phenylketonuria (Also phenylketonurias) : Related Words Words similar in meaning to phenylketonuria
- phenylketonuria«
- phenylalanine«
- pku«
- phe«
- inborn error of metabolism«
- metabolize«
- metabolic«
- tyrosine«
- liver«
- diet«
- enzyme«
- blood phe level«
- disorder«
- pah«
- amino acid«
- urine«
- disease«
- lnaas«
- -uria«
- tetrahydrobiopterin«
- free amino acid«
- intellectual disability«
- enzyme phenylalanine hydroxylase«
- amino acid phenylalanine«
- classical pku«
- birth«
- classic pku«
- pah gene«
- phenylalanine level«
- hyperphenylalaninemia«
- brain«
- pregnancy«
- tyr«
- treatment«
- level«
- gene«
- cofactor«
- newborn screening«
- carrier«
- widespread newborn screening«
- protein substitute«
- pku diet«
- phenylketones«
- phenylketone«
- phe level«
- mild hyperphenylalaninemia«
- low phe level«
- hyperphe«
- dopa«
- patient«
- symptom«
- pah enzyme«
- pah activity«
- blood«
- tetrahydrobiopterin deficiency«
- seizure«
- regular blood test«
- % chance«
- phenylacetate«
- følling«
- dopamine«
- child«
- blood test«
- baby«
- phenylpyruvate«
- pku.«
- odor«
- amino acid tyrosine«
- people«
- protein«
- deficiency«
- target range«
- food«
- mother«
- microcephaly«
- amount«
- toxic level«
- catabolism«
- mood disorder«
- eczema«
- tryptophan«
- damage«
- infant«
- gene therapy«
- elevated level«
- dag«
- substance«
- peg«
- physician«
- varied detection technique«
- variant pku«
- untreated pku«
- untreated infant«
- united state caucasian«
- transaminase pathway«
- toxic amyloid«
- their pku«
- tetrahydrobiopterin form«
- specialist metabolic dietitian«
- single pku allele«
- recombinant phenylalanine ammonia lyase«
- pure form cgmp«
- protein substitute formula«
- plasma phe level«
- pku mutation«
- pku mother«
- pku gene«
- photometric detection«
- phenylalanine diet«
- phe buildup«
- people pku«
- pah mutation«
- pah deficiency«
- optimal brain development«
- nutritional information label«
- norwegian physician ivar asbjørn følling«
- normal pah activity«
- normal infant feeding«
- neutral amino acids(lnaas«
- mild pku«
- mild hpa«
- maternal blood phe level«
- many untreated pku patient«
- many pku patient«
- low phenylalanine level«
- lnaat«
- irregular motor functioning«
- hyperphenylalanemia«
- hpabh4d.«
- hpabh4c«
- hpabh4b«
- hpabh4a«
- his careful science«
- his careful analysis«
- hepatic enzyme phenylalanine hydroxylase«
- fungal toxin ochratoxin a.«
- functional pah enzyme«
- excessive phenylalanine«
- enzyme pah«
- dihydrobiopterin reductase activity«
- dihydrobiopterin involvement«
- dietary phenylalanine«
- dietary phe intake«
- dependent living homes/institutions«
- deficient hyperphenylalaninemia«
- deficient dihydrobiopterin reductase«
- daily phe intake«
- common amino acid metabolic«
- classical pku.«
- classic pku.«
- classic phenylketonuria«
- casein glycomacropeptide«
- brain function abnormality«
- beneficial nutritional effect«
- autosomal recessive metabolic genetic disorder«
- autosomal recessive meaning«
- amino acid measurement«
- allelic genetic heterogeneity«
- reaction«
- fetus«
- pal«
- special diet low«
- routine newborn screening test«
- prescription formula«
- pku allele«
- periodic blood test«
- lowfat cottage cheese«
- lofenalac«
- fluorometric«
- enzyme substitution therapy«
- borgny egeland«
- analogous enzyme«
- oxidation«
- metabolism«
- benefit«
- white matter development«
- severe accumulation«
- relevant mutation«
- pku patient«
- optimal health range«
- neurocognitive«
- milk peptide«
- hair coloration«
- excess phenylpyruvic acid«
- dopamine lead«
- body«
- sweetener aspartame«
- quinonoid«
- newborn screening panel«
- lnaa«
- extensive inbreeding«
- nutrient«
- low level«
- untreated child«
- specific carrier protein«
- defect«
- protein retention«
- normal bread«
- neonatal heel prick«
- bacterial inhibition assay«
- repeat test«
- progressive impairment«
- phenylpyruvic acid«
- insufficient diet«
- detailed chemical analysis«
- cofactor tetrahydrobiopterin«
- mutation«
- essential compound«
- amyloid disease«
- neurotransmitter synthesis«
- ivar asbjørn følling«
- improved compliance«
- guthrie test«
- severe learning disability«
- newborn screening test«
- biopterin«
- author pearl s. buck«
- medication«
- proper activity«
- food diary«
- intrauterine environment«
- dihydrobiopterin«
- other therapy«
- eeg abnormality«
- neutral amino acid transporter«
- most baby«
- compound heterozygous mutation«
- biomarin«
- life«
- musty smell«
- enzyme tyrosine hydroxylase«
- normal life span«
- musty odor«
- neutral amino acid«
- further testing«
- dietary treatment«
- phenylalanine hydroxylase«
- typical diet«
- robert guthrie«
- normal brain development«
- dihydrochloride«
- bone pathology«
- µmol/l«
- protein catabolism«
- cerebral function«
- newborn screening program«
- safe range«
- diet food«
- insufficient level«
- supplements«
- medical food«
- white matter tract«
- many fruit«
- normal brain function«
- normal health«
- ratio«
- affected patient«
- dietary supplementation«
- many adult«
- special formula«
- clinical disorder«
- severe intellectual disability«
- rarer form«
- minor route«
- woman«
- starchy food«
- prolactin level«
- absorption rate«
- developmental milestone«
- enzyme function«
- diet low«
- amino acid metabolism«
- infant development«
- rom population«
- hypopigmentation«
- child who«
- spirulina«
- painstaking research«
- breastmilk«
- lighter skin«
- tandem mass spectrometry«
- affected child«
- chicken breast«
- permanent effect«
- screening«
- quantity«
- growth retardation«
- skin«
- treatment strategy«
- different people«
- myelination«
- macaque monkey«
- intestinal mucosa«
- excessive level«
- immunoassay«
- rikshospitalet«
- fair hair«
- strict diet«
- satiety«
- dietary intake«
- special supplement«
- blood brain barrier«
- additional complication«
- sufficient level«
- aspartame«
- strong smell«
- light skin«
- inborn error«
- grew«
- benzaldehyde«
- study«
- tentative evidence«
- benzoic acid«
- heterozygote«
- essential amino acid«
- prolactin«
- autosomal recessive disorder«
- congenital heart disease«
- motor cortex«
- phenyl«
- phenethylamine«
- physical symptom«
- coenzyme«
- watercress«
- gray matter«
- severe disability«
- low birth weight«
- benzene ring«
- algernon«
- clinical development«
- pronunciation«
- blood level«
- anecdotal report«
- initial test«
- protein content«
- oral administration«
- hyperactivity«
- urine sample«
- educational achievement«
- galactosemia«
- lysinemia«
- PKU«
- PAH«
- Niemann-Pick disease«
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