(Q32061209)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11220749%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

title

Familial atypical progressive supranuclear palsy associated with homozigosity for the delN296 mutation in the tau gene (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11220749%20AND%20SRC:MED&resulttype=core&format=json

progressive supranuclear palsy

4 November 2019

main subject

1 reference

based on heuristic

inferred from title

author

Cristóbal Carnero Pardo

3

1 reference

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4 November 2019

author name string

P Pastor

1

1 reference

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4 November 2019

E Pastor

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11220749%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

R Vela

4

1 reference

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4 November 2019

T García

5

1 reference

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4 November 2019

G Amer

6

1 reference

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4 November 2019

E Tolosa

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11220749%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

R Oliva

8

1 reference

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4 November 2019

publication date

1 February 2001

1 reference

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4 November 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11220749%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

volume

49

1 reference

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4 November 2019

page(s)

263-267

1 reference

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4 November 2019

issue

2

1 reference

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Tau protein pathology in neurodegenerative diseases.

4 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1002%2F1531-8249%2820010201%2949%3A2%3C263%3A%3AAID-ANA50%3E3.0.CO%3B2-K

Frontotemporal dementia and parkinsonism linked to chromosome 17: a consensus conference. Conference Participants

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1531-8249%2820010201%2949%3A2%3C263%3A%3AAID-ANA50%3E3.0.CO%3B2-K

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1531-8249%2820010201%2949%3A2%3C263%3A%3AAID-ANA50%3E3.0.CO%3B2-K

Familial multiple system tauopathy with presenile dementia: a disease with abundant neuronal and glial tau filaments

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1531-8249%2820010201%2949%3A2%3C263%3A%3AAID-ANA50%3E3.0.CO%3B2-K

Mutation in the tau gene in familial multiple system tauopathy with presenile dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1531-8249%2820010201%2949%3A2%3C263%3A%3AAID-ANA50%3E3.0.CO%3B2-K

A mutation at codon 279 (N279K) in exon 10 of the Tau gene causes a tauopathy with dementia and supranuclear palsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1531-8249%2820010201%2949%3A2%3C263%3A%3AAID-ANA50%3E3.0.CO%3B2-K

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.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1531-8249%2820010201%2949%3A2%3C263%3A%3AAID-ANA50%3E3.0.CO%3B2-K

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1531-8249%2820010201%2949%3A2%3C263%3A%3AAID-ANA50%3E3.0.CO%3B2-K

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1531-8249%2820010201%2949%3A2%3C263%3A%3AAID-ANA50%3E3.0.CO%3B2-K

Identification of a novel microtubule binding and assembly domain in the developmentally regulated inter-repeat region of tau.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1531-8249%2820010201%2949%3A2%3C263%3A%3AAID-ANA50%3E3.0.CO%3B2-K

Untangling tau-related dementia

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1531-8249%2820010201%2949%3A2%3C263%3A%3AAID-ANA50%3E3.0.CO%3B2-K

A mutation in the microtubule-associated protein tau in pallido-nigro-luysian degeneration.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1531-8249%2820010201%2949%3A2%3C263%3A%3AAID-ANA50%3E3.0.CO%3B2-K

Progressive supranuclear palsy-like syndrome in two siblings of a consanguineous marriage

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1531-8249%2820010201%2949%3A2%3C263%3A%3AAID-ANA50%3E3.0.CO%3B2-K

Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1531-8249%2820010201%2949%3A2%3C263%3A%3AAID-ANA50%3E3.0.CO%3B2-K

Fast and sensitive silver staining of DNA in polyacrylamide gels

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1531-8249%2820010201%2949%3A2%3C263%3A%3AAID-ANA50%3E3.0.CO%3B2-K

Determinants of 4-repeat tau expression. Coordination between enhancing and inhibitory splicing sequences for exon 10 inclusion

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1531-8249%2820010201%2949%3A2%3C263%3A%3AAID-ANA50%3E3.0.CO%3B2-K

Progressive apraxia in clinically discordant monozygotic twins

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1531-8249%2820010201%2949%3A2%3C263%3A%3AAID-ANA50%3E3.0.CO%3B2-K

Amyotrophic lateral sclerosis associated with homozygosity for an Asp90Ala mutation in CuZn-superoxide dismutase

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F1531-8249%2820010201%2949%3A2%3C263%3A%3AAID-ANA50%3E3.0.CO%3B2-K

10.1002/1531-8249(20010201)49:2<263::AID-ANA50>3.0.CO;2-K

21 January 2018

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11220749%20AND%20SRC:MED&resulttype=core&format=json

4 November 2019

1 reference