(Q33898394)

English

FTLD-TDP with motor neuron disease, visuospatial impairment and a progressive supranuclear palsy-like syndrome: broadening the clinical phenotype of TDP-43 proteinopathies. A report of three cases

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

FTLD-TDP with motor neuron disease, visuospatial impairment and a progressive supranuclear palsy-like syndrome: broadening the clinical phenotype of TDP-43 proteinopathies. A report of three cases (English)

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

motor neuron disease

1 reference

based on heuristic

inferred from title

Radoslav Matěj

8

object named as

Radoslav Matěj

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

object named as

Robert Rusina

1

0 references

Gabor G. Kovacs

object named as

Gabor G Kovacs

2

0 references

6

object named as

Iva Holmerová

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

author name string

Jindřich Fiala

3

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

Jakub Hort

4

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

Petr Ridzoň

5

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

Thomas Ströbel

7

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

publication date

10 May 2011

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

11

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

50

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

https://scigraph.springernature.com/pub.10.1186/1471-2377-11-50

0 references

Cognitive impairment in patients with multiple system atrophy and progressive supranuclear palsy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3112085

5 July 2018

Sporadic corticobasal syndrome due to FTLD-TDP.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3112085

5 July 2018

Brain progranulin expression in GRN-associated frontotemporal lobar degeneration

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3112085

5 July 2018

TARDBP 3'-UTR variant in autopsy-confirmed frontotemporal lobar degeneration with TDP-43 proteinopathy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3112085

5 July 2018

Evaluation of subcortical pathology and clinical correlations in FTLD-U subtypes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3112085

5 July 2018

TARDBP mutations in motoneuron disease with frontotemporal lobar degeneration

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3112085

5 July 2018

Amyotrophic lateral sclerosis, frontotemporal dementia and beyond: the TDP-43 diseases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3112085

5 July 2018

Clinical and pathological continuum of multisystem TDP-43 proteinopathies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3112085

5 July 2018

Amyotrophic lateral sclerosis-plus syndrome with TAR DNA-binding protein-43 pathology

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3112085

5 July 2018

Frontotemporal dementia in a large Swedish family is caused by a progranulin null mutation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3112085

5 July 2018

Parietal lobe deficits in frontotemporal lobar degeneration caused by a mutation in the progranulin gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3112085

5 July 2018

Prominent phenotypic variability associated with mutations in Progranulin

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3112085

5 July 2018

Neuropathologic diagnostic and nosologic criteria for frontotemporal lobar degeneration: consensus of the Consortium for Frontotemporal Lobar Degeneration

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3112085

5 July 2018

Progranulin and frontotemporal lobar degeneration

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3112085

5 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3112085

5 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3112085

5 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3112085

5 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3112085

5 July 2018

Visuospatial functions in atypical parkinsonian syndromes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3112085

5 July 2018

El Escorial revisited: revised criteria for the diagnosis of amyotrophic lateral sclerosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3112085

5 July 2018

Frontotemporal dementia and Parkinsonism linked to chromosome 17: a new group of tauopathies.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3112085

5 July 2018

Amyotrophic lateral sclerosis with dementia showing clinical parkinsonism and severe degeneration of the substantia nigra: report of an autopsy case

1 reference

https://api.crossref.org/works/10.1186%2F1471-2377-11-50

21 January 2018

Clinical, genetic, and pathologic characteristics of patients with frontotemporal dementia and progranulin mutations.

1 reference

https://api.crossref.org/works/10.1186%2F1471-2377-11-50

21 January 2018

Frontotemporal dementia and parkinsonism associated with the IVS1+1G->A mutation in progranulin: a clinicopathologic study.

1 reference

https://api.crossref.org/works/10.1186%2F1471-2377-11-50

21 January 2018

A novel deletion in progranulin gene is associated with FTDP-17 and CBS.

1 reference

https://api.crossref.org/works/10.1186%2F1471-2377-11-50

21 January 2018

Corticobasal syndrome associated with the A9D Progranulin mutation

1 reference

https://api.crossref.org/works/10.1186%2F1471-2377-11-50

21 January 2018

Subcortical dementia revisited: similarities and differences in cognitive function between progressive supranuclear palsy (PSP), corticobasal degeneration (CBD) and multiple system atrophy (MSA).

1 reference

https://api.crossref.org/works/10.1186%2F1471-2377-11-50

21 January 2018

Neuroanatomical substrate of visuospatial and visuoperceptual impairment in Parkinson's disease.

1 reference

https://api.crossref.org/works/10.1186%2F1471-2377-11-50

21 January 2018

Selective impairment of verb processing associated with pathological changes in Brodmann areas 44 and 45 in the motor neurone disease-dementia-aphasia syndrome.

1 reference

https://api.crossref.org/works/10.1186%2F1471-2377-11-50

21 January 2018

Atypical progressive supranuclear palsy with corticospinal tract degeneration.

1 reference

https://api.crossref.org/works/10.1186%2F1471-2377-11-50

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1186%2F1471-2377-11-50

21 January 2018

Clinical characteristics of patients with frontotemporal dementia with and without lobar atrophy on MRI.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3112085

29 October 2018

SIC Task Force appraisal of clinical diagnostic criteria for parkinsonian disorders

1 reference

https://pubmed.ncbi.nlm.nih.gov/21569259

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Frontotemporal lobar degeneration with ubiquitin-only-immunoreactive neuronal changes: broadening the clinical picture to include progressive supranuclear palsy

1 reference

https://pubmed.ncbi.nlm.nih.gov/21569259

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical, imaging and pathological correlates of a hereditary deficit in verb and action processing

1 reference

https://pubmed.ncbi.nlm.nih.gov/21569259

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Severe subcortical TDP-43 pathology in sporadic frontotemporal lobar degeneration with motor neuron disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/21569259

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1186/1471-2377-11-50

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

Dimensions Publication ID

1 reference

https://scigraph.springernature.com/pub.10.1186/1471-2377-11-50

9 September 2019

Internet Archive ID

pubmed-PMC3112085

0 references

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

29 July 2017

ResearchGate publication ID

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