(Q33922335)

30 July 2017

FUS pathology defines the majority of tau- and TDP-43-negative frontotemporal lobar degeneration (English)

1 reference

frontotemporal lobar degeneration

30 July 2017

1 reference

14

1 reference

30 July 2017

Stuart Pickering-Brown

38

1 reference

Christine Van Broeckhoven

30 July 2017

31

Christine Van Broeckhoven

0 references

Julie van der Zee

27

Julie van der Zee

0 references

Sebastiaan Engelborghs

29

Sebastiaan Engelborghs

1 reference

30 July 2017

Peter Johannsen

10

0 references

Han-Xiang Deng

Han-Xiang Deng

33

0 references

Samir Kumar-Singh

Samir Kumar-Singh

28

0 references

Jillian J. Kril

Jillian J Kril

35

0 references

Myron F. Weiner

Myron F Weiner

21

0 references

David G. Munoz

David G Munoz

36

0 references

Jonathan D Rohrer

Jonathan D Rohrer

3

0 references

Glenda Halliday

Glenda M Halliday

34

0 references

Charles L White

Charles L White

20

0 references

John Q. Trojanowski

24

John Q Trojanowski

1 reference

30 July 2017

Martin N Rossor

45

0 references

Manuela Neumann

5

Manuela Neumann

1 reference

30 July 2017

15

Rosa Rademakers

1 reference

30 July 2017

18

Ronald C Petersen

1 reference

30 July 2017

25

Bruce L Miller

1 reference

30 July 2017

Elizabeth M. C. Fisher

42

Elizabeth M C Fisher

1 reference

30 July 2017

26

William W Seeley

1 reference

30 July 2017

Simon Mead

47

0 references

Neill R Graff-Radford

16

Neill R Graff-Radford

1 reference

30 July 2017

2

Keith A Josephs

1 reference

30 July 2017

32

Eileen H Bigio

1 reference

30 July 2017

1

Hazel Urwin

1 reference

30 July 2017

6

Astrid Authier

1 reference

30 July 2017

7

Harro Seelaar

1 reference

30 July 2017

8

John C Van Swieten

1 reference

30 July 2017

13

FReJA Consortium

1 reference

30 July 2017

19

Kimmo J Hatanpaa

1 reference

30 July 2017

Vivianna M Van Deerlin

23

Vivianna M Van Deerlin

1 reference

30 July 2017

30

Peter P De Deyn

1 reference

30 July 2017

46

John Collinge

1 reference

30 July 2017

48

Adrian M Isaacs

1 reference

30 July 2017

43

Janice L Holton

1 reference

30 July 2017

Ian R Mackenzie

4

1 reference

30 July 2017

Jeremy M Brown

9

1 reference

30 July 2017

Jorgen E Nielsen

11

1 reference

30 July 2017

Ida E Holm

12

1 reference

30 July 2017

Joseph E Parisi

17

1 reference

30 July 2017

Felix Geser

22

1 reference

30 July 2017

David M Mann

37

1 reference

30 July 2017

Valerie Doodeman

39

1 reference

30 July 2017

Gary Adamson

40

1 reference

30 July 2017

Shabnam Ghazi-Noori

41

1 reference

30 July 2017

Tamas Revesz

44

1 reference

30 July 2017

20 May 2010

1 reference

30 July 2017

Acta Neuropathologica

1 reference

30 July 2017

120

1 reference

30 July 2017

1

1 reference

30 July 2017

33-41

1 reference

https://scigraph.springernature.com/pub.10.1007/s00401-010-0698-6

30 July 2017

0 references

cites work

Frequency of ubiquitin and FUS-positive, TDP-43-negative frontotemporal lobar degeneration

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2887939

The heritability and genetics of frontotemporal lobar degeneration.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2887939

FUS pathology in basophilic inclusion body disease

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2887939

A new subtype of frontotemporal lobar degeneration with FUS pathology

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2887939

Abundant FUS-immunoreactive pathology in neuronal intermediate filament inclusion disease

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2887939

Rethinking ALS: the FUS about TDP-43.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2887939

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2887939

The role of CHMP2B in frontotemporal dementia

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2887939

Nomenclature for neuropathologic subtypes of frontotemporal lobar degeneration: consensus recommendations

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2887939

Pedigree with frontotemporal lobar degeneration--motor neuron disease and Tar DNA binding protein-43 positive neuropathology: genetic linkage to chromosome 9.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2887939

