Background: Wilson's disease (WD) is a copper metabolism disorder that causes hepatolenticular degeneration. It is important to diagnose WD before central nervous system involvement
Wilson's disease in an autosomal recessive disorder of copper metabolism where systemic manifestatio...
The diagnosis of Wilson disease (WD) is challenging, especially in children. Early detection is desi...
Wilson disease (WD) is an inherited disorder of hepatic copper metabolism with considerable variatio...
Background: Wilson's disease (WD) is a copper metabolism disorder that causes hepatolenticular degen...
Objectives: Wilson's disease (WD) is characterized with the accumulation of copper in the liver and ...
Wilson disease (WD) is an uncommon autosomal recessive condition of impared hepatic copper excretion...
Clinical presentations of Wilson's disease (WD) in childhood ranges from asymptomatic liver disease ...
ObjectiveWilson disease (WD) is an inherited copper metabolism dysfunction disease characterized by ...
Wilson's disease is an autosomal-recessive disorder of copper metabolism with neurological and hepat...
It is well known that patients with Wilson’s disease (WD) suffer copper metabolism disorder. However...
Abstract Background Wilson disease is a rare genetic disorder in which impaired copper excretion res...
BACKGROUND: Clinical presentations of Wilson's disease (WD) in childhood ranges from asymptomatic li...
Aim: Wilson's disease (WD) is a hereditary disease that causes the accumulation of copper in many or...
Wilson's disease in an autosomal recessive disorder of copper metabolism where systemic manifestatio...
The diagnosis of Wilson disease (WD) is challenging, especially in children. Early detection is desi...
Wilson disease (WD) is an inherited disorder of hepatic copper metabolism with considerable variatio...
Background: Wilson's disease (WD) is a copper metabolism disorder that causes hepatolenticular degen...
Objectives: Wilson's disease (WD) is characterized with the accumulation of copper in the liver and ...
Wilson disease (WD) is an uncommon autosomal recessive condition of impared hepatic copper excretion...
Clinical presentations of Wilson's disease (WD) in childhood ranges from asymptomatic liver disease ...
ObjectiveWilson disease (WD) is an inherited copper metabolism dysfunction disease characterized by ...
Wilson's disease is an autosomal-recessive disorder of copper metabolism with neurological and hepat...
It is well known that patients with Wilson’s disease (WD) suffer copper metabolism disorder. However...
Abstract Background Wilson disease is a rare genetic disorder in which impaired copper excretion res...
BACKGROUND: Clinical presentations of Wilson's disease (WD) in childhood ranges from asymptomatic li...
Aim: Wilson's disease (WD) is a hereditary disease that causes the accumulation of copper in many or...
Wilson's disease in an autosomal recessive disorder of copper metabolism where systemic manifestatio...
The diagnosis of Wilson disease (WD) is challenging, especially in children. Early detection is desi...
Wilson disease (WD) is an inherited disorder of hepatic copper metabolism with considerable variatio...
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