(Q33591929)

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Peripheral neuropathy as the presenting feature of tyrosinaemia type I and effectively treated with an inhibitor of 4-hydroxyphenylpyruvate dioxygenase

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Europe PubMed Central

PubMed publication ID

28 July 2017

Peripheral neuropathy as the presenting feature of tyrosinaemia type I and effectively treated with an inhibitor of 4-hydroxyphenylpyruvate dioxygenase (English)

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

peripheral neuropathy

1 reference

based on heuristic

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author name string

Gibbs TC

1

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Payan J

2

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Brett EM

3

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Lindstedt S

4

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Holme E

5

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Clayton PT

6

1 reference

Europe PubMed Central

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28 July 2017

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publication date

1 October 1993

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Journal of Neurology, Neurosurgery and Psychiatry

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Europe PubMed Central

PubMed publication ID

28 July 2017

56

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Europe PubMed Central

PubMed publication ID

28 July 2017

10

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

1129-1132

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015246

21 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015246

21 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1015246

21 June 2018

Hematin therapy for the neurologic crisis of tyrosinemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/8410015

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Neonatal screen for hereditary tyrosinaemia type I

1 reference

https://pubmed.ncbi.nlm.nih.gov/8410015

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A modified automated fluorometric method for tyrosine determination in blood spotted on paper: a mass screening procedure for tyrosinemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/8410015

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1136/JNNP.56.10.1129

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

release_mceqh4ahmnbwhgus2d67cxfsre

1 reference

https://api.fatcat.wiki/v0/release/mceqh4ahmnbwhgus2d67cxfsre

24 November 2022

based on heuristic

mapped directly with Wikidata item

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

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