Hepatolenticular degeneration (Wilson's disease); a case diagnosed biochemically before clinical manifestations (Q78560797)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13631994%20AND%20SRC:MED&resulttype=core&format=json

15 December 2019

title

Hepatolenticular degeneration (Wilson's disease); a case diagnosed biochemically before clinical manifestations (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13631994%20AND%20SRC:MED&resulttype=core&format=json

15 December 2019

author name string

T LYGREN

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13631994%20AND%20SRC:MED&resulttype=core&format=json

15 December 2019

E W SORENSEN

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13631994%20AND%20SRC:MED&resulttype=core&format=json

15 December 2019

language of work or name

English

0 references

publication date

1 February 1959

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13631994%20AND%20SRC:MED&resulttype=core&format=json

15 December 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13631994%20AND%20SRC:MED&resulttype=core&format=json

15 December 2019

volume

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13631994%20AND%20SRC:MED&resulttype=core&format=json

15 December 2019

issue

7067

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13631994%20AND%20SRC:MED&resulttype=core&format=json

15 December 2019

page(s)

276-277

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13631994%20AND%20SRC:MED&resulttype=core&format=json

Genetic and biochemical aspects of Wilson's disease

15 December 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2859%2990203-X

7 January 2021

Studies on copper metabolism. XI. Copper and iron metabolism in the nephrotic syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2859%2990203-X

7 January 2021

Hepatolenticular degeneration (Wilson's disease) as a form of idiopathic cirrhosis

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2859%2990203-X

7 January 2021

A study of the behaviour of some sixty amino-acids and other ninhydrin-reacting substances on phenol-;collidine' filter-paper chromatograms, with notes as to the occurrence of some of them in biological fluids

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2859%2990203-X

7 January 2021

Studies on copper metabolism. XIV. Copper, ceruloplasmin and oxidase activity in sera of normal human subjects, pregnant women, and patients with infection, hepatolenticular degeneration and the nephrotic syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2859%2990203-X

7 January 2021

Rapid test for hepatolenticular degeneration

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2859%2990203-X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2859%2990203-X

7 January 2021

The amino acid content of the blood and urine in Wilson's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2859%2990203-X

7 January 2021

10.1016/S0140-6736(59)90203-X

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:13631994%20AND%20SRC:MED&resulttype=core&format=json

15 December 2019

1 reference