(Q48321987)

10 February 2018

reason for preferred rank

title

Phenotypic presentation of frontotemporal dementia with Parkinsonism‐chromosome 17 type P301S in a patient of Jewish‐Algerian origin (English)

1 reference

29 December 2023

Phenotypic presentation of frontotemporal dementia with Parkinsonism-chromosome 17 type P301S in a patient of Jewish-Algerian origin (English)

1 reference

PubMed ID

12722177

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A12722177

29 December 2023

0 references

1 reference

frontotemporal dementia

1 reference

1 reference

29 December 2023

author name string

Edith Werber

1

1 reference

10 February 2018

Colin Klein

2

1 reference

10 February 2018

Jonathan Grünfeld

3

1 reference

10 February 2018

José Martin Rabey

4

1 reference

10 February 2018

language of work or name

English

0 references

publication date

1 May 2003

1 reference

10 February 2018

full work available at URL

https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fmds.10401

1 reference

https://onlinelibrary.wiley.com/doi/full/10.1002/mds.10401

29 December 2023

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29 December 2023

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10 February 2018

volume

18

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10 February 2018

issue

5

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10 February 2018

page(s)

595-598

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10 February 2018

Clinical characteristics of a family with chromosome 17-linked disinhibition-dementia-parkinsonism-amyotrophy complex.

cites work

1 reference

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

21 January 2018

1 reference

Tau protein pathology in neurodegenerative diseases.

21 January 2018

1 reference

A clinical pathological comparison of three families with frontotemporal dementia and identical mutations in the tau gene (P301L)

21 January 2018

1 reference

Tau pathology in a family with dementia and a P301L mutation in tau.

21 January 2018

1 reference

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

21 January 2018

1 reference

Mutation-specific functional impairments in distinct tau isoforms of hereditary FTDP-17.

21 January 2018

1 reference

Inherited frontotemporal dementia in nine British families associated with intronic mutations in the tau gene.

21 January 2018

1 reference

The genetic and pathological classification of familial frontotemporal dementia.

21 January 2018

1 reference

Tau is a candidate gene for chromosome 17 frontotemporal dementia

21 January 2018

1 reference

Rapidly progressive autosomal dominant parkinsonism and dementia with pallido-ponto-nigral degeneration

21 January 2018

1 reference

From genotype to phenotype: a clinical pathological, and biochemical investigation of frontotemporal dementia and parkinsonism (FTDP-17) caused by the P301L tau mutation.

21 January 2018

1 reference

Phenotypic correlations in FTDP-17.

21 January 2018

1 reference

FTDP-17: an early-onset phenotype with parkinsonism and epileptic seizures caused by a novel mutation

21 January 2018

1 reference

A Japanese patient with frontotemporal dementia and parkinsonism by a tau P301S mutation

21 January 2018

1 reference

Localization of the gene for rapidly progressive autosomal dominant parkinsonism and dementia with pallido-ponto-nigral degeneration to chromosome 17q21

21 January 2018

1 reference

Positron emission tomography in pallido-ponto-nigral degeneration (PPND) family (frontotemporal dementia with parkinsonism linked to chromosome 17 and point mutation in tau gene)

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1002/MDS.10401

1 reference

10 February 2018

PubMed ID

12722177

1 reference

10 February 2018