(Q36803014)

16 August 2017

Phenotypic variation of autosomal-dominant corticobasal degeneration (English)

1 reference

corticobasal degeneration

16 August 2017

1 reference

based on heuristic

inferred from title

author

Christine Van Broeckhoven

8

Christine Van Broeckhoven

0 references

Markus Tolnay

10

Markus Tolnay

0 references

Johannes Streffer

Johannes Streffer

3

0 references

Adriano Aguzzi

Adriano Aguzzi

9

0 references

Maria Grazia Spillantini

5

Maria Grazia Spillantini

1 reference

16 August 2017

7

Peter Brugger

1 reference

16 August 2017

Hans H Jung

1

1 reference

16 August 2017

Juliane Bremer

2

1 reference

16 August 2017

Kanwar Virdee

4

1 reference

16 August 2017

R Anthony Crowther

6

1 reference

16 August 2017

Markus Tolnay

10

1 reference

16 August 2017

18 January 2012

1 reference

16 August 2017

1 reference

16 August 2017

67

1 reference

16 August 2017

3

1 reference

16 August 2017

142-150

1 reference

The spectrum of mutations in progranulin: a collaborative study screening 545 cases of neurodegeneration

16 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3638994

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3638994

Progressive supranuclear palsy: clinicopathological concepts and diagnostic challenges

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3638994

Are frontotemporal lobar degeneration, progressive supranuclear palsy and corticobasal degeneration distinct diseases?

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3638994

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3638994

Clinical and pathologic evidence of corticobasal degeneration and progressive supranuclear palsy in familial tauopathy

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3638994

Argyrophilic grain disease: a late-onset dementia with distinctive features among tauopathies

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3638994

Mutations causing neurodegenerative tauopathies

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3638994

Corticobasal degeneration and its relationship to progressive supranuclear palsy and frontotemporal dementia

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3638994

Mutations of the prion protein gene phenotypic spectrum

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3638994

Sequence analysis of tau in familial and sporadic progressive supranuclear palsy.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3638994

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

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3638994

Neurodegenerative tauopathies

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3638994

The corticobasal degeneration syndrome overlaps progressive aphasia and frontotemporal dementia

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3638994

Clinical features differentiating patients with postmortem confirmed progressive supranuclear palsy and corticobasal degeneration.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3638994

Frontotemporal dementia and corticobasal degeneration in a family with a P301S mutation in tau.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3638994

Neuropathologic overlap of progressive supranuclear palsy, Pick's disease and corticobasal degeneration

29 September 2017

2 references

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3638994

29 September 2017

https://api.crossref.org/works/10.1159%2F000334731

Multiple isoforms of human microtubule-associated protein tau: sequences and localization in neurofibrillary tangles of Alzheimer's disease

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3638994

Progressive supranuclear palsy pathology caused by a novel silent mutation in exon 10 of the tau gene: expansion of the disease phenotype caused by tau gene mutations.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3638994

Tau pathology in two Dutch families with mutations in the microtubule-binding region of tau

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3638994

Magnetic resonance imaging of corticobasal degeneration.

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3638994

Tau proteins of Alzheimer paired helical filaments: abnormal phosphorylation of all six brain isoforms

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3638994

Clinicopathologic analysis of frontotemporal and corticobasal degenerations and PSP.

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3638994

Familial autosomal dominant cortico-basal degeneration with the P301S mutation in the tau gene: an example of phenotype variability

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3638994

A new mutation of the tau gene, G303V, in early-onset familial progressive supranuclear palsy.

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3638994

Progressive supranuclear palsy and corticobasal degeneration: lumping versus splitting

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3638994

Genetic linkage of autosomal dominant progressive supranuclear palsy to 1q31.1.

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3638994

Selective neurofibrillary degeneration of the hippocampal CA2 sector is associated with four-repeat tauopathies.

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3638994

Office of Rare Diseases neuropathologic criteria for corticobasal degeneration.

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3638994

Dementia as the most common presentation of cortical-basal ganglionic degeneration.

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3638994

Association of an extended haplotype in the tau gene with progressive supranuclear palsy

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3638994

Deletions in the prion protein gene are not associated with CJD.

5 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3638994

Corticobasal degeneration and progressive supranuclear palsy share a common tau haplotype

5 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22261560

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

SIC Task Force appraisal of clinical diagnostic criteria for parkinsonian disorders

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22261560

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1159/000334731

1 reference

16 August 2017

1 reference

16 August 2017

PubMed publication ID

22261560

1 reference