(Q43549558)

24 November 2017

title

Iron metabolism and the role of HFE gene polymorphisms in Wilson disease (English)

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24 November 2017

Jan Pfeiffenberger

1

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24 November 2017

Daniel N Gotthardt

2

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24 November 2017

Thomas Herrmann

3

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24 November 2017

Jessica Seessle

4

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24 November 2017

Uta Merle

5

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24 November 2017

Peter Schirmacher

6

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24 November 2017

Wolfgang Stremmel

7

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24 November 2017

Karl Heinz Weiss

8

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24 November 2017

publication date

17 October 2011

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24 November 2017

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24 November 2017

volume

32

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24 November 2017

issue

1

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24 November 2017

page(s)

165-170

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Wilson disease: clinical presentation, treatment, and survival

24 November 2017

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1478-3231.2011.02661.X

The Wilson disease gene: spectrum of mutations and their consequences

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1478-3231.2011.02661.X

The Wilson disease gene is a putative copper transporting P-type ATPase similar to the Menkes gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1478-3231.2011.02661.X

The copper-iron chronicles: the story of an intimate relationship

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1478-3231.2011.02661.X

Identification of the thiol groups in human ceruloplasmin.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1478-3231.2011.02661.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1478-3231.2011.02661.X

Value of an enzymatic assay for the determination of serum ceruloplasmin

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1478-3231.2011.02661.X

Serum ceruloplasmin oxidase activity is a sensitive and highly specific diagnostic marker for Wilson's disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1478-3231.2011.02661.X

Evidence for a critical role of ceruloplasmin oxidase activity in iron metabolism of Wilson disease gene knockout mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1478-3231.2011.02661.X

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1478-3231.2011.02661.X

Abnormal hepatic iron accumulation in LEC rats.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1478-3231.2011.02661.X

Iron accumulation in the liver of male patients with Wilson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1478-3231.2011.02661.X

Compound overload of copper and iron in patients with Wilson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1478-3231.2011.02661.X

Effect of penicillamine and zinc on iron metabolism in Wilson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1478-3231.2011.02661.X

A population-based study of the clinical expression of the hemochromatosis gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1478-3231.2011.02661.X

Effect of treatment of Wilson's disease on natural history of haemochromatosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1478-3231.2011.02661.X

Diagnosis and phenotypic classification of Wilson disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1478-3231.2011.02661.X

Hemochromatosis and transferrin receptor gene polymorphisms in chronic hepatitis C: impact on iron status, liver injury and HCV genotype.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1478-3231.2011.02661.X

The transition metals copper and iron in neurodegenerative diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1478-3231.2011.02661.X

Reactive oxygen species regulate ceruloplasmin by a novel mRNA decay mechanism involving its 3'-untranslated region: implications in neurodegenerative diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1478-3231.2011.02661.X

Global prevalence of putative haemochromatosis mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1478-3231.2011.02661.X

Role of ceruloplasmin in cellular iron uptake

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1478-3231.2011.02661.X

Aceruloplasminemia, an inherited disorder of iron metabolism

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1478-3231.2011.02661.X

Wilson's disease: long-term follow-up of a cohort of 24 patients treated with D-penicillamine.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1478-3231.2011.02661.X

Hereditary hemochromatosis: insights from the Hemochromatosis and Iron Overload Screening (HEIRS) Study

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1478-3231.2011.02661.X

10.1111/J.1478-3231.2011.02661.X

21 January 2018

Identifiers

DOI

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24 November 2017

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