(Q36863046)

16 August 2017

1 reference

title

Frontotemporal lobar degeneration with ubiquitin-positive inclusions: a molecular genetic update (English)

1 reference

frontotemporal lobar degeneration

16 August 2017

1 reference

based on heuristic

inferred from title

author

Christine Van Broeckhoven

7

Christine Van Broeckhoven

0 references

Julie van der Zee

1

Julie van der Zee

0 references

Ilse Gijselinck

2

Ilse Gijselinck

0 references

Samir Kumar-Singh

Samir Kumar-Singh

5

0 references

Marc Cruts

6

Marc Cruts

1 reference

16 August 2017

Daniel Pirici

3

1 reference

PubMed ID

17596717

16 August 2017

Daniel Pirici

4

1 reference

16 August 2017

1 January 2007

1 reference

Neurodegenerative Diseases

16 August 2017

1 reference

16 August 2017

4

1 reference

16 August 2017

2-3

1 reference

16 August 2017

227-235

1 reference

Frontotemporal lobar degeneration: a consensus on clinical diagnostic criteria

16 August 2017

1 reference

The prevalence of frontotemporal dementia

21 January 2018

1 reference

The prevalence and causes of dementia in people under the age of 65 years

21 January 2018

1 reference

Frontotemporal lobar degeneration: demographic characteristics of 353 patients

21 January 2018

1 reference

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

21 January 2018

1 reference

Familial aggregation in frontotemporal dementia.

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

Hereditary dysphasic disinhibition dementia: a frontotemporal dementia linked to 17q21-22.

21 January 2018

1 reference

Familial frontotemporal dementia with ubiquitin-positive inclusions is linked to chromosome 17q21-22.

21 January 2018

1 reference

Tau negative frontal lobe dementia at 17q21: significant finemapping of the candidate region to a 4.8 cM interval.

21 January 2018

1 reference

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

21 January 2018

1 reference

A common inversion under selection in Europeans

21 January 2018

1 reference

Cellular localization of gene expression for progranulin

21 January 2018

1 reference

Familial non-specific dementia maps to chromosome 3

21 January 2018

1 reference

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

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1159/000101847

1 reference

16 August 2017

1 reference

PubMed ID

17596717