Frontotemporal dementia-like phenotypes associated with presenilin-1 mutations

scientific article published on August 2006

Frontotemporal dementia-like phenotypes associated with presenilin-1 mutations is …
instance of (P31):
scholarly articleQ13442814
review articleQ7318358

External links are
P356DOI10.1177/1533317506290448
P698PubMed publication ID16948293

P2093author name stringMario F Mendez
Aaron McMurtray
P2860cites work“Mini-mental state”Q25938989
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Forebrain degeneration and ventricle enlargement caused by double knockout of Alzheimer's presenilin-1 and presenilin-2Q28511413
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Tau suppression in a neurodegenerative mouse model improves memory functionQ29615831
Neuropathologic, biochemical, and molecular characterization of the frontotemporal dementiasQ30989766
A novel mutation (V89L) in the presenilin 1 gene in a family with early onset Alzheimer's disease and marked behavioural disturbances.Q35465346
Tau is central in the genetic Alzheimer-frontotemporal dementia spectrumQ36284713
Chromosome 14 familial Alzheimer's disease: the clinical and neuropathological characteristics of a family with a leucine-->serine (L250S) substitution at codon 250 of the presenilin 1 geneQ36317683
Atypical dementia associated with a novel presenilin-2 mutationQ40542342
Screening for PS1 mutations in a referral-based series of AD cases: 21 novel mutationsQ40689416
A case of combined Pick's disease and Alzheimer's diseaseQ42581701
Familial frontotemporal dementia associated with a novel presenilin-1 mutationQ44020083
Pick bodies in a family with presenilin-1 Alzheimer's diseaseQ45204462
A novel presenilin 1 mutation associated with Pick's disease but not beta-amyloid plaquesQ47661255
Presenilin mutations associated with fronto-temporal dementiaQ47661266
Very early onset AD with a de novo mutation in the presenilin 1 gene (Met 233 Leu)Q48160810
Presenilin 1 mutation in an african american family presenting with atypical Alzheimer dementiaQ48279370
Tangles and neurodegenerative disease--a surprising twistQ48716151
The clinical phenotype of two missense mutations in the presenilin I gene in Japanese patientsQ48841578
A presenilin-1 mutation (Leu392Pro) in a familial AD kindred with psychiatric symptoms at onset.Q53239111
Variable phenotype of Alzheimer's disease with spastic paraparesis.Q53240458
A presenilin 1 R278I mutation presenting with language impairment.Q53265431
The Consortium to Establish a Registry for Alzheimer's Disease (CERAD). Part V. A normative study of the neuropsychological battery.Q53316862
Linkage to chromosome 14q in Alzheimer's disease (AD) patients without psychotic symptoms.Q53366990
A presenilin 1 mutation associated with familial frontotemporal dementia inhibits gamma-secretase cleavage of APP and notch.Q55473632
P433issue4
P407language of work or nameEnglishQ1860
P921main subjectfrontotemporal dementiaQ18592
P304page(s)281-286
P577publication date2006-08-01
P1433published inAmerican Journal of Alzheimer's Disease & Other DementiasQ4744232
P1476titleFrontotemporal dementia-like phenotypes associated with presenilin-1 mutations
P478volume21

Reverse relations

cites work (P2860)
Q36380671Alzheimer's disease-causing proline substitutions lead to presenilin 1 aggregation and malfunction.
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