An inborn defect in the metabolism of tyrosine in infants on a normal diet.
about
Genetic aspects of tyrosinemia in the Chicoutimi regionPhenylketonuria testing--its role in pediatrics and public health.Urinary phenolic acid and alcohol excretion in the newbornDIETARY TREATMENT OF A CHILD WITH MAPLE SYRUP URINE DISEASE (BRANCHED-CHAIN KETOACIDURIA).THE PLASMA TYROSINE LEVELS OF PREMATURE BABIES.Effects of amino acid loads on a health infant with the biochemical features of Hartnup disease.Diagnosis and treatment of tyrosinosisInsight on the impacts of free amino acids and their metabolites on the immune system from a perspective of inborn errors of amino acid metabolism.Studies on l-tyrosine O-sulphate. 1. Preparation and properties of potassium p-hydroxyphenylpyruvic acid [S]sulphateTyrosinosis (inborn hepato-renal dysfunction).Studies on L-tyrosine O-sulphate. 3. The metabolic fate of the L-tyrosine O[35S]-sulphate residue of 35S-labelled rabbit fibrinopeptide B.Reduction of aromatic alpha-keto acids by lactic dehydrogenase isozymes and aromatic alpha-keto acid reductase.Screening for inherited metabolic disease by plasma chromatography (Scriver) in a large city.Protein intake and plasma amino-acids of infants of low birth weight.Tyrosyluria in Human Subjects
P2860
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P2860
An inborn defect in the metabolism of tyrosine in infants on a normal diet.
description
1960 nî lūn-bûn
@nan
1960年の論文
@ja
1960年論文
@yue
1960年論文
@zh-hant
1960年論文
@zh-hk
1960年論文
@zh-mo
1960年論文
@zh-tw
1960年论文
@wuu
1960年论文
@zh
1960年论文
@zh-cn
name
An inborn defect in the metabolism of tyrosine in infants on a normal diet.
@en
type
label
An inborn defect in the metabolism of tyrosine in infants on a normal diet.
@en
prefLabel
An inborn defect in the metabolism of tyrosine in infants on a normal diet.
@en
P2093
P2860
P356
P1433
P1476
An inborn defect in the metabolism of tyrosine in infants on a normal diet.
@en
P2093
P2860
P304
P356
10.1042/BJ0770320
P407
P577
1960-11-01T00:00:00Z