(Q34986772)

5 August 2017

title

Homocystinuria in New South Wales (English)

1 reference

5 August 2017

1 reference

B. Wilcken

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A646432

18 July 2022

G. Turner

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A646432

18 July 2022

language of work or name

English

0 references

publication date

1 March 1978

1 reference

full work available at URL

5 August 2017

https://europepmc.org/articles/PMC1545146

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A646432

https://europepmc.org/articles/PMC1545146?pdf=render

18 July 2022

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%3A646432

https://syndication.highwire.org/content/doi/10.1136/adc.53.3.242

18 July 2022

1 reference

https://api.crossref.org/works/10.1136/ADC.53.3.242

Archives of Disease in Childhood

3 September 2023

published in

1 reference

5 August 2017

volume

53

1 reference

5 August 2017

issue

3

1 reference

5 August 2017

page(s)

242-245

1 reference

HOMOCYSTINURIA: AN ENZYMATIC DEFECT.

5 August 2017

cites work

1 reference

PubMed Central

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1545146

Metabolic Abnormalities Detected in a Survey of Mentally Backward Individuals in Northern Ireland

8 July 2018

1 reference

PubMed Central

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1545146

Homocystinuria: Reduced folate levels during pyridoxine treatment

8 July 2018

1 reference

PubMed Central

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1545146

HOMOCYSTINURIA DUE TO CYSTATHIONINE SYNTHETASE DEFICIENCY: THE MODE OF INHERITANCE

8 July 2018

1 reference

12 December 2020

Combined vitamin responsiveness in homocystinuria

1 reference

12 December 2020

Studies of the mechanism of pyridoxine-responsive homocystinuria

1 reference

12 December 2020

Frequency of inborn errors of metabolism, especially PKU, in some representative newborn screening centers around the world: a collaborative study

1 reference

12 December 2020

Detection of abnormal sulphur-containing amino acid excretion in a mass urine-screening programme

1 reference

12 December 2020

Identifiers

DOI

10.1136/ADC.53.3.242

1 reference

5 August 2017

1 reference

5 August 2017

1 reference