(Q36615959)

15 August 2017

Reduced oxidase activity in the caeruloplasmin of two families with Wilson's disease (English)

1 reference

15 August 2017

J. L. Gollan

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A838874

1 August 2022

J. Stocks

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A838874

1 August 2022

T. L. Dormandy

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A838874

1 August 2022

S. Sherlock

series ordinal

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A838874

1 August 2022

language of work or name

English

0 references

publication date

1 January 1977

1 reference

PMC publication ID

476651

full work available at URL

15 August 2017

https://europepmc.org/articles/PMC476651

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A838874

https://europepmc.org/articles/PMC476651?pdf=render

1 August 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%3A838874

Journal of Clinical Pathology

1 August 2022

published in

1 reference

15 August 2017

30

1 reference

15 August 2017

1

1 reference

15 August 2017

81-83

1 reference

DETECTION OF THE HETEROZYGOUS CARRIER OF THE WILSON'S DISEASE GENE.

15 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=476651

Deficiency of ceruloplasmin in patients with hepatolenticular degeneration (Wilson's disease).

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=476651

A genetic study of Wilson's disease: evidence for heterogeneity

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=476651

The purification of human caeruloplasmin

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=476651

A clinical and biochemical study of hepatolenticular degeneration (Wilson's disease)

28 June 2018

1 reference

12 December 2020

Genetic and biochemical aspects of Wilson's disease

1 reference

12 December 2020

Prevention of Wilson's Disease in Asymptomatic Patients

1 reference

12 December 2020

Heterogeneity of Human Ceruloplasmin

1 reference

12 December 2020

Wilson's disease and the concentration of caeruloplasmin in serum

1 reference

12 December 2020

Identifiers

DOI

10.1136/JCP.30.1.81

1 reference

15 August 2017

1 reference

PMC publication ID

476651

15 August 2017

1 reference

PMC publication ID

476651