(Q39971419)

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Phenylalaninemia

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scholarly article

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Europe PubMed Central

16 September 2017

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Europe PubMed Central

Phenylalaninemia (English)

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10.1016/S0031-3955(16)32124-1

https://api.crossref.org/works/10.1016/S0031-3955(16)32124-1

13 March 2023

author name string

G. G. Carpenter

1

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A4871768

13 March 2023

V. H. Auerbach

2

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A4871768

13 March 2023

A. M. DiGeorge

3

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A4871768

13 March 2023

language of work or name

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=4871768

13 March 2023

publication date

1 May 1968

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Europe PubMed Central

16 September 2017

full work available at URL

https://api.elsevier.com/content/article/PII:S0031395516321241?httpAccept=text/xml

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10.1016/S0031-3955(16)32124-1

https://api.crossref.org/works/10.1016/S0031-3955(16)32124-1

13 March 2023

https://api.elsevier.com/content/article/PII:S0031395516321241?httpAccept=text/plain

1 reference

10.1016/S0031-3955(16)32124-1

https://api.crossref.org/works/10.1016/S0031-3955(16)32124-1

13 March 2023

Pediatric Clinics of North America

1 reference

Europe PubMed Central

16 September 2017

15

1 reference

Europe PubMed Central

16 September 2017

313-323

1 reference

Europe PubMed Central

16 September 2017

2

1 reference

Europe PubMed Central

16 September 2017

Identification of heterozygotes with phenylketonuria on basis of blood tyrosine responses

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2816%2932124-1

7 January 2021

based on heuristic

inferred from DOI database lookup

GENETIC MECHANISMS PRODUCING MULTIPLE ENZYME DEFECTS. A REVIEW OF UNEXPLAINED CASES AND A NEW HYPOTHESIS

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2816%2932124-1

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2816%2932124-1

7 January 2021

based on heuristic

inferred from DOI database lookup

Conference on treatment of phenylketonuria

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2816%2932124-1

7 January 2021

based on heuristic

inferred from DOI database lookup

THE PRIMARY AMINO-ACIDOPATHIES. GENETIC DEFECTS IN THE METABOLISM OF THE AMINO ACIDS.

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2816%2932124-1

7 January 2021

based on heuristic

inferred from DOI database lookup

Cystathioninuria: nature of the defect

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2816%2932124-1

7 January 2021

based on heuristic

inferred from DOI database lookup

Serum phenylalanine and tyrosine levels in the newborn infant

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2816%2932124-1

7 January 2021

based on heuristic

inferred from DOI database lookup

Phenylalanine-hydroxylase activity in hyperphenylalaninaemia

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2816%2932124-1

7 January 2021

based on heuristic

inferred from DOI database lookup

Aminoacidemia of prematurity. Its response to ascorbic acid

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2816%2932124-1

7 January 2021

based on heuristic

inferred from DOI database lookup

Diagnosis of phenylketonuria (phenylalanine hydroxylase deficiency, temporary and permanent).

1 reference

https://api.crossref.org/works/10.1016%2FS0031-3955%2816%2932124-1

7 January 2021

based on heuristic

inferred from DOI database lookup

THE METABOLISM OF PHENYLALANINE AND TYROSINE IN THE PREMATURE INFANT

19

1 reference

10.1016/S0031-3955(16)32124-1

https://api.crossref.org/works/10.1016/S0031-3955(16)32124-1

13 March 2023

Hyperphenylalaninemia without phenylketonuria

20

1 reference

10.1016/S0031-3955(16)32124-1

https://api.crossref.org/works/10.1016/S0031-3955(16)32124-1

13 March 2023

Identifiers

10.1016/S0031-3955(16)32124-1

0 references

1 reference

Europe PubMed Central

16 September 2017

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