Wilson disease is one of the few movement disorders in which there are therapies that
modify disease progression. This disease is caused by copper overload primarily in the liver …

Wilson's disease is an autosomal–recessive disorder of copper metabolism caused by
mutations in ATP7B and associated with neurological, psychiatric, ophthalmological and …

Wilson's disease (WD) is a rare autosomal recessive disorder of hepatocellular copper
deposition. The diagnostic approach to patients with WD may be challenging and is based …

The global pandemic from COVID-19 infection has generated significant public health
concerns, both health-wise and economically. There is no specific pharmacological antiviral …

Background Conducting a systematic review demands a significant amount of effort in
screening titles and abstracts. To accelerate this process, various tools that utilize active …

Wilson's disease is an autosomal-recessive disorder of copper metabolism with hepatic,
neurological, psychiatric, ophthalmological, haematological, renal, and rheumatological …

Wilson's disease (WD) is a hereditary disorder of copper metabolism, producing abnormally
high levels of non-ceruloplasmin-bound copper, the determinant of the pathogenic process …

Objectives: Review the typical presentation of a patient with zinc toxicity. Describe the
management considerations for patients with zinc toxicity. Outline the treatment options for …

Protein fibrils drive the onset and progression of many diseases in a prion-like manner, ie
they transcellular propagate through the extracellular space to health cells to initiate toxic …

Wilson's disease (WD) is a rare condition caused by copper accumulation primarily in the
liver and secondly in other organs, such as the central nervous system. It is a hereditary …