Rapid-onset dystonia-parkinsonism (RDP) is a movement disorder associated with mutations in the ATP1A3 gene. Signs and symptoms of RDP commonly occur in adolescence or early adulthood and can be triggered by physical or psychological stress. Mutations in ATP1A3 are also associated with alternating hemiplegia of childhood (AHC). The neuropathologic substrate of these conditions is unknown. The central nervous system of four siblings, three affected by RDP and one asymptomatic, all carrying the I758S mutation in the ATP1A3 gene, was analyzed. This neuropathologic study is the first carried out in ATP1A3 mutation carriers, whether affected by RDP or AHC. Symptoms began in the third decade of life for two subjects and in the fifth for another. ...
Genetic research has shown that mutations that modify the protein-coding sequence of ATP1A3, the gen...
A 21-year old male presented with ataxia and dysarthria that had appeared over a period of months. E...
Mutations in the ATP1A3 gene, which encodes the alpha3-subunit of sodium-potassium ATPase, are relat...
The allelic disorders rapid-onset dystonia-parkinsonism (RDP), alternating hemiplegia of childhood ...
Rapid‑onset dystonia‑parkinsonism associated with the I758S mutation of the ATP1A3 gene: a neuropath...
Rapid-onset dystonia-parkinsonism (RDP) (also known as DYT12) is characterized by the abrupt onset o...
Neurologic disorders caused by mutations in the ATP1A3 gene were originally reported as three distin...
Rapid-onset dystonia-parkinsonism (RDP) (also known as DYT12) is characterized by the abrupt onset o...
AbstractRapid-onset dystonia-parkinsonism (RDP, DYT12) is a distinctive autosomal-dominant movement ...
Background: ATP1A3-related disorders include rapid-onset dystonia–parkinsonism (RDP or DYT12), alter...
Background and objectives: ATP1A3 is associated with a broad spectrum of predominantly neurological ...
A 21-year old male presented with ataxia and dysarthria that had appeared over a period of months. E...
Genetic research has shown that mutations that modify the protein-coding sequence of ATP1A3, the gen...
Heterozygous mutations in the ATP1A3 gene, coding for an alpha subunit isoform (α3) of Na+/K+-ATPase...
Mutations in the ATP1A3 gene, which encodes the alpha3-subunit of sodium-potassium ATPase, are relat...
Genetic research has shown that mutations that modify the protein-coding sequence of ATP1A3, the gen...
A 21-year old male presented with ataxia and dysarthria that had appeared over a period of months. E...
Mutations in the ATP1A3 gene, which encodes the alpha3-subunit of sodium-potassium ATPase, are relat...
The allelic disorders rapid-onset dystonia-parkinsonism (RDP), alternating hemiplegia of childhood ...
Rapid‑onset dystonia‑parkinsonism associated with the I758S mutation of the ATP1A3 gene: a neuropath...
Rapid-onset dystonia-parkinsonism (RDP) (also known as DYT12) is characterized by the abrupt onset o...
Neurologic disorders caused by mutations in the ATP1A3 gene were originally reported as three distin...
Rapid-onset dystonia-parkinsonism (RDP) (also known as DYT12) is characterized by the abrupt onset o...
AbstractRapid-onset dystonia-parkinsonism (RDP, DYT12) is a distinctive autosomal-dominant movement ...
Background: ATP1A3-related disorders include rapid-onset dystonia–parkinsonism (RDP or DYT12), alter...
Background and objectives: ATP1A3 is associated with a broad spectrum of predominantly neurological ...
A 21-year old male presented with ataxia and dysarthria that had appeared over a period of months. E...
Genetic research has shown that mutations that modify the protein-coding sequence of ATP1A3, the gen...
Heterozygous mutations in the ATP1A3 gene, coding for an alpha subunit isoform (α3) of Na+/K+-ATPase...
Mutations in the ATP1A3 gene, which encodes the alpha3-subunit of sodium-potassium ATPase, are relat...
Genetic research has shown that mutations that modify the protein-coding sequence of ATP1A3, the gen...
A 21-year old male presented with ataxia and dysarthria that had appeared over a period of months. E...
Mutations in the ATP1A3 gene, which encodes the alpha3-subunit of sodium-potassium ATPase, are relat...