DETECTION OF THE HETEROZYGOUS CARRIER OF THE WILSON'S DISEASE GENE. (Q34010551)

30 July 2017

DETECTION OF THE HETEROZYGOUS CARRIER OF THE WILSON'S DISEASE GENE. (English)

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30 July 2017

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Sternlier I

1

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30 July 2017

Morell AG

2

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30 July 2017

Bauer CD

3

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30 July 2017

Combes B

4

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30 July 2017

De Bobes-Sternberg S

5

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30 July 2017

Schein-Berg IH

6

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30 July 2017

language of work or name

English

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publication date

1 April 1961

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Journal of Clinical Investigation

30 July 2017

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30 July 2017

40

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30 July 2017

4

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30 July 2017

707-715

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Sickle cell anemia, a molecular disease

30 July 2017

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=290777

Observations on ceruloplasmin in Wilson's disease

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=290777

Metabolic studies in Wilson's disease using Cu64

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=290777

Genetic basis of the thalassaemia diseases

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=290777

Copper metabolism in normal adults and in clinically normal relatives of patients with Wilson's disease

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=290777

Exchange of ceruloplasmin copper with ionic Cu64 with reference to Wilson's disease

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=290777

Studies on copper metabolism. XIV. Radioactive copper studies in normal subjects and in patients with hepatolenticular degeneration

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=290777

Studies on copper metabolism. XIII. Hepatolenticular degeneration

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=290777

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

5 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=290777

Genetic and biochemical aspects of Wilson's disease

5 July 2018

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12 December 2020

[Considerations on Wilson's disease; genealogic, clinical, and metabolic investigations on 60 members of one family]

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12 December 2020

Metabolism of copper in Wilson's disease and in normal subjects; studies with Cu-64

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12 December 2020

Rapid test for hepatolenticular degeneration

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12 December 2020

Copper transport and excretion in normal subjects and in patients with Laennec's cirrhosis and Wilson's disease: a study with CU64

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12 December 2020

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

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12 December 2020

[Starch gel electrophoresis of human blood & ceruloplasmin identification in normal subjects as well as in homozygote & heterozygote subjects for Wilson's disease gene.]

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12 December 2020

Current views on the pathogenesis and treatment of Wilson's disease

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12 December 2020

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12 December 2020

The long term management of hepatolenticular degeneration (Wilson's disease)

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12 December 2020

A rapid screening test for deficiency of plasma ceruloplasmin and its value in the diagnosis of Wilson's disease

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12 December 2020

A genetical analysis of thirty families with Wilson's disease (hepatolenticular degeneration)

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12 December 2020

Studies on copper metabolism. XXIX. A critical analysis of serum copper and ceruloplasmin concentrations in normal subjects, patients with Wilson's disease and relatives of patients with Wilson's disease

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12 December 2020

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12 December 2020

Heterogeneity of Human Ceruloplasmin

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12 December 2020

The Liver in Wilson’s Disease

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12 December 2020

The Pathogenesis and Clinical Significance of the Liver Disease in Hepatolenticular Degeneration (Wilson's Disease)

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12 December 2020

Identifiers

DOI

10.1172/JCI104304

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30 July 2017

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30 July 2017

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