Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Rapid-onset dystonia-parkinsonism in a child with a novel atp1a3 gene mutation.

Neurology - 4 Aug 2009

Anselm I A, Sweadner K J, Gollamudi S, Ozelius L J, Darras B T

Abstract excerpt

No abstract is available from the source.

Topics

Join the communities discussing this publication.

Acute Disease
Age of Onset
Deglutition Disorders
Dystonic Disorders
Muscle Hypotonia
Parkinsonian Disorders
Positron-Emission Tomography

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Sodium-Potassium-Exchanging ATPase

Source

Open in PubMed Open full text

Identifiers

PMID: 19652145
DOI: 10.1212/WNL.0b013e3181b04acd
PMCID: PMC2833268

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026.

Community interpretation

Discuss the evidence

Ask a question, add context or challenge an interpretation. Community activity is separate from scientific evidence strength.

0

discussions

0

replies

Citations encouraged

Claims remain attributable.

No discussion yet

Be the first to add a careful, cited interpretation.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Rapid-onset dystonia-parkinsonism in a child with a novel atp1a3 gene mutation.PMID 19652145Read ↗

A novel de-novo mutation in the ATP1A3 gene causing rapid-onset dystonia parkinsonism.Semantic proximity Read ↗

Different phenotypes of neurological diseases, including alternating hemiplegia of childhood and rapid-onset dystonia-parkinsonism, caused by de novo ATP1A3 mutation in a family.Semantic proximity Read ↗

A novel ATP1A3 mutation with unique clinical presentation.Semantic proximity Read ↗

ATP1A3 mutation in rapid-onset dystonia parkinsonism: New data and genotype-phenotype correlation analysisSemantic proximity Read ↗

Atypical presentation of rapid-onset dystonia-parkinsonism in a toddler with a novel mutation in the ATP1A3 gene.Semantic proximity Read ↗

ATP1A3 mutations in infants: a new rapid-onset dystonia-Parkinsonism phenotype characterized by motor delay and ataxia.Semantic proximity Read ↗

The expanding clinical and genetic spectrum of ATP1A3-related disorders.Semantic proximity Read ↗

The diagnostic spectrum of ATP1A3-related disorders: 3 new patients.Semantic proximity Read ↗

[A childhood-onset rapid-onset dystonia parkinsonism family with ATP1A3 gene mutation and literatures review].Semantic proximity Read ↗

A novel presentation of an ATP1A3 gene mutation - case report and literature review.Semantic proximity Read ↗

ATP1A3-related disorders: An update.Semantic proximity Read ↗

Childhood Rapid-Onset Ataxia: Expanding the Phenotypic Spectrum of ATP1A3 Mutations.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.