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

Cognitive impairment in carriers of glucocerebrosidase gene mutation in Parkinson disease patients.

Neurologia i neurochirurgia polska - 1 Jan 2014

Malec-Litwinowicz Michalina, Rudzińska Monika, Szubiga Michał, Michalski Michał, Tomaszewski Tomasz, Szczudlik Andrzej

Abstract excerpt

AIM: Parkinson disease (PD) is the common neurodegenerative disease with motor and numerous non-motor symptoms, including cognitive impairment. Mutation of glucocerebrosidase (GBA) gene is the most common genetic risk factor of sporadic PD. The aim of this study was to assess clinical features of PD associated with GBA mutation. METHODS: One hundred and thirty-eight PD patients were involved and examined by the...

Read the complete abstract on PubMed

Topics

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

Share to Aged
Share to Cognition Disorders

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Glucosylceramidase

Share to Neuropsychological Tests

Share to Parkinson Disease

Share to Point Mutation

Share to Poland

Share to Risk Factors

Source

Identifiers

PMID: 25168325
DOI: 10.1016/j.pjnns.2014.07.005

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Cognitive impairment in carriers of glucocerebrosidase gene mutation in Parkinson disease patients.PMID 25168325Read ↗

Effects of glucocerebrosidase gene polymorphisms and mutations on the risk of Parkinson's disease dementia: A meta-analysis.Semantic proximity Read ↗

Mutations of glucocerebrosidase gene and susceptibility to Parkinson's disease: An updated meta-analysis in a European population.Semantic proximity Read ↗

Glucocerebrosidase mutations in primary parkinsonism.Semantic proximity Read ↗

GBA Variants Influence Motor and Non-Motor Features of Parkinson's Disease.Semantic proximity Read ↗

Mutations in GBA and risk of Parkinson's disease: a meta-analysis based on 25 case-control studies.Semantic proximity Read ↗

Analysis of the glucocerebrosidase gene in Parkinson's disease.Semantic proximity Read ↗

Association of glucocerebrosidase polymorphisms and mutations with dementia in incident Parkinson's disease.Semantic proximity Read ↗

Mutations in the glucocerebrosidase gene are responsible for Chinese patients with Parkinson's disease.Semantic proximity Read ↗

Glucocerebrosidase mutations in clinical and pathologically proven Parkinson's disease.Semantic proximity Read ↗

Glucocerebrosidase mutations in a Serbian Parkinson's disease population.Semantic proximity Read ↗

Mutations in glucocerebrosidase are a major genetic risk factor for Parkinson's disease and increase susceptibility to dementia in a Flanders-Belgian cohort.Semantic proximity Read ↗

Association Between Glucocerebrosidase Mutations and Parkinson's Disease in IrelandSemantic proximity Read ↗

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