(Q34020227)

30 July 2017

Nomenclature and nosology for neuropathologic subtypes of frontotemporal lobar degeneration: an update (English)

1 reference

frontotemporal lobar degeneration

30 July 2017

1 reference

19

1 reference

30 July 2017

Samir Kumar-Singh

15

0 references

Jillian J. Kril

Jillian Kril

6

0 references

Paul Ince

Paul G Ince

11

0 references

Gabor G. Kovacs

Gabor G Kovacs

7

0 references

Glenda Halliday

Glenda Halliday

9

0 references

John Q. Trojanowski

20

John Q Trojanowski

1 reference

30 July 2017

2

Manuela Neumann

1 reference

30 July 2017

4

Nigel J Cairns

1 reference

30 July 2017

8

Bernardino Ghetti

1 reference

30 July 2017

16

Haruhiko Akiyama

1 reference

30 July 2017

3

Eileen H Bigio

1 reference

30 July 2017

17

Atik Baborie

1 reference

30 July 2017

5

Irina Alafuzoff

1 reference

30 July 2017

12

Wouter Kamphorst

1 reference

30 July 2017

Annemieke J M Rozemuller

14

Annemieke J M Rozemuller

1 reference

30 July 2017

Ian R A Mackenzie

1

1 reference

30 July 2017

Ida E Holm

10

1 reference

30 July 2017

Tamas Revesz

13

1 reference

30 July 2017

Salvatore Spina

18

1 reference

30 July 2017

David M A Mann

21

1 reference

30 July 2017

19 November 2009

1 reference

30 July 2017

Acta Neuropathologica

1 reference

30 July 2017

119

1 reference

30 July 2017

1-4

1 reference

30 July 2017

1

1 reference

https://scigraph.springernature.com/pub.10.1007/s00401-009-0612-2

30 July 2017

0 references

cites work

FUS pathology in basophilic inclusion body disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2799633

Analysis of FUS gene mutation in familial amyotrophic lateral sclerosis within an Italian cohort

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2799633

A new subtype of frontotemporal lobar degeneration with FUS pathology

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2799633

Abundant FUS-immunoreactive pathology in neuronal intermediate filament inclusion disease

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2799633

Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2799633

Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2799633

The role of CHMP2B in frontotemporal dementia

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2799633

Nomenclature for neuropathologic subtypes of frontotemporal lobar degeneration: consensus recommendations

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2799633

alpha-Internexin aggregates are abundant in neuronal intermediate filament inclusion disease (NIFID) but rare in other neurodegenerative diseases

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2799633

Absence of FUS-immunoreactive pathology in frontotemporal dementia linked to chromosome 3 (FTD-3) caused by mutation in the CHMP2B gene.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2799633

TARDBP variation associated with frontotemporal dementia, supranuclear gaze palsy, and chorea.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2799633

Atypical frontotemporal lobar degeneration with ubiquitin-positive, TDP-43-negative neuronal inclusions

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2799633

A Reassessment of the Neuropathology of Frontotemporal Dementia Linked to Chromosome 3

29 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19924424

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

TDP-43-negative FTLD-U is a significant new clinico-pathological subtype of FTLD

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/19924424

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1007/S00401-009-0612-2

1 reference

Dimensions Publication ID

30 July 2017

0 references

1 reference

30 July 2017

1 reference