(Q35502573)

8 August 2017

1 reference

title

INHERITED METABOLIC DISORDERS: ERRORS OF PHENYLALANINE AND TYROSINE METABOLISM. (English)

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8 August 2017

WOOLF LI

1

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PubMed ID

14281820

8 August 2017

language of work or name

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1 January 1963

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Advances in Clinical Chemistry

8 August 2017

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8 August 2017

6

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8 August 2017

97-230

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Serum vitamin B12 concentrations in megaloblastic anemia associated with kwashiorkor and marasmus

8 August 2017

1 reference

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7 January 2021

Protection afforded by sickle-cell trait against subtertian malareal infection

1 reference

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7 January 2021

Genetic factors in resistance to malaria.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Identification of heterozygotes with phenylketonuria on basis of blood tyrosine responses

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Studies on phenylketonuria. V. Observations on a newborn infant with phenylketonuria

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Phenylketonuria VIII. Relation between age, serum phenylalanine level, and phenylpyruvic acid excretion

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

On the excretion of indole derivatives in phenylketonuria.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Studies on phenylketonuria. I. Restricted phenylalanine intake in phenylketonuria

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Studies on phenylketonuria. IX. Further observations on the effect of phenylalanine-restricted diet on patients with phenylketonuria

1 reference

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7 January 2021

3-Methoxy-4-hydroxy-D-mandelic acid, a urinary metabolite of norepinephrine

1 reference

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7 January 2021

Endogenous formation of hippuric acid

1 reference

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7 January 2021

O-Methylation of Epinephrine and Other Catechols in vitro and in vivo

1 reference

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7 January 2021

3-Methoxy-4-hydroxyphenylglycol sulfate, a new metabolite of epinephrine and norepinephrine

1 reference

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7 January 2021

A case of congenital cirrhosis of the liver with renal tubular defects akin to those in the Fanconi syndrome

1 reference

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7 January 2021

The relation of the pigment trichosiderin to hair colour

1 reference

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7 January 2021

The Pigment, Trichosiderin, from Human Red Hair

1 reference

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7 January 2021

The electron microscopy of human hair pigments

1 reference

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7 January 2021

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

1 reference

7 January 2021

The nitration of benzoic and phenylacetic acids and phenylalanine; the chemical basis of the Mohler and Kapeller-Adler reactions

1 reference

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7 January 2021

Iris colour in phenylketonuria

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Paper chromatographic method for estimation of phenylalanine.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Simple method for detection of phenylketonuria

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Estimation of Phenylpyruvic Acid

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Pathways of iodine metabolism

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Influence of phenylalanine intake on phenylketonuria

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Pigment spread and cell heredity in guinea-pigs' skin

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

An inborn defect in the metabolism of tyrosine in infants on a normal diet

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Dehydroxylation of Caffeic Acid by Rat and Rabbit Cæcal Contents and Sheep Rumen Liquor

1 reference

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7 January 2021

Effects of l-phenylalanine and sodium phenylpyruvate on the formation of adrenaline from l-tyrosine in adrenal medulla in vitro

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Dietary and Biochemical Control of Phenylketonuria

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

The birthplaces of parents and grandparents of a series of patients with phenylketonuria in in south-east England

1 reference

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7 January 2021

A note on the future of phenylketonuria

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7 January 2021

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

1 reference

7 January 2021

Phenylketonuria. II. Results of treatment of infants and young children. A report of 10 cases

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Phenylketonuria with normal intelligence and Gowers' muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Phenylpyruvic oligophrenia in a Jewish child

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Phenylalanine hydroxylase activity in dilute and nondilute strains of mice

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Urinary excretion of 3,4-dihydroxyphenylalanine (DOPA) in two children of short stature with malnutrition

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Phenylpyruvic oligophrenia

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

An atypical case of phenylketonuria

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Dilution of hair colour in phenylketonuria

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

[Isolation in a crystalline form and identification of p-cresol sulfate in pregnancy urine]

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

The association of phenylketonuria with leucodystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

A chemical investigation of the defects of myelination in phenylketonuria

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

o-Hydroxyphenylacetic acid excretion in the phenylalanine tolerance test for carriers of phenylketonuria

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Nonspecific formation of hydroxylated metabolites of the aromatic amino acids

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Inhibition of 5-Hydroxytryptophan Decarboxylase by Phenylalanine Metabolites

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

The metabolism of aromatic aminoacids in kwashiorkor

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Studies on sulphatases. 23. The enzymic desulphation of tyrosine O-sulphate

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Tyrosine Metabolism in Melanoma

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Ketogenesis-antiketogenesis: Ketogenesis from amino-acids

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Problems of routine screening for phenylketonuria

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

1 reference

7 January 2021

Inhibition of DOPA decarboxylase by aromatic acids associated with phenylpyruvic oligophrenia.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Epinephrine metabolites and pigmentation in the central nervous system in a case of phenylpyruvic oligophrenia

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Isolation of Melanin Granules

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

A histochemical autoradiographic method for demonstration of tyrosinase in human melanocytes, nevi and malignant melanoma

