(Q46531828)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15940384%20AND%20SRC:MED&resulttype=core&format=json

12 January 2020

title

Familial frontotemporal dementia associated with the novel MAPT mutation T427M (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15940384%20AND%20SRC:MED&resulttype=core&format=json

12 January 2020

main subject

frontotemporal dementia

1 reference

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15940384%20AND%20SRC:MED&resulttype=core&format=json

12 January 2020

Michela Morbin

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15940384%20AND%20SRC:MED&resulttype=core&format=json

12 January 2020

Fabrizio Tagliavini

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15940384%20AND%20SRC:MED&resulttype=core&format=json

12 January 2020

Giorgio Giaccone

1

1 reference

ORCID Public Data File 2021

Giacomina Rossi

2

object named as

Giacomina Rossi

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15940384%20AND%20SRC:MED&resulttype=core&format=json

12 January 2020

9

Orso Bugiani

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15940384%20AND%20SRC:MED&resulttype=core&format=json

12 January 2020

6

Marcella Catania

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15940384%20AND%20SRC:MED&resulttype=core&format=json

12 January 2020

4

Gabriella Marcon

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15940384%20AND%20SRC:MED&resulttype=core&format=json

12 January 2020

3

Laura Farina

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15940384%20AND%20SRC:MED&resulttype=core&format=json

12 January 2020

author name string

Leonardo Sacco

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15940384%20AND%20SRC:MED&resulttype=core&format=json

12 January 2020

publication date

6 June 2005

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15940384%20AND%20SRC:MED&resulttype=core&format=json

12 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15940384%20AND%20SRC:MED&resulttype=core&format=json

12 January 2020

volume

252

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15940384%20AND%20SRC:MED&resulttype=core&format=json

12 January 2020

issue

12

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15940384%20AND%20SRC:MED&resulttype=core&format=json

12 January 2020

page(s)

1543-1545

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15940384%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1007/s00415-005-0879-8

12 January 2020

exact match

0 references

cites work

Frontotemporal lobar degeneration: a consensus on clinical diagnostic criteria

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00415-005-0879-8

Tau gene mutation G389R causes a tauopathy with abundant pick body-like inclusions and axonal deposits.

21 January 2018

1 reference

12 December 2020

Autosomal dominant dementia with widespread neurofibrillary tangles.

1 reference

12 December 2020

Mutation in the tau gene in familial multiple system tauopathy with presenile dementia

1 reference

12 December 2020

Association of missense and 5'-splice-site mutations in tau with the inherited dementia FTDP-17

1 reference

12 December 2020

The tau R406W mutation causes progressive presenile dementia with bitemporal atrophy

1 reference

12 December 2020

Frontotemporal dementia and parkinsonism linked to chromosome 17: a consensus conference. Conference Participants

1 reference

12 December 2020

A neuropsychological instrument adding to the description of patients with suspected cortical dementia: the Milan overall dementia assessment

1 reference

12 December 2020

Phenotypic variation in hereditary frontotemporal dementia with tau mutations.

1 reference

12 December 2020

Tau is a candidate gene for chromosome 17 frontotemporal dementia

1 reference

12 December 2020

10.1007/S00415-005-0879-8

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15940384%20AND%20SRC:MED&resulttype=core&format=json

release_qdmdy2kkcnfyzgyuflasbe73ua

12 January 2020

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/qdmdy2kkcnfyzgyuflasbe73ua

24 November 2022

mapped directly with Wikidata item

1 reference