(Q62024074)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10945671%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

title

Aspartame loading test in PKU heterozygous individuals bearing severe and moderate mutations (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10945671%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

1 reference

1 reference

5

R Giugliani

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10945671%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

author name string

L C da Silva

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10945671%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

T S Carvalho

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10945671%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

F B da Silva

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10945671%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

R F Pires

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10945671%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

M L Pereira

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10945671%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

publication date

1 July 2000

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10945671%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10945671%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

volume

58

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10945671%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

issue

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10945671%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

page(s)

86-88

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10945671%20AND%20SRC:MED&resulttype=core&format=json

PAH Mutation Analysis Consortium Database: 1997. Prototype for relational locus-specific mutation databases

9 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.580118.X

7 January 2021

A European multicenter study of phenylalanine hydroxylase deficiency: classification of 105 mutations and a general system for genotype-based prediction of metabolic phenotype

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.580118.X

7 January 2021

Detection of heterozygous carriers for phenylketonuria by a L-[2H5]phenylalanine stable isotope loading test.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.580118.X

7 January 2021

Heterozygous carriers of classical phenylketonuria in a sample of the turkish population: Detection by a spectrofluorimetric method

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.580118.X

7 January 2021

Aspartame-sweetened beverage: effect on plasma amino acid concentrations in normal adults and adults heterozygous for phenylketonuria

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.580118.X

7 January 2021

Effect of high-protein meal plus aspartame ingestion on plasma phenylalanine concentrations in obligate heterozygotes for phenylketonuria

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.580118.X

7 January 2021

Evaluation of an aspartame loading test for the detection of heterozygotes for classical phenylketonuria.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.580118.X

7 January 2021

Severity of mutation in the phenylalanine hydroxylase gene influences phenylalanine metabolism in phenylketonuria and hyperphenylalaninaemia heterozygotes.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.580118.X

7 January 2021

Phenylalanine and tyrosine metabolism in phenylketonuria heterozygotes: influence of different phenylalanine hydroxylase mutations

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.580118.X

7 January 2021

Aberrant phenylalanine metabolism in phenylketonuria heterozygotes

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2000.580118.X

7 January 2021

10.1034/J.1399-0004.2000.580118.X

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10945671%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

1 reference