(Q36061716)

11 August 2017

Effects of amino acid loads on a health infant with the biochemical features of Hartnup disease (English)

1 reference

11 August 2017

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A6073838

30 July 2023

author name string

J. W. Seakins

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A6073838

30 July 2023

R. S. Ersser

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A6073838

30 July 2023

language of work or name

English

0 references

publication date

1 December 1967

1 reference

PMC publication ID

2019892

full work available at URL

11 August 2017

https://europepmc.org/articles/PMC2019892

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A6073838

https://europepmc.org/articles/PMC2019892?pdf=render

30 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%3A6073838

https://syndication.highwire.org/content/doi/10.1136/adc.42.226.682

30 July 2023

1 reference

Crossref

DOI

10.1136/ADC.42.226.682

https://api.crossref.org/works/10.1136/ADC.42.226.682

Archives of Disease in Childhood

30 July 2023

published in

1 reference

11 August 2017

42

1 reference

11 August 2017

226

1 reference

11 August 2017

682-688

1 reference

The intestinal absorption defect in cystinuria

11 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2019892

Hereditary pellagra-like skin rash with temporary cerebellar ataxia, constant renal amino-aciduria, and other bizarre biochemical features

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2019892

An inborn defect in the metabolism of tyrosine in infants on a normal diet

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2019892

Renal clearances of amino acids in normal adults and in patients with aminoaciduria

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2019892

The metabolic disorder in Hartnup disease

11 July 2018

1 reference

12 December 2020

The effect of pyridoxine on tryptophan metabolism in phenylketonuria

1 reference

12 December 2020

HARTNUP DISEASE: A GENETIC MODIFICATION OF INTESTINAL AND RENAL TRANSPORT OF CERTAIN NEUTRAL ALPHA-AMINO ACIDS

1 reference

12 December 2020

BIOCHEMICAL ASPECTS OF THE HARTNUP DISEASE. III. GENERAL DISCUSSION AND CONCLUSIONS

1 reference

12 December 2020

ABSORPTION FROM THE SMALL INTESTINE

1 reference

12 December 2020

Detection of heterozygotes for phenylketonuria

1 reference

12 December 2020

DISORDERS OF AMINO-ACID TRANSPORT

1 reference

12 December 2020

AMINOACIDURIA.

series ordinal

6

1 reference

Crossref

DOI

10.1136/ADC.42.226.682

https://api.crossref.org/works/10.1136/ADC.42.226.682

30 July 2023

Identifiers

DOI

10.1136/ADC.42.226.682

1 reference

11 August 2017

1 reference

PMC publication ID

2019892

11 August 2017

1 reference

PMC publication ID

2019892