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

Presenilin-2 gene mutation presenting as Lewy body dementia?

Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology - 1 Jun 2011

Raciti Loredana, Nicoletti Alessandra, Le Pira Francesco, Andreoli Virginia, Contrafatto Donatella, Lanzafame Salvatore, Maci Tiziana, Gambardella Antonio, Quattrone Aldo, Zappia Mario

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 Presenilin-2
Share to Alzheimer Disease
Share to Genetic Predisposition to Disease

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Lewy Body Disease

Share to Point Mutation

Source

Identifiers

PMID: 21409510
DOI: 10.1007/s10072-011-0497-4

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Presenilin-2 gene mutation presenting as Lewy body dementia?PMID 21409510Read ↗

PSEN2 Mutations May Mimic Frontotemporal Dementia: Two New Case Reports and a Systematic ReviewSemantic proximity Read ↗

Case Report of a 63-Year-Old Patient With Alzheimer Disease and a Novel Presenilin 2 Mutation.Semantic proximity Read ↗

The genetics of dementia with Lewy bodies.Semantic proximity Read ↗

A novel presenilin mutation (M233V) causing very early onset Alzheimer's disease with Lewy bodiesSemantic proximity Read ↗

Dementia with Lewy bodies: disease concept and genetics.Semantic proximity Read ↗

Presenilin-1 mutations in Alzheimer's disease.Semantic proximity Read ↗

A novel PSEN2 mutation associated with a peculiar phenotype.Semantic proximity Read ↗

Clinical aspects of hereditary frontotemporal dementia.Semantic proximity Read ↗

Atypical dementia associated with a novel presenilin-2 mutation.Semantic proximity Read ↗

Recent advances in the genetics of dementia with lewy bodies.Semantic proximity Read ↗

Variant Alzheimer disease with spastic paraparesis: a rare presenilin-1 mutation.Semantic proximity Read ↗

Clinical and biomarker changes in presymptomatic genetic frontotemporal dementiaSemantic proximity Read ↗

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