Phosphorylated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2887939

A distinct clinical, neuropsychological and radiological phenotype is associated with progranulin gene mutations in a large UK series

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2887939

CHMP2B C-truncating mutations in frontotemporal lobar degeneration are associated with an aberrant endosomal phenotype in vitro

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2887939

TDP-43 in familial and sporadic frontotemporal lobar degeneration with ubiquitin inclusions

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2887939

TDP-43 pathology in familial frontotemporal dementia and motor neuron disease without Progranulin mutations

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2887939

An autopsy case of frontotemporal dementia with severe dysarthria and motor neuron disease showing numerous basophilic inclusions

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2887939

Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2887939

Heterogeneity of ubiquitin pathology in frontotemporal lobar degeneration: classification and relation to clinical phenotype

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2887939

Pathological heterogeneity of frontotemporal lobar degeneration with ubiquitin-positive inclusions delineated by ubiquitin immunohistochemistry and novel monoclonal antibodies

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2887939

Mutations in progranulin are a major cause of ubiquitin-positive frontotemporal lobar degeneration

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2887939

Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2887939

Histopathological changes underlying frontotemporal lobar degeneration with clinicopathological correlation

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2887939

Mutations in the endosomal ESCRTIII-complex subunit CHMP2B in frontotemporal dementia

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2887939

Clinical and neuropathologic variation in neuronal intermediate filament inclusion disease

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2887939

The role of tau (MAPT) in frontotemporal dementia and related tauopathies

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2887939

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2887939

Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2887939

Neurofilament inclusion body disease: a new proteinopathy?

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2887939

Frontotemporal dementia in The Netherlands: patient characteristics and prevalence estimates from a population-based study.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2887939

Clinical and pathological diagnosis of frontotemporal dementia: report of the Work Group on Frontotemporal Dementia and Pick's Disease

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2887939

Distribution of basal ganglia lesions in generalized variant of Pick's disease: a clinicopathological study of four autopsy cases.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2887939

Neuropathological discrepancy between Japanese Pick's disease without Pick bodies and frontal lobe degeneration type of frontotemporal dementia proposed by Lund and Manchester Group.

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2887939

Inheritance of frontotemporal dementia

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2887939

Frontotemporal lobar degeneration: a consensus on clinical diagnostic criteria

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2887939

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

28 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2887939

Characterization of ubiquitinated intraneuronal inclusions in a novel Belgian frontotemporal lobar degeneration family.

28 July 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00401-010-0698-6

Distribution of cerebral cortical lesions in Pick's disease with Pick bodies: a clinicopathological study of six autopsy cases showing unusual clinical presentations.

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00401-010-0698-6

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

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2887939

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

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2887939

FUS-immunoreactive intranuclear inclusions in neurodegenerative disease.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2887939

Clinical heterogeneity in 3 unrelated families linked to VCP p.Arg159His

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2887939

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

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2887939

Frontotemporal dementia linked to chromosome 3 (FTD-3)--current concepts and the detection of a previously unknown branch of the Danish FTD-3 family.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2887939

TAR DNA-binding protein 43 immunohistochemistry reveals extensive neuritic pathology in FTLD-U: a midwest-southwest consortium for FTLD study

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2887939

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=2887939

Loss of progranulin function in frontotemporal lobar degeneration

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2887939

Basophilic inclusion body disease and neuronal intermediate filament inclusion disease: a comparative clinicopathological study

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2887939

Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2887939

Valosin-containing protein gene mutations: clinical and neuropathologic features.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2887939

Frontotemporal lobar degeneration with motor neuron disease-type inclusions predominates in 76 cases of frontotemporal degeneration.

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2887939

Classic and generalized variants of Pick's disease: A clinicopathological, ultrastructural, and immunocytochemical comparative study

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2887939

Frontotemporal lobar degeneration with ubiquitin-positive, but TDP-43-negative 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=2887939

Frontotemporal lobar degeneration and ubiquitin immunohistochemistry

29 October 2018

1 reference

12 December 2020

Frequency oftau mutations in three series of non-Alzheimer's degenerative dementia

1 reference

12 December 2020

Frontotemporal dementia

1 reference

12 December 2020

Dementia lacking distinctive histology (DLDH) revisited

1 reference

12 December 2020

Frontotemporal dementia

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

10.1007/S00401-010-0698-6

Identifiers

DOI

1 reference

Dimensions Publication ID

30 July 2017

0 references

1 reference

30 July 2017

1 reference