Background: The most widely recognized aspect of the neuro-hepatic relation is hepatic encephalopathy, in which neurotransmission in the brain is altered. Of course, there are many conditions that affect both the liver and the nervous system, Wilson’s disease being one of the best known. The aim was to characterize the neurological manifestations of Wilson’s diseases in terms of symptom type and degree of neurological impairment and correlate these features with degree of abnormalities in copper metabolism, and hepatic status. Material and methods: 15 patients diagnosed with Wilson’s disease were characterized by examination in terms of symptoms including consciousness, activities of daily living as reported by the patient. The neurolo...
Wilson\u27s disease is a rare autosomal recessive disorder of copper metabolism that often proves a ...
Despite a long history, Wilson's disease, an autosomal recessive disease caused by mutations in the ...
Neuropsychological studies of 34 patients with Wilson's disease differentiated according to specific...
Abstract Background Wilson disease is a rare genetic disorder in which impaired copper excretion res...
Wilson’s disease is an inherited disorder of hepatic copper metabolism, leading to the acc...
Wilson's disease (WD) is an autosomal recessive disorder characterized by copper overload. In this d...
Background: Cognitive impairment is common in neurological presentations of Wilson's disease (WD). ...
ObjectiveWilson disease (WD) is an inherited copper metabolism dysfunction disease characterized by ...
Aim: Wilson's disease (WD) is a hereditary disease that causes the accumulation of copper in many or...
This issue of eMedRef provides information to clinicians on the pathophysiology, diagnosis, and ther...
Wilson’s disease is a rare inborn error of metabolism characterized by abnormal deposition of copper...
Wilson's disease is an autosomal-recessive disorder of copper metabolism with neurological and hepat...
Wilson’s disease is an autosomal-recessive disorder of copper metabolism with neurological and hepat...
Wilson disease (WD) is an inherited disorder of hepatic copper metabolism with considerable variatio...
Wilson disease (WD) is an uncommon recessive genetic disorder affecting copper metabolism. Cardiac,...
Wilson\u27s disease is a rare autosomal recessive disorder of copper metabolism that often proves a ...
Despite a long history, Wilson's disease, an autosomal recessive disease caused by mutations in the ...
Neuropsychological studies of 34 patients with Wilson's disease differentiated according to specific...
Abstract Background Wilson disease is a rare genetic disorder in which impaired copper excretion res...
Wilson’s disease is an inherited disorder of hepatic copper metabolism, leading to the acc...
Wilson's disease (WD) is an autosomal recessive disorder characterized by copper overload. In this d...
Background: Cognitive impairment is common in neurological presentations of Wilson's disease (WD). ...
ObjectiveWilson disease (WD) is an inherited copper metabolism dysfunction disease characterized by ...
Aim: Wilson's disease (WD) is a hereditary disease that causes the accumulation of copper in many or...
This issue of eMedRef provides information to clinicians on the pathophysiology, diagnosis, and ther...
Wilson’s disease is a rare inborn error of metabolism characterized by abnormal deposition of copper...
Wilson's disease is an autosomal-recessive disorder of copper metabolism with neurological and hepat...
Wilson’s disease is an autosomal-recessive disorder of copper metabolism with neurological and hepat...
Wilson disease (WD) is an inherited disorder of hepatic copper metabolism with considerable variatio...
Wilson disease (WD) is an uncommon recessive genetic disorder affecting copper metabolism. Cardiac,...
Wilson\u27s disease is a rare autosomal recessive disorder of copper metabolism that often proves a ...
Despite a long history, Wilson's disease, an autosomal recessive disease caused by mutations in the ...
Neuropsychological studies of 34 patients with Wilson's disease differentiated according to specific...