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Tyrosinase in human skin: demonstration of its presence and of its role in human melanin formation

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

The electroencephalogram in phenylpyruvic oligophrenia.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

On the nature of pigment granules in the cells of the locus coeruleus and substantia nigra.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Über Ausscheidung von Phenylbrenztraubensäure in den Harn als Stoffwechselanomalie in Verbindung mit Imbezillität

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

The effect of aromatic amino acids on the hydroxylation of tryptophan

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Albinism in Northern Ireland

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Effect of citrovorum factor upon tyrosine metabolism in clinical scurvy

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Alcaptonuria and ochronosis; with a report of three patients and metabolic studies in two

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

The production of amines by bacteria: The production of tyramine by Streptococcus faecalis

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

The incidence of alkaptonuria: a study in chemical individuality. 1902 [classical article]

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Tests for phenylketonuria: results of a one-year programme for its detection in infancy and among mental defectives.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Studies on phenylketonuria. II. The excretion of N-acetyl-L-phenylalanine in phenylketonuria

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Phenylalanine metabolism and folic acid antagonists

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Developmental changes of p-hydroxyphenylpyruvate-oxidase activity in mammalian liver.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

The Effect of Pteroylglutamic Acid on the Aromatic Amino Acid Metabolism of Premature Infants

1 reference

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7 January 2021

Catecholamine metabolism in a functional neural tumor

1 reference

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7 January 2021

[Contribution to the etiology of ochronosis in alkaptonuria]

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Formation of Hippuric Acid from Phenylalanine labelled with Carbon-14 in Phenylketonuric Subjects

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Phenylpyruvic oligophrenia; an evaluation of the light-sensitive and pigmentary characteristics of seventeen patients

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Effect of a phenylalanine-restricted diet on patients with phenylketonuria; clinical observations in three cases.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Phenylketonuria treated from earliest infancy; report of three cases

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Termination of Dietary Treatment of Phenylketonuria

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Detection of the heterozygous carriers of phenylketonuria

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Serum phenylalanine and tyrosine levels in the newborn infant

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Some investigations on the metabolism of phenylalanine and tyrosine in children with vitamin C deficiency

1 reference

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7 January 2021

Genetic regulatory mechanisms in the synthesis of proteins

1 reference

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7 January 2021

Nonspecificity of tyrosine transaminase: An explanation for the simultaneous induction of tyrosine, phenylalanine, and tryptophan transaminase activities in rat liver

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Excretion of phenylalanine and derivatives in phenylpyruvic oligophrenia

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Studies on phenylpyruvic oligophrenia; phenylpyruvic acid content on blood.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Detection of heterozygotes for phenylketonuria

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

The participation of tetra-hydrofolic acid in the enzymic conversion of phenylalanine to tyrosine

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Phenylalanine hydroxylation cofactor in phenylketonuria

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Hepatic metabolism of phenylalanine during development

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Development of phenylalanine hydroxylase in mammalian liver

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Alkaptonuria; report of a family with seven cases appearing in four successive generations, with metabolic studies in one patient

1 reference

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7 January 2021

Excretion of rho-oxyphenylacetic acid after administration rho-oxyphenylpyruvic acid in the guinea pig

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Metabolism of dl-adrenaline-2-C14 in the human

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

The oxidation in liver of l-tyrosine to acetoacetate through p-hydroxyphenylpyruvate and homogentisic acid

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Certain aspects of tyrosine metabolism in the young. II. The tyrosine oxidizing system of fetal rat liver

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Certain aspects of tyrosine metabolism in the young. I. The development of the tyrosine oxidizing system in human liver

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Presence of Metanephrine and Normetanephrine in Normal Human Urine

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Ascorbic acid and the oxidation of tyrosine

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

A Requirement for Catalase in Tyrosine Metabolism : the Oxidation of p-Hydroxy-phenylpyruvic Acid to Homogentisic Acid

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

The role of ascorbic acid in tyrosine metabolism

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Solubility of Melanins

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Estimation of the amount of pigment present in human hair

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

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.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

A DEFECT IN THE METABOLISM OF TYROSINE AND PHENYLALANINE IN PREMATURE INFANTS. II. SPONTANEOUS OCCURRENCE AND ERADICATION BY VITAMIN C.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

A DEFECT IN THE METABOLISM OF AROMATIC AMINO ACIDS IN PREMATURE INFANTS: THE ROLE OF VITAMIN C

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

A DEFECT IN THE METABOLISM OF TYROSINE AND PHENYLALANINE IN PREMATURE INFANTS. I. IDENTIFICATION AND ASSAY OF INTERMEDIARY PRODUCTS.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Effect of ACTH and some adrenocortical steroids on the metabolism of tyrosine and phenylalanine in premature infants.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Role of enzymatic adaptation in production of experimental alkaptonuria

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Studies on phenylketonuria. VI. EEG studies in phenylketonuria.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Maple syrup urine disease; an inborn error of the metabolism of valine, leucine, and isoleucine associated with gross mental deficiency.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Structures and functions of the phenolase complex.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

