Studies on phenylketonuria. I. Restricted phenylalanine intake in phenylketonuria.
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A different approach to treatment of phenylketonuria: phenylalanine degradation with recombinant phenylalanine ammonia lyaseA comparison of the phenylalanine content of the hemoglobin of normal and phenylketonuric individuals: determination by ion exchange chromatography.Diseases of phenylalanine metabolism.Phenylketonuria testing--its role in pediatrics and public health.Sapropterin dihydrochloride, 6-R-L-erythro-5,6,7,8-tetrahydrobiopterin, in the treatment of phenylketonuria.Genetic screening.Extensive restriction site polymorphism at the human phenylalanine hydroxylase locus and application in prenatal diagnosis of phenylketonuriaPhenylketonuria: a review.Evaluation of orally administered PEGylated phenylalanine ammonia lyase in mice for the treatment of Phenylketonuria.Diminished phenylketonuria in phenylpyruvic oligophrenia after administration of L-glutamine, L-glutamate or L-asparagine.The differential view of genotype-phenotype relationships.Case-finding in phenylketonuria: 3. One-way paper chromatography of amino acids in blood.The dietary treatment of phenylketonuria.Preclinical evaluation of multiple species of PEGylated recombinant phenylalanine ammonia lyase for the treatment of phenylketonuriaClinical therapeutics for phenylketonuria.A chemical investigation of the defects of myelination in phenylketonuria.Epinephrine metabolites and pigmentation in the central nervous system in a case of phenylpyruvic oligophrenia.The dietary treatment of inborn errors of metabolism.Birth weight and pathogenesis in phenylketonuria.Phenylalanine-restricted diets in the treatment of phenylketonuriaPhenylketonuria with normal intelligence and Gowers' muscular dystrophy.Studies in maple syrup urine disease.Human phenylalanine hydroxylase mutations and hyperphenylalaninemia phenotypes: a metanalysis of genotype-phenotype correlations.The contributions of Louis I Woolf to the treatment, early diagnosis and understanding of phenylketonuria.Strategies Used in Production of Phenylalanine-Free Foods for PKU Management
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P2860
Studies on phenylketonuria. I. Restricted phenylalanine intake in phenylketonuria.
description
1955 nî lūn-bûn
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1955 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
1955 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
1955年の論文
@ja
1955年論文
@yue
1955年論文
@zh-hant
1955年論文
@zh-hk
1955年論文
@zh-mo
1955年論文
@zh-tw
1955年论文
@wuu
name
Studies on phenylketonuria. I. Restricted phenylalanine intake in phenylketonuria.
@ast
Studies on phenylketonuria. I. Restricted phenylalanine intake in phenylketonuria.
@en
type
label
Studies on phenylketonuria. I. Restricted phenylalanine intake in phenylketonuria.
@ast
Studies on phenylketonuria. I. Restricted phenylalanine intake in phenylketonuria.
@en
prefLabel
Studies on phenylketonuria. I. Restricted phenylalanine intake in phenylketonuria.
@ast
Studies on phenylketonuria. I. Restricted phenylalanine intake in phenylketonuria.
@en
P2860
P356
P1476
Studies on phenylketonuria. I. Restricted phenylalanine intake in phenylketonuria.
@en
P2093
ARMSTRONG MD
P2860
P304
P356
10.1172/JCI103105
P407
P577
1955-04-01T00:00:00Z