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

Neurologic symptoms in Wilson disease (WD) appear at an older age compared to hepatic
symptoms and manifest in patients with misdiagnosed liver disease, in patients when the …

This fully updated edition of Developmental Neuropsychology: A Clinical Approach
addresses key issues in child neuropsychology with a unique emphasis on evidence …

The copper (Cu) transporters ATPase copper-transporting alpha (ATP7A) and ATPase
copper-transporting beta (ATP7B) are essential for the normal function of the mammalian …

Background Wilson's disease (WD) is a rare autosomal recessive disorder of copper
metabolism. If untreated, WD, which is initially a liver disease, can turn into a multi-systemic …

Background Cognitive impairment is common in neurological presentations of Wilson's
disease (WD). Various domains can be affected, and subclinical deficits have been reported …

Objective: Cognitive deficits in patients with Wilson's disease (WD) have been reported in
several studies, but there was no detailed analysis of the various components of attention …

Wilson disease–can present with such a variety of psychiatric and cognitive symptoms that it
has been named the “great masquerader.” Symptoms may include cognitive deficits …

Objectives To evaluate the cognitive performance of a group of patients with W ilson's
disease (WD) and to correlate the cognitive findings with changes in magnetic resonance …

Objectives: Pediatric acute liver failure (PALF) is a rare but serious event, with poorly
understood functional outcomes. The goal was to determine the prevalence of reduced …