Introduction. Wilson”s disease (WD) biochemical markers continue to evolve. Classical tests have their own limits (tab.1), and they are often insufficient to diagnose or exclude WD. The free copper was proposed as a diagnostic test, but it was showed a large overlapping of this parameter between non-WD subjects and WD patients. New biomarkers are being investigated. Purpose. The paper aims to analyze the bibliographic data on the new tools for diagnostic in WD, like exchangeable copper (CuEXC). Material and methods. An advanced search was performed in the PubMed, and ScienceDirect databases, using the search English terms: ”Wilson's disease”, ”diagnostic test” and ”relative exchangeable copper”. Results. CuEXC is a new va...
An improved method for the study of copper metabolism in Wilson's disease, using a stable, rather th...
Aims: The histochemical demonstration of hepatic copper is important in the diagnosis of Wilson's di...
International audienceWilson disease (WD) is an autosomal recessive disorder of copper (Cu) metaboli...
International audienceBackground & Aims: Measuring of the relative exchangeable copper seems to be a...
International audienceWilson's disease (WD) is caused by mutations in the ATP7B gene responsible for...
Context.—: Recently, an exchangeable copper (CuEXC) assay has been suggested as a robust and feasibl...
Introduction. Wilson’s disease - a genetic disorder due to mutations of the ATP7B gene which causes ...
Information about Cu fractionation and Cu isotopic composition can be paramount when investigating W...
Wilson's disease is an autosomal recessive disorder of copper metabolism. The culprit gene is ATP7B....
Wilson's disease (WD) is an inherited disorder of copper metabolism leading to liver failure and/or ...
The diagnosis of Wilson disease (WD) is challenging, especially in children. Early detection is desi...
Wilson's disease (WD) is a genetic disorder affecting Cu metabolism, which can lead to severe physio...
BACKGROUND: Wilson\u27s disease (WD) is an inherited disorder of copper metabolism leading to liver...
An improved method for the study of copper metabolism in Wilson's disease, using a stable, rather th...
Aims: The histochemical demonstration of hepatic copper is important in the diagnosis of Wilson's di...
International audienceWilson disease (WD) is an autosomal recessive disorder of copper (Cu) metaboli...
International audienceBackground & Aims: Measuring of the relative exchangeable copper seems to be a...
International audienceWilson's disease (WD) is caused by mutations in the ATP7B gene responsible for...
Context.—: Recently, an exchangeable copper (CuEXC) assay has been suggested as a robust and feasibl...
Introduction. Wilson’s disease - a genetic disorder due to mutations of the ATP7B gene which causes ...
Information about Cu fractionation and Cu isotopic composition can be paramount when investigating W...
Wilson's disease is an autosomal recessive disorder of copper metabolism. The culprit gene is ATP7B....
Wilson's disease (WD) is an inherited disorder of copper metabolism leading to liver failure and/or ...
The diagnosis of Wilson disease (WD) is challenging, especially in children. Early detection is desi...
Wilson's disease (WD) is a genetic disorder affecting Cu metabolism, which can lead to severe physio...
BACKGROUND: Wilson\u27s disease (WD) is an inherited disorder of copper metabolism leading to liver...
An improved method for the study of copper metabolism in Wilson's disease, using a stable, rather th...
Aims: The histochemical demonstration of hepatic copper is important in the diagnosis of Wilson's di...
International audienceWilson disease (WD) is an autosomal recessive disorder of copper (Cu) metaboli...