An inborn defect in the metabolism of tyrosine in infants on a normal diet.
作者信息
Bloxam H R, Day M G, Gibbs N K, Woolf L I
机构信息
M.R.C. Population Genetics Research Unit, Old Road, Headington, Oxford, and the Public Health Department, City Hall, Cardiff.
出版信息
Biochem J. 1960 Nov;77(2):320-6. doi: 10.1042/bj0770320.
Abstract
摘要
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An inborn defect in the metabolism of tyrosine in infants on a normal diet.正常饮食的婴儿体内酪氨酸代谢的先天性缺陷。
Biochem J. 1960 Nov;77(2):320-6. doi: 10.1042/bj0770320.
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Pilot use of the early motor repertoire in infants with inborn errors of metabolism: outcomes in early and middle childhood.先天性代谢缺陷婴儿早期运动技能的初步应用：儿童早期和中期的结果
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[Acute metabolic liver in infants. Remarks on a practical approach].
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AN INBORN DEFECT OF INTESTINAL ABSORPTION OF CERTAIN MONOSACCHARIDES.某些单糖肠道吸收的先天性缺陷。
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引用本文的文献
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Studies on l-tyrosine O-sulphate. 1. Preparation and properties of potassium p-hydroxyphenylpyruvic acid [S]sulphate.L-酪氨酸O-硫酸盐的研究。1. 对羟基苯丙酮酸[S]硫酸盐钾的制备及性质
Biochem J. 1963 Jun;87(3):541-5. doi: 10.1042/bj0870541.
2
THE PLASMA TYROSINE LEVELS OF PREMATURE BABIES.早产儿的血浆酪氨酸水平。
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DIETARY TREATMENT OF A CHILD WITH MAPLE SYRUP URINE DISEASE (BRANCHED-CHAIN KETOACIDURIA).枫糖尿症（支链酮酸尿症）患儿的饮食治疗
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Effects of amino acid loads on a health infant with the biochemical features of Hartnup disease.氨基酸负荷对一名具有哈特纳普病生化特征的健康婴儿的影响。
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Tyrosinosis (inborn hepato-renal dysfunction).酪氨酸血症（先天性肝肾机能障碍）。
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Disorders of tyrosine metabolism.酪氨酸代谢紊乱。
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Protein intake and plasma amino-acids of infants of low birth weight.低出生体重儿的蛋白质摄入量与血浆氨基酸
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本文引用的文献
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THE CONTROL OF EXPERIMENTAL ALCAPTONURIA BY MEANS OF VITAMIN C.通过维生素C对实验性黑尿症的控制
Science. 1939 Dec 1;90(2344):517. doi: 10.1126/science.90.2344.517.
2
A DEFECT IN THE METABOLISM OF AROMATIC AMINO ACIDS IN PREMATURE INFANTS: THE ROLE OF VITAMIN C.早产儿芳香族氨基酸代谢缺陷：维生素C的作用。
Science. 1939 Dec 29;90(2348):620-1. doi: 10.1126/science.90.2348.620.
3
A new error of tyrosine metabolism: tyrosinosis. The intermediary metabolism of tyrosine and phenylalanine.酪氨酸代谢的一种新病症：酪氨酸血症。酪氨酸和苯丙氨酸的中间代谢。
Biochem J. 1932;26(4):917-40. doi: 10.1042/bj0260917.
4
THE METABOLISM OF l-TYROSINE IN INFANTILE SCURVY.婴儿坏血病中L-酪氨酸的代谢
J Clin Invest. 1950 Mar;29(3):325-35. doi: 10.1172/JCI102261.
5
A DEFECT IN THE METABOLISM OF TYROSINE AND PHENYLALANINE IN PREMATURE INFANTS. III. DEMONSTRATION OF THE IRREVERSIBLE CONVERSION OF PHENYLALANINE TO TYROSINE IN THE HUMAN ORGANISM.早产儿酪氨酸和苯丙氨酸代谢的缺陷。III. 人体内苯丙氨酸向酪氨酸不可逆转化的证明。
J Clin Invest. 1943 Jul;22(4):551-62. doi: 10.1172/JCI101426.
6
A DEFECT IN THE METABOLISM OF TYROSINE AND PHENYLALANINE IN PREMATURE INFANTS. II. SPONTANEOUS OCCURRENCE AND ERADICATION BY VITAMIN C.早产儿酪氨酸和苯丙氨酸代谢缺陷。II. 维生素C的自然发生和消除作用
J Clin Invest. 1941 Mar;20(2):209-19. doi: 10.1172/JCI101213.
7
A DEFECT IN THE METABOLISM OF TYROSINE AND PHENYLALANINE IN PREMATURE INFANTS. I. IDENTIFICATION AND ASSAY OF INTERMEDIARY PRODUCTS.早产儿酪氨酸和苯丙氨酸代谢缺陷。I. 中间产物的鉴定与测定
J Clin Invest. 1941 Mar;20(2):199-207. doi: 10.1172/JCI101212.
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Estimation of phenylpyruvic acid.
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The oxidation in liver of l-tyrosine to acetoacetate through p-hydroxyphenylpyruvate and homogentisic acid.L-酪氨酸在肝脏中通过对羟基苯丙酮酸和尿黑酸氧化生成乙酰乙酸。
Biochem J. 1951 Oct;49(5):686-93. doi: 10.1042/bj0490686.
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