Context.—: Recently, an exchangeable copper (CuEXC) assay has been suggested as a robust and feasible diagnostic tool for Wilson disease (WD). Although WD is a disorder that requires lifelong treatment and monitoring, few data are currently available regarding the status of copper levels in children. Objective.—: To evaluate the performance of copper assays and establish a reference interval for total copper and CuEXC in the pediatric population. Design.—: Serum samples from children aged 1-5 (n = 122), 6-12 (n = 125), and 13-18 years (n = 120) were analyzed. Total copper and CuEXC concentrations were directly measured using inductively coupled plasma mass spectrometry, and relative CuEXC levels were calculated. Total copper reference int...
Objective: Wilson's disease (WD) is an autosomal recessive disease with genetic abnormality on ...
The diagnosis of Wilson disease (WD) is challenging, especially in children. Early detection is desi...
International audienceWilson disease (WD) is an autosomal recessive disorder of copper (Cu) metaboli...
Introduction. Wilson”s disease (WD) biochemical markers continue to evolve. Classical tests have th...
Wilson's disease (WD) is a genetic disorder affecting Cu metabolism, which can lead to severe physio...
International audienceWilson's disease (WD) is caused by mutations in the ATP7B gene responsible for...
An improved method for the study of copper metabolism in Wilson's disease, using a stable, rather th...
Background: Urinary copper excretion higher than 100 mu g/24 h is useful for diagnosing Wilson's dis...
International audienceBackground & Aims: Measuring of the relative exchangeable copper seems to be a...
Objectives and Study: Wilson disease (WD) is an autosomal recessive disorder of copper metabolism r...
The diagnosis of Wilson disease (WD) is challenging, especially in children. Early detection is desi...
Information about Cu fractionation and Cu isotopic composition can be paramount when investigating W...
Artículo de publicación ISIIt is not clear how frequent is copper deficiency in humans. Current copp...
Objective: Wilson's disease (WD) is an autosomal recessive disease with genetic abnormality on ...
The diagnosis of Wilson disease (WD) is challenging, especially in children. Early detection is desi...
International audienceWilson disease (WD) is an autosomal recessive disorder of copper (Cu) metaboli...
Introduction. Wilson”s disease (WD) biochemical markers continue to evolve. Classical tests have th...
Wilson's disease (WD) is a genetic disorder affecting Cu metabolism, which can lead to severe physio...
International audienceWilson's disease (WD) is caused by mutations in the ATP7B gene responsible for...
An improved method for the study of copper metabolism in Wilson's disease, using a stable, rather th...
Background: Urinary copper excretion higher than 100 mu g/24 h is useful for diagnosing Wilson's dis...
International audienceBackground & Aims: Measuring of the relative exchangeable copper seems to be a...
Objectives and Study: Wilson disease (WD) is an autosomal recessive disorder of copper metabolism r...
The diagnosis of Wilson disease (WD) is challenging, especially in children. Early detection is desi...
Information about Cu fractionation and Cu isotopic composition can be paramount when investigating W...
Artículo de publicación ISIIt is not clear how frequent is copper deficiency in humans. Current copp...
Objective: Wilson's disease (WD) is an autosomal recessive disease with genetic abnormality on ...
The diagnosis of Wilson disease (WD) is challenging, especially in children. Early detection is desi...
International audienceWilson disease (WD) is an autosomal recessive disorder of copper (Cu) metaboli...