(Q45341390)

13 December 2017

Decreased serum antioxidant capacity in patients with Wilson disease is associated with neurological symptoms (English)

1 reference

13 December 2017

1 reference

2

1 reference

13 December 2017

5

1 reference

13 December 2017

6

1 reference

13 December 2017

11

1 reference

13 December 2017

Ivana Malikova

10

0 references

Petr Urbánek

object named as

Petr Urbanek

8

0 references

Radan Bruha

object named as

Radan Bruha

1

0 references

author name string

Zdenek Marecek

3

1 reference

13 December 2017

Lenka Pospisilova

4

1 reference

13 December 2017

Jaromir Petrtyl

7

1 reference

13 December 2017

Alena Jiraskova

9

1 reference

13 December 2017

Peter Ferenci

12

1 reference

13 December 2017

3 December 2011

1 reference

Journal of Inherited Metabolic Disease

13 December 2017

1 reference

13 December 2017

35

1 reference

13 December 2017

3

1 reference

13 December 2017

541-548

1 reference

https://scigraph.springernature.com/pub.10.1007/s10545-011-9422-5

13 December 2017

0 references

cites work

Nonalcoholic fatty liver disease

1 reference

https://api.crossref.org/works/10.1007%2FS10545-011-9422-5

Metal-induced hepatotoxicity

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-011-9422-5

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/10.1007%2FS10545-011-9422-5

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-011-9422-5

Diagnosis and phenotypic classification of Wilson disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-011-9422-5

The possible role of copper ions in atherogenesis: the Blue Janus

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-011-9422-5

Potential of vitamin E as an antioxidant adjunct in Wilson's disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-011-9422-5

Chronic exposure of HepG2 cells to excess copper results in depletion of glutathione and induction of metallothionein.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-011-9422-5

Clinical presentation, diagnosis and long-term outcome of Wilson's disease: a cohort study

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-011-9422-5

Children's toxicology from bench to bed--Liver Injury (3): Oxidative stress and anti-oxidant systems in liver of patients with Wilson disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-011-9422-5

Sleep disorders in Wilson's disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-011-9422-5

Genotype-phenotype correlation in Italian children with Wilson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-011-9422-5

Diagnosis and treatment of Wilson disease: an update

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-011-9422-5

Strategies of antioxidant defense

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-011-9422-5

Analysis of the human Atox 1 homologue in Wilson patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-011-9422-5

Is low serum tocopherol in Wilson's disease a significant symptom?

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-011-9422-5

alpha-tocopherol ameliorates oxidant injury in isolated copper-overloaded rat hepatocytes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-011-9422-5

Effect of copper on extracellular levels of key pro-inflammatory molecules in hypothalamic GN11 and primary neurons

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-011-9422-5

The Wilson disease gene is a copper transporting ATPase with homology to the Menkes disease gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-011-9422-5

The Wilson disease gene: spectrum of mutations and their consequences.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-011-9422-5

Oxidative stress-mediated hepatotoxicity of iron and copper: role of Kupffer cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-011-9422-5

Mutation analysis of the ATP7B gene and genotype/phenotype correlation in 227 patients with Wilson disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-011-9422-5

Sonographic detection of basal ganglia lesions in asymptomatic and symptomatic Wilson disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-011-9422-5

Copper-induced translocation of the Wilson disease protein ATP7B independent of Murr1/COMMD1 and Rab7.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-011-9422-5

Hepatocyte GP73 expression in Wilson disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-011-9422-5

Liver mitochondrial membrane crosslinking and destruction in a rat model of Wilson disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-011-9422-5

Fluorescence quenching of dipyridamole associated to peroxyl radical scavenging: a versatile probe to measure the chain breaking antioxidant activity of biomolecules

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS10545-011-9422-5

Measurement of copper in biological samples by flame or electrothermal atomic absorption spectrometry

21 January 2018

1 reference

12 December 2020

The level of serum lipids, vitamin E and low density lipoprotein oxidation in Wilson's disease patients

1 reference

12 December 2020

1 reference

12 December 2020

Genetic analysis of BIRC4/XIAP as a putative modifier gene of Wilson disease

1 reference

12 December 2020

Relationship between oxidative stress and antioxidant systems in the liver of patients with Wilson disease: hepatic manifestation in Wilson disease as a consequence of augmented oxidative stress

1 reference

12 December 2020

Low vitamin E content in plasma of patients with alcoholic liver disease, hemochromatosis and Wilson's disease

1 reference

12 December 2020

Prevention of Wilson's Disease in Asymptomatic Patients

1 reference

12 December 2020

A novel pineal night-specific ATPase encoded by the Wilson disease gene

1 reference

12 December 2020

The H1069Q mutation in ATP7B is associated with late and neurologic presentation in Wilson disease: results of a meta-analysis

1 reference

12 December 2020

Recent developments in derivative ultraviolet/visible absorption spectrophotometery

1 reference

12 December 2020

Long-term follow-up of Wilson Disease: natural history, treatment, mutations analysis and phenotypic correlation

1 reference

12 December 2020

Oxidant injury to hepatic mitochondria in patients with Wilson's disease and Bedlington terriers with copper toxicosis

1 reference

12 December 2020

Detection of the His1069Gln mutation in Wilson disease by rapid polymerase chain reaction

1 reference

12 December 2020

Plasma copper and antioxidant status in Wilson's disease

1 reference

12 December 2020

The impact of apolipoprotein E genotypes on age at onset of symptoms and phenotypic expression in Wilson's disease

1 reference

12 December 2020

Oxidative-phosphorylation defects in liver of patients with Wilson's disease

1 reference

12 December 2020

10.1007/S10545-011-9422-5

Identifiers

DOI

1 reference

Dimensions Publication ID

13 December 2017

0 references

1 reference