(Q48946574)

English

Clinical course of patients with familial early-onset Alzheimer's disease potentially lacking senile plaques bearing the E693Δ mutation in amyloid precursor protein.

scientific article published on 13 August 2011

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scholarly article

1 reference

Europe PubMed Central

17 February 2018

http://europepmc.org/abstract/MED/21846988

Clinical course of patients with familial early-onset Alzheimer's disease potentially lacking senile plaques bearing the E693Δ mutation in amyloid precursor protein. (English)

1 reference

Europe PubMed Central

17 February 2018

http://europepmc.org/abstract/MED/21846988

Alzheimer's disease

0 references

early-onset Alzheimer's disease

1 reference

based on heuristic

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author name string

Hiroyuki Shimada

1

1 reference

Europe PubMed Central

17 February 2018

http://europepmc.org/abstract/MED/21846988

Suzuka Ataka

2

1 reference

Europe PubMed Central

17 February 2018

http://europepmc.org/abstract/MED/21846988

Takami Tomiyama

3

1 reference

Europe PubMed Central

17 February 2018

http://europepmc.org/abstract/MED/21846988

Hajime Takechi

4

1 reference

Europe PubMed Central

17 February 2018

http://europepmc.org/abstract/MED/21846988

Hiroshi Mori

5

1 reference

Europe PubMed Central

17 February 2018

http://europepmc.org/abstract/MED/21846988

Takami Miki

6

1 reference

Europe PubMed Central

17 February 2018

http://europepmc.org/abstract/MED/21846988

publication date

13 August 2011

1 reference

Europe PubMed Central

17 February 2018

http://europepmc.org/abstract/MED/21846988

Dementia and Geriatric Cognitive Disorders

1 reference

Europe PubMed Central

17 February 2018

http://europepmc.org/abstract/MED/21846988

32

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Europe PubMed Central

17 February 2018

http://europepmc.org/abstract/MED/21846988

1

1 reference

Europe PubMed Central

17 February 2018

http://europepmc.org/abstract/MED/21846988

45-54

1 reference

Europe PubMed Central

17 February 2018

http://europepmc.org/abstract/MED/21846988

Alzheimer's disease is a synaptic failure

1 reference

https://api.crossref.org/works/10.1159%2F000330017

21 January 2018

Natural oligomers of the amyloid-beta protein specifically disrupt cognitive function

1 reference

https://api.crossref.org/works/10.1159%2F000330017

21 January 2018

A specific amyloid-beta protein assembly in the brain impairs memory

1 reference

https://api.crossref.org/works/10.1159%2F000330017

21 January 2018

A Oligomer-Induced Aberrations in Synapse Composition, Shape, and Density Provide a Molecular Basis for Loss of Connectivity in Alzheimer's Disease

1 reference

https://api.crossref.org/works/10.1159%2F000330017

21 January 2018

Natural oligomers of the Alzheimer amyloid-beta protein induce reversible synapse loss by modulating an NMDA-type glutamate receptor-dependent signaling pathway

1 reference

https://api.crossref.org/works/10.1159%2F000330017

21 January 2018

Is Alzheimer's disease a result of presynaptic failure? Synaptic dysfunctions induced by oligomeric beta-amyloid

1 reference

https://api.crossref.org/works/10.1159%2F000330017

21 January 2018

A new amyloid beta variant favoring oligomerization in Alzheimer's-type dementia.

1 reference

https://api.crossref.org/works/10.1159%2F000330017

21 January 2018

Kinetic modeling of amyloid binding in humans using PET imaging and Pittsburgh Compound-B.

1 reference

https://api.crossref.org/works/10.1159%2F000330017

21 January 2018

Quantitative and qualitative analyses of clock drawings in Alzheimer's and Huntington's disease

1 reference

https://api.crossref.org/works/10.1159%2F000330017

21 January 2018

MRI and CSF biomarkers in normal, MCI, and AD subjects: diagnostic discrimination and cognitive correlations

1 reference

https://api.crossref.org/works/10.1159%2F000330017

21 January 2018

Cerebrospinal fluid tau in dementia disorders: a large scale multicenter study by a Japanese study group.

1 reference

https://api.crossref.org/works/10.1159%2F000330017

21 January 2018

A novel presenilin-1 mutation (Leu85Pro) in early-onset Alzheimer disease with spastic paraparesis.

1 reference

https://api.crossref.org/works/10.1159%2F000330017

21 January 2018

Hereditary dentatorubral-pallidoluysian atrophy

1 reference

https://api.crossref.org/works/10.1159%2F000330017

21 January 2018

Early onset autosomal dominant dementia with ataxia, extrapyramidal features, and epilepsy

1 reference

https://api.crossref.org/works/10.1159%2F000330017

21 January 2018

Clinical features and neuropathology of autosomal dominant spinocerebellar ataxia (SCA17).

1 reference

https://api.crossref.org/works/10.1159%2F000330017

21 January 2018

Autosomal dominant cerebellar ataxia: frequency analysis and clinical characterization of 45 families from Portugal.

1 reference

https://api.crossref.org/works/10.1159%2F000330017

21 January 2018

A mouse model of amyloid beta oligomers: their contribution to synaptic alteration, abnormal tau phosphorylation, glial activation, and neuronal loss in vivo.

1 reference

https://api.crossref.org/works/10.1159%2F000330017

21 January 2018

Identifiers

10.1159/000330017

1 reference

Europe PubMed Central

17 February 2018

http://europepmc.org/abstract/MED/21846988

1 reference

Europe PubMed Central

17 February 2018

http://europepmc.org/abstract/MED/21846988

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