Hereditary tyrosinemia: Metabolic studies in a patient with partial p-hydroxyphenylpyruvate hydroxylase activity (Q70373185)

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10 October 2019

title

Hereditary tyrosinemia: metabolic studies in a patient with partial p-hydroxyphenylpyruvate hydroxylase activity (English)

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10 October 2019

Hereditary tyrosinemia: Metabolic studies in a patient with partial p-hydroxyphenylpyruvate hydroxylase activity (English)

1 reference

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29 March 2023

author name string

R. Jagenburg

1

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29 March 2023

B. Landblad

2

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29 March 2023

J. M. De Maré

3

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29 March 2023

S. Rödjer

4

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29 March 2023

language of work or name

English

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publication date

1 June 1972

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full work available at URL

10 October 2019

https://api.elsevier.com/content/article/PII:S0022347672800131?httpAccept=text/xml

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29 March 2023

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The Journal of Pediatrics

29 March 2023

published in

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10 October 2019

volume

80

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10 October 2019

issue

6

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10 October 2019

page(s)

994-1004

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10 October 2019

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Dietary treatment in tyrosinemia (tyrosinosis). With a note on the possible recognition of the carrier state

7 January 2021

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Excretion of δ-aminolevulinic acid in hereditary tyrosinemia

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STUDIES ON TYROSINOSIS: 1, EFFECT OF LOW-TYROSINE AND LOW-PHENYLALANINE DIET

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Dietary treatment of infantile tyrosinemia

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Recovery after dietary treatment of an infant with features of tyrosinosis

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[The catecholamines adrenalin and noradrenalin in the urine of the child]

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

7 January 2021

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The estimation of catechol amines in urine

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Radiochemical assays for p-hydroxyphenylpyruvate hydroxylase activity in human liver

7 January 2021

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Phenylalanine Absorption and Metabolism in Parkinsonian Patients

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STUDIES ON TYROSINOSIS: 2, ACTIVITY OF THE TRANSAMINASE, PARAHYDROXY-PHENYL-PYRUVATE OXIDASE, AND HOMOGENTISIC-ACID OXIDASE

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Enzymatic studies in a case of hereditary tyrosinemia with hepatoma

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Delayed maturation of tyrosine metabolism in a full-term sibling of a child with phenylketonuria.

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The urinary excretion of free amino acids and other amino compounds by the human

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Tyrosine Hydroxylase

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Developmental retardation associated with an abnormality in tyrosine metabolism. Report of a case

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29 March 2023

Identifiers

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5026040%20AND%20SRC:MED&resulttype=core&format=json

10 October 2019

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