(Q59698065)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18157829%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

title

Progranulin locus deletion in frontotemporal dementia (English)

1 reference

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31 December 2019

main subject

dementia

0 references

frontotemporal dementia

1 reference

4

1 reference

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31 December 2019

author name string

Gijselinck I

1

1 reference

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31 December 2019

van der Zee J

2

1 reference

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31 December 2019

Engelborghs S

3

1 reference

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31 December 2019

Peeters K

5

1 reference

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31 December 2019

Mattheijssens M

6

1 reference

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31 December 2019

Corsmit E

7

1 reference

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31 December 2019

Del-Favero J

8

1 reference

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31 December 2019

De Deyn PP

9

1 reference

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31 December 2019

Van Broeckhoven C

10

1 reference

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31 December 2019

Cruts M

11

1 reference

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31 December 2019

publication date

1 January 2008

1 reference

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31 December 2019

1 reference

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31 December 2019

volume

29

1 reference

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31 December 2019

issue

1

1 reference

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31 December 2019

page(s)

53-58

1 reference

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

31 December 2019

cites work

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20651

7 January 2021

Neuropathologic heterogeneity in HDDD1: a familial frontotemporal lobar degeneration with ubiquitin-positive inclusions and progranulin mutation.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20651

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20651

7 January 2021

Progranulin mutations in Dutch familial frontotemporal lobar degeneration

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20651

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20651

7 January 2021

The Middelheim Frontality Score: a behavioural assessment scale that discriminates frontotemporal dementia from Alzheimer's disease.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20651

7 January 2021

Prospective Belgian study of neurodegenerative and vascular dementia: APOE genotype effects

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20651

7 January 2021

Frontotemporal dementia: clinicopathological correlations

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20651

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20651

7 January 2021

Characteristics of frontotemporal dementia patients with a Progranulin mutation

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20651

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20651

7 January 2021

Progranulin null mutations in both sporadic and familial frontotemporal dementia

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20651

7 January 2021

A novel progranulin mutation associated with variable clinical presentation and tau, TDP43 and alpha-synuclein pathology.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20651

7 January 2021

Late-onset frontotemporal dementia associated with a novel PGRN mutation.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20651

7 January 2021

Novel splicing mutation in the progranulin gene causing familial corticobasal syndrome.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20651

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20651

7 January 2021

Progranulin mutations in primary progressive aphasia: the PPA1 and PPA3 families.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20651

7 January 2021

Frontotemporal lobar degeneration: a consensus on clinical diagnostic criteria

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20651

7 January 2021

Mutations in progranulin explain atypical phenotypes with variants in MAPT.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20651

7 January 2021

Tau is a candidate gene for chromosome 17 frontotemporal dementia

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20651

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20651

7 January 2021

The prevalence of frontotemporal dementia

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20651

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20651

7 January 2021

Implications of human genome architecture for rearrangement-based disorders: the genomic basis of disease

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20651

7 January 2021

APP duplication is sufficient to cause early onset Alzheimer's dementia with cerebral amyloid angiopathy

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20651

7 January 2021

Clinicopathologic features of frontotemporal dementia with progranulin sequence variation.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20651

7 January 2021

Familial aggregation in frontotemporal dementia.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20651

7 January 2021

Microdeletions involving the SCN1A gene may be common in SCN1A-mutation-negative SMEI patients.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20651

7 January 2021

A comprehensive analysis of common copy-number variations in the human genome

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.20651

7 January 2021

Identifiers

DOI

10.1002/HUMU.20651

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:18157829%20AND%20SRC:MED&resulttype=core&format=json

31 December 2019

1 reference