(Q42162886)

17 October 2017

FAMILIAL HEPATIC COPPER STORAGE DISEASE: A VARIANT OF WILSON'S DISEASE. (English)

1 reference

17 October 2017

FISHER MM

1

1 reference

17 October 2017

SHERLOCK S

series ordinal

2

1 reference

17 October 2017

language of work or name

English

0 references

publication date

1 February 1964

1 reference

Archives of Disease in Childhood

17 October 2017

1 reference

17 October 2017

39

1 reference

17 October 2017

14-17

1 reference

Hepatocellular changes in Wilson's disease. Histochemical and electron microscopic studies

17 October 2017

1 reference

PubMed Central

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2019152

ACTIVE 'JUVENILE' CIRRHOSIS CONSIDERED AS PART OF A SYSTEMIC DISEASE AND THE EFFECT OF CORTICOSTEROID THERAPY

26 October 2017

1 reference

PubMed Central

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2019152

Trace metal patterns in disease states. II. Copper storage diseases, with consideration of juvenile cirrhosis, Wilson's disease, and hepatic copper of the newborn

26 October 2017

1 reference

12 December 2020

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

1 reference

12 December 2020

The diagnosis of Wilson's disease in asymptomatic patients

1 reference

12 December 2020

[Wilson's disease of hepatic form in the child and its treatment.]

1 reference

12 December 2020

Caeruioplasmin in liver disease. A diagnostic pitfall

1 reference

12 December 2020

Identifiers

DOI

10.1136/ADC.39.203.14

1 reference

17 October 2017

1 reference

17 October 2017

PubMed publication ID

14160082

1 reference