(Q46910574)

26 December 2017

title

Renal function in tyrosinaemia type I after liver transplantation: a long-term follow-up (English)

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26 December 2017

main subject

liver transplantation

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L J W M Pierik

1

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26 December 2017

F J van Spronsen

series ordinal

2

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26 December 2017

C M A Bijleveld

series ordinal

3

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26 December 2017

C M L van Dael

series ordinal

4

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26 December 2017

publication date

1 January 2005

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26 December 2017

Journal of Inherited Metabolic Disease

published in

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26 December 2017

volume

28

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26 December 2017

issue

6

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26 December 2017

page(s)

871-876

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26 December 2017

https://scigraph.springernature.com/pub.10.1007/s10545-005-0059-0

exact match

0 references

cites work

Assay, properties and tissue distribution of p-hydroxyphenylpyruvate hydroxylase.

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS10545-005-0059-0

Physiological basis for an animal model of the renal Fanconi syndrome: use of succinylacetone in the rat

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS10545-005-0059-0

Tyrosinemia: the Quebec experience

21 January 2018

1 reference

12 December 2020

The occurrence of hepatoma in the chronic form of hereditary tyrosinemia

1 reference

12 December 2020

Tyrosinaemia--treatment and outcome

1 reference

12 December 2020

Tyrosinaemia type I: considerations of treatment strategy and experiences with risk assessment, diet and transplantation

1 reference

12 December 2020

The effects of early treatment of hereditary tyrosinemia type I in infancy by orthotopic liver transplantation.

1 reference

12 December 2020

Liver transplantation for hereditary tyrosinemia--early transplantation following the patient's stabilization

1 reference

12 December 2020

Rapid improvement in the renal tubular dysfunction associated with tyrosinemia following hepatic replacement

1 reference

12 December 2020

Renal failure in adult patients with hereditary tyrosinaemia type I

1 reference

12 December 2020

Homotransplantation of the liver in a patientwith hepatoma and hereditary tyrosinemia

1 reference

12 December 2020

From toxicological problem to therapeutic use: the discovery of the mode of action of 2-(2-nitro-4-trifluoromethylbenzoyl)-1,3-cyclohexanedione (NTBC), its toxicology and development as a drug

1 reference

12 December 2020

Treatment of hereditary tyrosinaemia type I by inhibition of 4-hydroxyphenylpyruvate dioxygenase

1 reference

12 December 2020

Hereditary tyrosinemia type I: a new clinical classification with difference in prognosis on dietary treatment.

1 reference

12 December 2020

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

1 reference

12 December 2020

Indications and outcome of liver transplantation in tyrosinaemia type 1

1 reference

12 December 2020

Resolution of the clinical features of tyrosinemia following orthotopic liver transplantation for hepatoma

1 reference

12 December 2020

Determination of succinylacetone and succinylacetoacetate in physiological samples as the common product 5(3)-methyl-3(5)-isoxazole propionic acid using an isotope dilution method and mass spectrometry

1 reference

12 December 2020

The Nephropathy of Type I Tyrosinemia after Liver Transplantation

1 reference

12 December 2020

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

1 reference

12 December 2020

Liver transplantation in a 23-year-old tyrosinaemia patient: effects on the renal tubular dysfunction

1 reference

12 December 2020

Tyrosinaemia type I: orthotopic liver transplantation as the only definitive answer to a metabolic as well as an oncological problem

1 reference

12 December 2020

Tyrosinaemia type I and NTBC (2-(2-nitro-4-trifluoromethylbenzoyl)-1,3-cyclohexanedione).

1 reference

12 December 2020

10.1007/S10545-005-0059-0

Identifiers

DOI

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26 December 2017

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26 December 2017