(Q48959566)

English

Atypical presentation of a novel Presenilin 1 R377W mutation: sporadic, late-onset Alzheimer disease with epilepsy and frontotemporal atrophy

scientific article published on 6 August 2011

In more languages

default for all languages

No label defined

No description defined

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

17 February 2018

http://europepmc.org/abstract/MED/21822699

Atypical presentation of a novel Presenilin 1 R377W mutation: sporadic, late-onset Alzheimer disease with epilepsy and frontotemporal atrophy (English)

1 reference

Europe PubMed Central

PubMed publication ID

17 February 2018

http://europepmc.org/abstract/MED/21822699

Alzheimer's disease

0 references

2

1 reference

Europe PubMed Central

PubMed publication ID

17 February 2018

http://europepmc.org/abstract/MED/21822699

Cristian Bonvicini

3

1 reference

Europe PubMed Central

PubMed publication ID

17 February 2018

http://europepmc.org/abstract/MED/21822699

Massimo Gennarelli

object named as

Massimo Gennarelli

7

0 references

Barbara Borroni

1

object named as

Barbara Borroni

1 reference

Europe PubMed Central

PubMed publication ID

17 February 2018

Alessandro Padovani

8

object named as

Alessandro Padovani

1 reference

Europe PubMed Central

PubMed publication ID

17 February 2018

http://europepmc.org/abstract/MED/21822699

author name string

Silvana Archetti

4

1 reference

Europe PubMed Central

PubMed publication ID

17 February 2018

http://europepmc.org/abstract/MED/21822699

Antonella Alberici

5

1 reference

Europe PubMed Central

PubMed publication ID

17 February 2018

http://europepmc.org/abstract/MED/21822699

Andrea Lupi

6

1 reference

Europe PubMed Central

PubMed publication ID

17 February 2018

http://europepmc.org/abstract/MED/21822699

publication date

6 August 2011

1 reference

Europe PubMed Central

PubMed publication ID

17 February 2018

http://europepmc.org/abstract/MED/21822699

Neurological Sciences

1 reference

Europe PubMed Central

PubMed publication ID

17 February 2018

http://europepmc.org/abstract/MED/21822699

33

1 reference

Europe PubMed Central

PubMed publication ID

17 February 2018

http://europepmc.org/abstract/MED/21822699

2

1 reference

Europe PubMed Central

PubMed publication ID

17 February 2018

http://europepmc.org/abstract/MED/21822699

375-378

1 reference

Europe PubMed Central

PubMed publication ID

17 February 2018

http://europepmc.org/abstract/MED/21822699

Genotype-phenotype relationships of presenilin-1 mutations in Alzheimer's disease: an update

1 reference

https://api.crossref.org/works/10.1007%2FS10072-011-0714-1

21 January 2018

Wide Range of Disease Onset in a Family With Alzheimer Disease and a His163Tyr Mutation in the Presenilin-1 Gene

1 reference

https://api.crossref.org/works/10.1007%2FS10072-011-0714-1

21 January 2018

Early-onset Alzheimer's disease with a de novo mutation in the presenilin 1 gene

1 reference

https://api.crossref.org/works/10.1007%2FS10072-011-0714-1

21 January 2018

Presenilin 1 mutation in an african american family presenting with atypical Alzheimer dementia

1 reference

https://api.crossref.org/works/10.1007%2FS10072-011-0714-1

21 January 2018

The impact of different presenilin 1 andpresenilin 2 mutations on amyloid deposition, neurofibrillary changes and neuronal loss in the familial Alzheimer's disease brain: evidence for other phenotype-modifying factors

1 reference

https://api.crossref.org/works/10.1007%2FS10072-011-0714-1

21 January 2018

Amyloid angiopathy and variability in amyloid beta deposition is determined by mutation position in presenilin-1-linked Alzheimer's disease

1 reference

https://api.crossref.org/works/10.1007%2FS10072-011-0714-1

21 January 2018

Early‐onset Alzheimer's disease with presenilin‐1 M139V mutation: clinical, neuropsychological and neuropathological study

1 reference

https://api.crossref.org/works/10.1007%2FS10072-011-0714-1

21 January 2018

Early onset familial Alzheimer's disease: Mutation frequency in 31 families.

1 reference

https://api.crossref.org/works/10.1007%2FS10072-011-0714-1

21 January 2018

Dementia, delusions and seizures: storage disease or genetic AD?

1 reference

https://api.crossref.org/works/10.1007%2FS10072-011-0714-1

21 January 2018

A novel Polish presenilin-1 mutation (P117L) is associated with familial Alzheimer's disease and leads to death as early as the age of 28 years.

1 reference

https://api.crossref.org/works/10.1007%2FS10072-011-0714-1

21 January 2018

Apolipoprotein E genotype and Alzheimer's disease

1 reference

https://api.crossref.org/works/10.1007%2FS10072-011-0714-1

21 January 2018

Apolipoprotein E genotype and Alzheimer's disease. Alzheimer's Disease Collaborative Group

1 reference

https://pubmed.ncbi.nlm.nih.gov/21822699

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Tau and Abeta42 in cerebrospinal fluid from healthy adults 21-93 years of age: establishment of reference values.

1 reference

https://pubmed.ncbi.nlm.nih.gov/21822699

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S10072-011-0714-1

1 reference

Europe PubMed Central

PubMed publication ID

17 February 2018

http://europepmc.org/abstract/MED/21822699

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

17 February 2018

http://europepmc.org/abstract/MED/21822699

ResearchGate publication ID

0 references

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q48959566&oldid=2263641567"