(Q69382875)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2581063%20AND%20SRC:MED&resulttype=core&format=json

1 October 2019

title

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

1 reference

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1 October 2019

8

N Ascher

1 reference

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1 October 2019

7

J S Najarian

1 reference

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1 October 2019

3

H L Sharp

1 reference

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1 October 2019

2

D K Freese

1 reference

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1 October 2019

author name string

M Tuchman

1

1 reference

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1 October 2019

C B Whitley

4

1 reference

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1 October 2019

M L Ramnaraine

5

1 reference

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1 October 2019

R A Ulstrom

6

1 reference

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1 October 2019

N R Buist

9

1 reference

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1 October 2019

A B Terry

10

1 reference

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1 October 2019

publication date

1 January 1985

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2581063%20AND%20SRC:MED&resulttype=core&format=json

Journal of Inherited Metabolic Disease

1 October 2019

published in

1 reference

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1 October 2019

volume

8

1 reference

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1 October 2019

issue

1

1 reference

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1 October 2019

page(s)

21-24

1 reference

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https://scigraph.springernature.com/pub.10.1007/bf01805479

1 October 2019

exact match

0 references

cites work

The occurrence of hepatoma in the chronic form of hereditary tyrosinemia

1 reference

12 December 2020

Immunosuppressive activity of succinylacetone

1 reference

12 December 2020

On the enzymic defects in hereditary tyrosinemia

1 reference

12 December 2020

Determination of urinary succinylacetone by capillary gas chromatography

1 reference

12 December 2020

Urinary excretion of deuterated metabolites in patients with tyrosinemia type I after oral loading with deuterated L-tyrosine

1 reference

12 December 2020

Deficiency of fumarylacetoacetase in a patient with hereditary tyrosinemia

1 reference

12 December 2020

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

1 reference

12 December 2020

Homotransplantation of the liver in a patientwith hepatoma and hereditary tyrosinemia

1 reference

12 December 2020

On the renal tubular damage in hereditary tyrosinemia and on the formation of succinylacetoacetate and succinylacetone

1 reference

12 December 2020

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

1 reference

12 December 2020

Beta-glucuronidase deficiency mucopolysaccharidosis: methods for enzymatic diagnosis.

1 reference

12 December 2020

Synthetic substrates for alpha-L-iduronidase

1 reference

12 December 2020

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

1 reference

12 December 2020