Clinical and genetic features of families with frontotemporal dementia and parkinsonism linked to chromosome 17 with a P301S tau mutation (Q57983257)

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scholarly article by Y. Baba et al published 23 February 2007 in Journal of Neural Transmission

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English	Clinical and genetic features of families with frontotemporal dementia and parkinsonism linked to chromosome 17 with a P301S tau mutation	scholarly article by Y. Baba et al published 23 February 2007 in Journal of Neural Transmission

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instance of

scholarly article

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title

Clinical and genetic features of families with frontotemporal dementia and parkinsonism linked to chromosome 17 with a P301S tau mutation (English)

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main subject

dementia

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Frontotemporal dementia and parkinsonism linked to chromosome 17

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Parkinson's disease

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frontotemporal dementia

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parkinsonian syndrome

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author

Zbigniew K Wszolek

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16

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Z. K. Wszolek

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Matthew J. Farrer

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13

object named as

M. J. Farrer

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author name string

Y. Baba

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1

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M. C. Baker

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2

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I. Le Ber

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3

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A. Brice

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4

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L. Maeck

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5

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J. Kohlhase

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6

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M. Yasuda

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7

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G. Stoppe

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8

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O. Bugiani

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9

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A. D. Sperfeld

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10

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Y. Tsuboi

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11

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R. J. Uitti

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12

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B. Ghetti

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14

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M. L. Hutton

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15

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publication date

23 February 2007

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number of pages

4

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published in

Journal of Neural Transmission

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volume

114

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issue

7

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page(s)

947-950

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cites work

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

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17318302

retrieved

12 December 2020

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inferred from PubMed ID database lookup

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

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17318302

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12 December 2020

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Frontotemporal dementia and parkinsonism with the P301S tau gene mutation in a Jewish family

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17318302

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12 December 2020

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inferred from PubMed ID database lookup

Differences in a dinucleotide repeat polymorphism in the tau gene between Caucasian and Japanese populations: implication for progressive supranuclear palsy

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17318302

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12 December 2020

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Hereditary tauopathies and parkinsonism

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17318302

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12 December 2020

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

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17318302

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12 December 2020

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

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17318302

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12 December 2020

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

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17318302

retrieved

12 December 2020

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inferred from PubMed ID database lookup

Corticobasal degeneration and progressive supranuclear palsy share a common tau haplotype

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/17318302

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1007/S00702-007-0632-9

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PubMed publication ID

17318302

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