina Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2014-12-08 11:13:50 Newborn screening Cystic fibrosis Congenital adrenal hyperplasia Inborn error of metabolism Congenital hypothyroidism Congenital disorder Health Pediatrics Medicine
19	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
20	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

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