(Q42525223)

1 November 2017

The G389R mutation in the MAPT gene presenting as sporadic corticobasal syndrome (English)

1 reference

1 November 2017

Corticobasal syndrome

1 reference

Claudia Ciano

6

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author name string

Giacomina Rossi

1

1 reference

1 November 2017

Cecilia Marelli

2

1 reference

1 November 2017

Laura Farina

3

1 reference

1 November 2017

Matilde Laurà

4

1 reference

1 November 2017

Anna Maria Basile

5

1 reference

1 November 2017

Fabrizio Tagliavini

7

1 reference

1 November 2017

Davide Pareyson

8

1 reference

1 November 2017

language of work or name

English

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publication date

1 April 2008

1 reference

1 November 2017

1 reference

1 November 2017

23

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1 November 2017

6

1 reference

1 November 2017

892-895

1 reference

Hereditary frontotemporal dementia caused by Tau gene mutations.

1 November 2017

1 reference

Neurodegenerative tauopathies

21 January 2018

1 reference

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

21 January 2018

1 reference

Tau is a candidate gene for chromosome 17 frontotemporal dementia

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

A novel mutation (K317M) in the MAPT gene causes FTDP and motor neuron disease.

21 January 2018

1 reference

Constant and severe involvement of Betz cells in corticobasal degeneration is not consistent with pyramidal signs: a clinicopathological study of ten autopsy cases

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1002/MDS.21970

1 reference

1 November 2017

1 reference