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

A novel presenilin mutation (M233V) causing very early onset Alzheimer's disease with Lewy bodies

1 Nov 2001

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 Alzheimer's disease research and treatments
Share to Cholinesterase and Neurodegenerative Diseases
Share to Mitochondrial Function and Pathology

Source

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Identifiers

PMID: 11684347
DOI: 10.1016/s0304-3940(01)02254-6

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A novel presenilin mutation (M233V) causing very early onset Alzheimer's disease with Lewy bodiesPMID 11684347Read ↗

Very early onset AD with a de novo mutation in the presenilin 1 gene (Met 233 Leu).Semantic proximity Read ↗

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

New V272A presenilin 1 mutation with very early onset subcortical dementia and parkinsonismSemantic proximity Read ↗

Clinical features of early-onset Alzheimer disease in a large kindred with an E280A presenilin-1 mutationSemantic proximity Read ↗

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

Presenilin-2 gene mutation presenting as Lewy body dementia?Semantic proximity Read ↗

The R269H mutation in presenilin-1 presenting as late-onset autosomal dominant Alzheimer's diseaseSemantic proximity Read ↗

[Alzheimer's disease due to presenilin mutations].Semantic proximity Read ↗

Novel presenilin 1 mutation (S170F) causing Alzheimer disease with Lewy bodies in the third decade of life.Semantic proximity Read ↗

A novel PSEN1 gene mutation (L235R) associated with familial early-onset Alzheimer's disease.Semantic proximity Read ↗

A novel presenilin 1 mutation (Leu418Trp) associated with spasticity, parkinsonism, and white matter lesion in a dominant Alzheimer's family.Semantic proximity Read ↗

A presenilin 1 mutation in the first case of Alzheimer's disease.Semantic proximity Read ↗

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