Cytochrome oxidase deficiency in Wilson's disease: a suggested ceruloplasmin function (Q36450857)

14 August 2017

Cytochrome oxidase deficiency in Wilson's disease: a suggested ceruloplasmin function (English)

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14 August 2017

Shokeir MH

1

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14 August 2017

Shreffler DC

series ordinal

2

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14 August 2017

language of work or name

English

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publication date

1 March 1969

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Proceedings of the National Academy of Sciences of the United States of America

14 August 2017

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14 August 2017

62

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14 August 2017

3

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14 August 2017

867-872

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INVESTIGATION OF THE AMINOACIDURIA IN WILSON'S DISEASE (HEPATOLENTICULAR DEGENERATION): DEMONSTRATION OF A DEFECT IN RENAL FUNCTION.

14 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=223678

Chromosome preparations of leukocytes cultured from human peripheral blood

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=223678

Exchange of ceruloplasmin copper with ionic Cu64 with reference to 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=223678

Renal function in 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=223678

Studies on copper metabolism. XIII. Hepatolenticular degeneration

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=223678

The amino acid content of the blood and urine in 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=223678

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=223678

Leukocyte oxidase: defective activity in chronic granulomatous 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=223678

Abnormalities of copper metabolism in Wilson's disease and their relationship to the aminoaciduria

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=223678

Oral contraceptives and caeruloplasmin activity.

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=223678

Studies of protein metabolism in hepatolenticular degeneration

28 June 2018

1 reference

12 December 2020

STUDIES ON GLYCOPROTEINS. I. THE CARBOHYDRATE PORTION OF HUMAN CERULOPLASMIN

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12 December 2020

Hepatolenticular degeneration (Wilson's disease)

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12 December 2020

Factors influencing serum ceruloplasmin levels in normal individuals

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12 December 2020

Studies on the state of copper in native and modified human ceruloplasmin

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12 December 2020

Genetic and biochemical aspects of Wilson's disease

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12 December 2020

The mechanism of copper deposition in the liver in hepatolenticular degeneration (Wilson's disease)

1 reference

12 December 2020

Relationships between the copper atoms of caeruloplasmin. I. Studies on the exchange of 64 Cu with caeruloplasmin

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12 December 2020

The Fetish of Experiment

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12 December 2020

Histochemical demonstration of copper in copper-fed rats and in hepatolenticular degeneration

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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

Identifiers

DOI

10.1073/PNAS.62.3.867

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14 August 2017

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14 August 2017

PubMed publication ID

4308098

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