(Q68936935)

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Contribution of extrahepatic tissues to biochemical abnormalities in hereditary tyrosinemia type I: study of three patients after liver transplantation

scientific article published on 01 March 1987

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scholarly article

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28 September 2019

Contribution of extrahepatic tissues to biochemical abnormalities in hereditary tyrosinemia type I: study of three patients after liver transplantation (English)

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3546650%20AND%20SRC:MED&resulttype=core&format=json

28 September 2019

tyrosinemia type I

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based on heuristic

inferred from title

5

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N Ascher

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28 September 2019

Harvey L. Sharp

3

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H L Sharp

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28 September 2019

Deborah K. Freese

2

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D K Freese

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28 September 2019

author name string

M Tuchman

1

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28 September 2019

M L Ramnaraine

4

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28 September 2019

J R Bloomer

6

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1 March 1987

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28 September 2019

The Journal of Pediatrics

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28 September 2019

110

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28 September 2019

3

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28 September 2019

399-403

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28 September 2019

The occurrence of hepatoma in the chronic form of hereditary tyrosinemia

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https://api.crossref.org/works/10.1016%2FS0022-3476%2887%2980501-2

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2887%2980501-2

7 January 2021

Tyrosinosis. A study of 6 cases

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2887%2980501-2

7 January 2021

Excretion of δ-aminolevulinic acid in hereditary tyrosinemia

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2887%2980501-2

7 January 2021

Enzyme Defect in a Case of Tyrosinemia Type I, Acute Form

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2887%2980501-2

7 January 2021

Hereditary tyrosinemia and the heme biosynthetic pathway. Profound inhibition of delta-aminolevulinic acid dehydratase activity by succinylacetone

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2887%2980501-2

7 January 2021

Tyrosinemia with acute intermittent porphyria: aminolevulinic acid dehydratase deficiency related to elevated urinary aminolevulinic acid levels

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2887%2980501-2

7 January 2021

Persistent succinylacetone excretion after liver transplantation in a patient with hereditary tyrosinaemia type I

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2887%2980501-2

7 January 2021

Determination of urinary succinylacetone by capillary gas chromatography

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2887%2980501-2

7 January 2021

Detection of succinylacetone and the use of its measurement in mass screening for hereditary tyrosinemia

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2887%2980501-2

7 January 2021

Studies in lead poisoning. II. Correlation between the ratio of activated to inactivated delta-aminolevulinic acid dehydratase of whole blood and the blood lead level

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2887%2980501-2

7 January 2021

Hyperkalaemia in cyclosporin-treated renal allograft recipients

1 reference

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7 January 2021

Identifiers

10.1016/S0022-3476(87)80501-2

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28 September 2019

1 reference

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28 September 2019

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