Discover Community Create You

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

Dopaminergic dysfunction in unrelated, asymptomatic carriers of a single parkin mutation.

Neurology - 13 Dec 2005

Inzelberg Rivka, Hattori Nobutaka, Mizuno Yoshikuni

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Ethnicity
Share to Age of Onset
Share to Dopamine
Share to Genetic Carrier Screening

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Levodopa

Share to Parkinson Disease

Share to Tremor

Share to Ubiquitin-Protein Ligases

Source

Identifiers

PMID: 16344545
DOI: 10.1212/01.wnl.0000200029.57187.05

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Dopaminergic dysfunction in unrelated, asymptomatic carriers of a single parkin mutation.PMID 16344545Read ↗

Dopaminergic dysfunction in unrelated, asymptomatic carriers of a single parkin mutation.Semantic proximity Read ↗

Parkin and Parkinson's disease: differentiated by non-dopaminergic dysfunction?Semantic proximity Read ↗

Expanding phenotype and clinical heterogeneity in patients with identical mutation of the parkin gene.Semantic proximity Read ↗

Gene symbol: PARK2. Disease: Parkinsonism, juvenile, autosomal recessive.Semantic proximity Read ↗

Parkin function in Parkinson's disease.Semantic proximity Read ↗

Heterozygous exon 3 deletion in the Parkin gene in a patient with clinical and radiological MSA-C phenotype.Semantic proximity Read ↗

Deletions in the Parkin gene and genetic heterogeneity in a Greek family with early onset Parkinson's diseaseSemantic proximity Read ↗

Neurocognitive & neuropsychiatric phenotypes of PARK2-associated early-onset Parkinson's disease in two siblings.Semantic proximity Read ↗

Phenotypic variability of parkin mutations in single kindred.Semantic proximity Read ↗

Novel compound heterozygous synaptojanin-1 mutation causes l-dopa-responsive dystonia-parkinsonism syndrome.Semantic proximity Read ↗

Mutations in the parkin gene cause autosomal recessive juvenile parkinsonismSemantic proximity Read ↗

Lewy body pathology and typical Parkinson disease in a patient with a heterozygous (R275W) mutation in the Parkin gene (PARK2).Semantic proximity Read ↗

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