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Tetrahydrobiopterin deficiency
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1	PDF Document Add to Reading List Source URL: www.pbs.gov.au Language: English - Date: 2014-10-01 21:56:22 Coenzymes Pteridines Alcohols Lactams Tetrahydrobiopterin Phenylketonuria 6-Pyruvoyltetrahydropterin synthase deficiency Phenylalanine hydroxylase Pharmaceutical Benefits Scheme Medicine Health Chemistry
2	Phenylketonuria (PKU) What is Phenylketonuria? Phenylketonuria (also known as PKU) is an inherited condition that affects the way a person’s body uses protein. A person with PKU cannot use a component of protein called Add to Reading List Source URL: health.state.tn.us Language: English - Date: 2007-05-01 15:48:27 Mental retardation Phenylketonuria PKU Phenylalanine Dominance Hyperphenylalanemia Medical genetics Newborn screening Tetrahydrobiopterin deficiency Medicine Health Biology
3	Phenylketonuria (PKU) Phenylketonuria is an inherited autosomal recessive disorder of phenylalanine metabolism. PKU is usually detected within the first few days of life by newborn screening. It is characterized by the a Add to Reading List Source URL: www.maine.gov Language: English - Date: 2011-11-10 05:39:05 Medicine Biology Pediatrics PKU Phenylalanine Newborn screening Dominance Tetrahydrobiopterin deficiency Hyperphenylalanemia Health Mental retardation Phenylketonuria
4	Phenylketonuria (PKU) (metabolic condition: amino acid disorder) Also known as: • phenylalanine hydroxylase deficiency Add to Reading List Source URL: www.albertahealthservices.ca Language: English - Date: 2013-09-16 18:35:23 Mental retardation Phenylketonuria Coenzymes Pteridines Tetrahydrobiopterin PKU Medical genetics Phenylalanine hydroxylase Phenylalanine Medicine Health Chemistry
5	Diagnosis: Tetrahydrobiopterin Deficiency (BH4) Diagnosis: Tetrahydrobiopterin Deficiency (BH4) BH4 is an inherited disorder that increases the blood levels off phenylalanine, an amino acid obtained through the diet. It Add to Reading List Source URL: www.wadsworth.org - Date: 2009-07-15 13:48:22
6	Phenylketonuria (PKU) What is Phenylketonuria? Phenylketonuria (also known as PKU) is an inherited condition that affects the way a person’s body uses protein. A person with PKU cannot use a component of protein called Add to Reading List Source URL: health.tn.gov Language: English - Date: 2007-05-01 15:48:27 Mental retardation Phenylketonuria PKU Phenylalanine Dominance Hyperphenylalanemia Medical genetics Newborn screening Tetrahydrobiopterin deficiency Medicine Health Biology
7	Climb National Information Centre for Metabolic Diseases Tetrahydrobiopterin Deficiency - General • • Add to Reading List Source URL: www.climb.org.uk Language: English - Date: 2014-03-19 09:33:49 Pteridines Organic chemistry Mental retardation Phenylketonuria Tetrahydrobiopterin PKU Biopterin Phenylalanine Disease Chemistry Health Coenzymes
8	Parent Fact Sheet Phenylketonuria (PKU) (Fee nul key tone your ee a) What is PKU? Phenylketonuria (PKU) is a metabolic disorder. This means the body has a chemical imbalance. PKU is Add to Reading List Source URL: www.vdh.virginia.gov Language: English - Date: 2014-04-08 11:13:09 Medicine Genetic genealogy Newborn screening PKU Phenylalanine Hyperphenylalanemia Tetrahydrobiopterin deficiency Health Mental retardation Phenylketonuria
9	Phenylketonuria (PKU) What is Phenylketonuria? Phenylketonuria (also known as PKU) is an inherited condition that affects the way a person’s body uses protein. A person with PKU cannot use a component of protein called Add to Reading List Source URL: health.state.tn.us Language: English - Date: 2007-05-01 15:48:27 Mental retardation Phenylketonuria PKU Phenylalanine Dominance Hyperphenylalanemia Medical genetics Newborn screening Tetrahydrobiopterin deficiency Medicine Health Biology
10	Visio-Phenylalanine[removed] no edits.vsd Add to Reading List Source URL: www.ncbi.nlm.nih.gov Language: English Tetrahydrobiopterin deficiency Phenylketonuria Phenylalanine hydroxylase Tetrahydrobiopterin Phenylalanine PKU Medical genetics Newborn screening Neurotransmitter Medicine Health Chemistry