The newborn phenylketonuria screening program in Ontario (Q72489194)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5811698%20AND%20SRC:MED&resulttype=core&format=json

27 October 2019

title

The newborn phenylketonuria screening program in Ontario (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5811698%20AND%20SRC:MED&resulttype=core&format=json

27 October 2019

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=5811698

2 July 2023

publication date

1 August 1969

1 reference

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full work available at URL

27 October 2019

https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/5811698/?tool=EBI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5811698

https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/5811698/pdf/?tool=EBI

2 July 2023

file format

Portable Document Format

online access status

open access

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5811698

https://europepmc.org/articles/PMC1946107

2 July 2023

1 reference

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https://europepmc.org/articles/PMC1946107?pdf=render

2 July 2023

file format

Portable Document Format

online access status

open access

content deliverer

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5811698

Canadian Medical Association Journal

2 July 2023

published in

1 reference

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27 October 2019

volume

101

1 reference

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27 October 2019

issue

4

1 reference

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27 October 2019

page(s)

185-190

1 reference

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Diagnostic and therapeutic implications of persistent hyperphenylalaninemia in an infant heterozygous for the gene of phenylketonuria

27 October 2019

cites work

1 reference

12 December 2020

Transient tyrosinemia of the newborn: dietary and clinical aspects

1 reference

12 December 2020

Case-finding in phenylketonuria: 3. One-way paper chromatography of amino acids in blood

1 reference

12 December 2020

Delayed maturation of tyrosine metabolism in a full-term sibling of a child with phenylketonuria.

1 reference

12 December 2020

PHENYLKETONURIA. A REVIEW OF SOME DEFICITS IN OUR INFORMATION

1 reference

12 December 2020

CASE-FINDING IN PHENYLKETONURIA. I. REPORT OF A SURVEY BY THE COLLEGE OF GENERAL PRACTICE OF CANADA

1 reference

12 December 2020

Identifiers

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5811698%20AND%20SRC:MED&resulttype=core&format=json

27 October 2019

1 reference