Sequential measurements of brain glucose metabolism were carried out in a patient with Wilson's disease, before and after successful treatment with D-penicillamine. They demonstrate an evolution of regional metabolism consistent with clinical improvement. The first study showed marked hypometabolism in the putamen on both sides. The second analysis showed bilateral improvement, with predominant residual deficits in the right putamen, while clinical symptoms of striatal dysfunction persisted on the left side. This observation suggests that positron emission tomography is able to follow the neurological evolution in cases of Wilson's disease
Aims: To report on the diagnostic features, management, and clinical outcome after different treatme...
Background and aims. There are certain areas of uncertainty regarding the best therapeutic approach ...
bWilson disease is a rare, autosomal recessive disorder of copper metabolism, which is char-acterize...
Brain magnetic resonance imaging (MRI) studies on Wilson`s disease (WD) show lack of correlations be...
Patients suffering from Wilson's disease frequently have extrapyramidal symptoms, which are ameliora...
Thirty patients with Wilson's disease (WD) were observed at a movement disorder clinic between 1970 ...
BACKGROUND AND PURPOSE: Wilson disease (WD) is rare but one of the few metabolic disorders that can ...
In more than 50 patients with Wilson's disease (WD) sensorimotor and cognitive deficits were quantif...
BACKGROUND AND PURPOSE: Although brain MR imaging findings in adult Wilson disease have been describ...
BACKGROUND AND PURPOSE: Although previous brain imaging studies of Wilson disease (WD) focused on th...
BACKGROUND AND STUDY AIMS: Detailed data on long-term effectiveness of various drug therapies in Wil...
BACKGROUND AND PURPOSE: Although brain MR imaging findings in adult Wilson disease have been describ...
Purpose To evaluate the impact of brain MRI and single-photon emission computed tomography (SPECT) i...
Wilson's disease is an autosomal-recessive disorder of copper metabolism with neurological and hepat...
A 9-year-old boy with asymptomatic Wilson disease who developed neurologic symptoms after treatment ...
Aims: To report on the diagnostic features, management, and clinical outcome after different treatme...
Background and aims. There are certain areas of uncertainty regarding the best therapeutic approach ...
bWilson disease is a rare, autosomal recessive disorder of copper metabolism, which is char-acterize...
Brain magnetic resonance imaging (MRI) studies on Wilson`s disease (WD) show lack of correlations be...
Patients suffering from Wilson's disease frequently have extrapyramidal symptoms, which are ameliora...
Thirty patients with Wilson's disease (WD) were observed at a movement disorder clinic between 1970 ...
BACKGROUND AND PURPOSE: Wilson disease (WD) is rare but one of the few metabolic disorders that can ...
In more than 50 patients with Wilson's disease (WD) sensorimotor and cognitive deficits were quantif...
BACKGROUND AND PURPOSE: Although brain MR imaging findings in adult Wilson disease have been describ...
BACKGROUND AND PURPOSE: Although previous brain imaging studies of Wilson disease (WD) focused on th...
BACKGROUND AND STUDY AIMS: Detailed data on long-term effectiveness of various drug therapies in Wil...
BACKGROUND AND PURPOSE: Although brain MR imaging findings in adult Wilson disease have been describ...
Purpose To evaluate the impact of brain MRI and single-photon emission computed tomography (SPECT) i...
Wilson's disease is an autosomal-recessive disorder of copper metabolism with neurological and hepat...
A 9-year-old boy with asymptomatic Wilson disease who developed neurologic symptoms after treatment ...
Aims: To report on the diagnostic features, management, and clinical outcome after different treatme...
Background and aims. There are certain areas of uncertainty regarding the best therapeutic approach ...
bWilson disease is a rare, autosomal recessive disorder of copper metabolism, which is char-acterize...