Relationships between clinicopathological features and cerebrospinal fluid biomarkers in Japanese patients with genetic prion diseases. (Q34652909)

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27 February 2020

title

Relationships between clinicopathological features and cerebrospinal fluid biomarkers in Japanese patients with genetic prion diseases (English)

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27 February 2020

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27 February 2020

author name string

Maya Higuma

1

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27 February 2020

Katsuya Satoh

3

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27 February 2020

Yusei Shiga

4

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27 February 2020

Kenji Sakai

5

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27 February 2020

Ichiro Nozaki

6

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27 February 2020

Tsuyoshi Hamaguchi

7

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27 February 2020

Yosikazu Nakamura

8

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27 February 2020

Tetsuyuki Kitamoto

9

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27 February 2020

Susumu Shirabe

10

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27 February 2020

Shigeo Murayama

11

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27 February 2020

Masahito Yamada

12

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27 February 2020

Jun Tateishi

13

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27 February 2020

Hidehiro Mizusawa

14

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27 February 2020

language of work or name

English

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publication date

28 March 2013

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27 February 2020

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27 February 2020

volume

8

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issue

3

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27 February 2020

page(s)

e60003

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Creative Commons Attribution 4.0 International

27 February 2020

copyright license

start time

28 March 2013

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April 2022 Public Data File from Crossref

copyright status

copyrighted

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cites work

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Establishment of a standard 14-3-3 protein assay of cerebrospinal fluid as a diagnostic tool for Creutzfeldt-Jakob disease

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Mutations at codons 178, 200-129, and 232 contributed to the inherited prion diseases in Korean patients

7 July 2018

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Phenotypic heterogeneity and genetic modification of P102L inherited prion disease in an international series

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PRNP mutations in a series of apparently sporadic neurodegenerative dementias in China

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Clinical features of Creutzfeldt-Jakob disease with V180I mutation

7 July 2018

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An inherited prion disease with a PrP P105L mutation: clinicopathologic and PrP heterogeneity

7 July 2018

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Creutzfeldt-Jakob disease with florid-type plaques after cadaveric dura mater grafting

7 July 2018

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Different patterns of truncated prion protein fragments correlate with distinct phenotypes in P102L Gerstmann-Sträussler-Scheinker disease

7 July 2018

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Molecular basis of phenotypic variability in sporadic Creutzfeldt-Jakob disease

7 July 2018

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Novel missense variants of prion protein in Creutzfeldt-Jakob disease or Gerstmann-Sträussler syndrome

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Abnormal isoform of prion proteins accumulates in the synaptic structures of the central nervous system in patients with Creutzfeldt-Jakob disease

7 July 2018

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27 February 2020

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