OXYGEN TRANSFER AND ELECTRON TRANSPORT BY THE PHENOLASE COMPLEX1

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

A Mehanism of the Indole Defect in Experimental Phenylketonuria.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

A new error of tyrosine metabolism: tyrosinosis. The intermediary metabolism of tyrosine and phenylalanine

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Studies on partially purified phenylalanine hydroxylase.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

On the nature of enzymatic defect in phenylpyruvic oligophrenia.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Enzymatic hydroxylation of aromatic compounds

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Competitive inhibition of mammalian tyrosinase by phenylalanine and its relationship to hair pigmentation in phenylketonuria.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

THE METABOLISM OF l-TYROSINE IN INFANTILE SCURVY.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Phenylketonuria; data on 47 British families

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Phenylketonuria treated from early infancy

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Studies on alcaptonuria: 1. The estimation of homogentisic acid

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Studies in alcaptonuria: 3. Experimental alcaptonuria in rats

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Studies on alcaptonuria: 2. Investigations on a case of human alcaptonuria

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Evaluation of familial biochemically determined mental retardation in children, with special reference to aminoaciduria.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

The influence of l-ascorbic acid on the rupture of the benzene ring of l-tyrosine consumed in high doses by guinea-pigs

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

5-Hydroxytryptamine deficiency in phenylketonuria.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Decreased 5-hydroxytryptophan decarboxylase activity in phenylketonuria

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

The Relationship between Decreased 5-Hydroxyindole Metabolism and Mental Defect in Phenylketonuria

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

A modified procedure for the automatic analysis of amino acids

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Oxidation of Phenylpyruvates to Aromatic Aldehydes and Oxalate

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Neuro-pathologic observations in phenylketonuria.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Enzymic hydroxylation of aromatic compounds. II. Further studies of the properties of the microsomal hydroxylating system

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Studies on l-tyrosine O-sulphate. 2. Identification of p-hydroxyphenylpyruvic acid [S]sulphate as a metabolite of l-tyrosine O[S]-sulphate in the rat.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Development of phenylalanine hydroxylase in liver of the rat

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Conversion of tryptophan to 5-hydroxytryptophan by phenylalanine hydroxylase

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Nature, biosynthesis and metabolism of thyroid hormones

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Inhibitory-action of human epidermis on melanin formation

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Megaloblastic Anaemia Complicating Dietary Treatment of Phenylketonuria in Infancy

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Phenylalanine metabolism in control subjects, mental patients, and phenylketonurics.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

The effect of folinic acid (citrovorum factor) and of cortisone on the metabolism of tyrosine in the scorbutic monkey

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Distribution of catechol compounds in human brain

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

The interconversion of amino acids after their incorporation into haemoglobin and myosin

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Comparison of serum phenylalanine levels with growth in Guthrie's inhibition assay in newborn infants

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

[Urinary excretion of indole-pyroracemic acid in normal conditions and in Fölling's disease]

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

THE CONTROL OF EXPERIMENTAL ALCAPTONURIA BY MEANS OF VITAMIN C

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Skin cancer in the South African Bantu

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Exogenous Sources of Urinary Phenol and Indole Acids

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

An inborn error of metabolism with the urinary excretion of alpha-hydroxy-butyric acid and phenylpyruvic acid

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

The Phenylalanine Requirement of the Normal Infant

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Phenylpyruvic oligophrenia in a mulatto; probable manifestation of the pleiotropic effect.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Sporadic or non-endemic familial cretinism with goiter.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Ultra-violet Absorption Investigation of Melanins

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Further notes on albinism among the san blas Cuna, Panama

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Phenylpyruvic acid as a possible precursor of o-hydroxyphenylacetic acid in man

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Effect of phenylalanine metabolites on urinary excretion of indole-3-acetic acid and 5-hydroxyindole-3-acetic acid in man

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

The Vitamin C content of the liver of newborn infants

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Marriage of two complete albinos with normally pigmented offspring

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

The renal clearance of phenylpyruvate

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Occurrence, isolation and identification of 3-methoxy-4-hydroxyphenylalanine

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

X-chromosomal ocular albinism in a Dutch family

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Studies on conversion of phenylalanine to tyrosine in phenylpyruvic oligophrenia.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Metabolites of Phenylalanine in the Urine of Children with Kwashiorkor

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Significance and rearrangements of quinol models of tyrosine metabolites

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

1 reference

7 January 2021

Nutrition in relation to phenylketonuria

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

The metabolism of tyrosine and phenylalanine in premature infants; the effect of large doses

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

The urinary excretion of amino acids and sugars in early infancy

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Phenylketonuria with a study of the effect upon it of glutamic acid

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Treatment of phenylketonuria with a diet low in phenylalanine.

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

The dietary treatment of phenylketonuria

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

Atypical phenylketonuria in sisters with normal offspring

1 reference

https://api.crossref.org/works/10.1016%2FS0065-2423%2808%2960239-5

7 January 2021

10.1016/S0065-2423(08)60239-5

Identifiers

DOI

0 references

PubMed ID

14281820

1 reference

PubMed ID

14281820