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

Biallelic Parkin (PARK2) mutations can cause a bvFTD phenotype without clinically relevant parkinsonism.

Parkinsonism & related disorders - 1 Oct 2018

Zimmermann Milan, Wilke Carlo, Schulte Claudia, Hoffmann Jessica, Klopfer Jasmin, Reimold Matthias, Brockmann Kathrin, Synofzik Matthis

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 Fluorodeoxyglucose F18
Share to Mutation
Share to Parkinsonian Disorders
Share to Phenotype

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Positron-Emission Tomography

Share to Ubiquitin-Protein Ligases

Source

Identifiers

PMID: 29910155
DOI: 10.1016/j.parkreldis.2018.06.006

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Biallelic Parkin (PARK2) mutations can cause a bvFTD phenotype without clinically relevant parkinsonism.PMID 29910155Read ↗

Parkin-associated Parkinson’s diseaseSemantic proximity Read ↗

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

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

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

Parkin and Parkinson disease.Semantic proximity Read ↗

[Parkinson's disease associated with a mutation in the PARK2 gene].Semantic proximity Read ↗

Neuropathology of PARK14 is identical to idiopathic Parkinson's disease.Semantic proximity Read ↗

Mice expressing mutant parkin exhibit hallmark features of Parkinson's disease.Semantic proximity Read ↗

Camptocormia, axial dystonia, and parkinsonism: phenotypic heterogeneity of a parkin mutation.Semantic proximity Read ↗

Parkin gene causing benign autosomal recessive juvenile parkinsonism.Semantic proximity Read ↗

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

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