(Q46927023)

26 December 2017

title

Two different clinical phenotypes of Creutzfeldt-Jakob disease with a M232R substitution (English)

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26 December 2017

Creutzfeldt-Jakob disease

main subject

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5

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26 December 2017

author name string

Yusei Shiga

1

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26 December 2017

Katsuya Satoh

2

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26 December 2017

Tetsuyuki Kitamoto

3

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26 December 2017

Sigenori Kanno

4

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26 December 2017

Shigeru Sato

6

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26 December 2017

Kazuo Fujihara

7

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26 December 2017

Hiroshi Takata

8

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26 December 2017

Keigo Nobukuni

9

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26 December 2017

Shigetoshi Kuroda

10

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26 December 2017

Hiroki Takano

11

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26 December 2017

Yoshitaka Umeda

12

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26 December 2017

Hidehiko Konno

13

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26 December 2017

Kunihiko Nagasato

14

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26 December 2017

Akira Satoh

15

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26 December 2017

Yoshito Matsuda

16

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26 December 2017

Mitsuru Hidaka

17

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26 December 2017

Hirokatsu Takahashi

18

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26 December 2017

Yasuteru Sano

19

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26 December 2017

Kang Kim

20

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26 December 2017

Takashi Konishi

21

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26 December 2017

Katsumi Doh-ura

22

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26 December 2017

Takeshi Sato

23

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26 December 2017

Kensuke Sasaki

24

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26 December 2017

Yoshikazu Nakamura

25

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26 December 2017

Masahito Yamada

26

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26 December 2017

Hidehiro Mizusawa

27

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26 December 2017

Yasuo Itoyama

28

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26 December 2017

publication date

2 November 2007

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26 December 2017

published in

Journal of Neurology

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26 December 2017

volume

254

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26 December 2017

issue

11

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26 December 2017

page(s)

1509-1517

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26 December 2017

https://scigraph.springernature.com/pub.10.1007/s00415-007-0540-9

exact match

0 references

cites work

Diffusion-weighted MRI abnormalities as an early diagnostic marker for Creutzfeldt-Jakob disease

1 reference

https://api.crossref.org/works/10.1007%2FS00415-007-0540-9

A patient with dementia with Lewy bodies and codon 232 mutation of PRNP.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-007-0540-9

Clinical features of Creutzfeldt-Jakob disease with V180I mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-007-0540-9

Fatal insomnia in a case of familial Creutzfeldt-Jakob disease with the codon 200(Lys) mutation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-007-0540-9

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-007-0540-9

Insomnia associated with thalamic involvement in E200K Creutzfeldt-Jakob disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-007-0540-9

Clinical diagnosis of MM2-type sporadic Creutzfeldt-Jakob disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-007-0540-9

Humanized knock-in mice expressing chimeric prion protein showed varied susceptibility to different human prions

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00415-007-0540-9

Genetic prion disease: the EUROCJD experience.

21 January 2018

1 reference

12 December 2020

Spontaneous mutations in the prion protein gene causing transmissible spongiform encephalopathy

1 reference

12 December 2020

Codon 219 Lys allele of PRNP is not found in sporadic Creutzfeldt-Jakob disease

1 reference

12 December 2020

A case of Creutzfeldt-Jakob disease with a point mutation at codon 232: correlation of MRI and neurologic findings

1 reference

12 December 2020

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

1 reference

12 December 2020

Mutation in the prion protein gene at codon 232 in Japanese patients with Creutzfeldt-Jakob disease: a clinicopathological, immunohistochemical and transmission study.

1 reference

12 December 2020

Predictors of survival in sporadic Creutzfeldt-Jakob disease and other human transmissible spongiform encephalopathies.

1 reference

12 December 2020

Association of an 11-12 kDa protease-resistant prion protein fragment with subtypes of dura graft-associated Creutzfeldt-Jakob disease and other prion diseases

1 reference

12 December 2020

A novel phenotype in familial Creutzfeldt-Jakob disease: prion protein gene E200K mutation coupled with valine at codon 129 and type 2 protease-resistant prion protein.

1 reference

12 December 2020

Mutations of the prion protein gene phenotypic spectrum

1 reference

12 December 2020

Double mutations at codon 180 and codon 232 of the PRNP gene in an apparently sporadic case of Creutzfeldt-Jakob disease

1 reference

12 December 2020

Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects

1 reference

12 December 2020

Gerstmann-Sträussler-Scheinker disease with the PRNP P102L mutation and valine at codon 129

1 reference

12 December 2020

Polymorphism at codon 129 or codon 219 of PRNP and clinical heterogeneity in a previously unreported family with Gerstmann-Sträussler-Scheinker disease (PrP-P102L mutation)

1 reference

12 December 2020

Fatal familial insomnia and familial Creutzfeldt-Jakob disease: disease phenotype determined by a DNA polymorphism

1 reference

12 December 2020

Creutzfeldt-Jakob disease with E200K mutation in Slovakia: characterization and development.

1 reference

12 December 2020

Pro----leu change at position 102 of prion protein is the most common but not the sole mutation related to Gerstmann-Sträussler syndrome

1 reference

12 December 2020

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

1 reference

12 December 2020

Fatal familial insomnia and familial Creutzfeldt-Jakob disease: different prion proteins determined by a DNA polymorphism

1 reference

12 December 2020

Molecular classification of sporadic Creutzfeldt-Jakob disease.

1 reference

12 December 2020

New variant prion protein in a Japanese family with Gerstmann-Sträussler syndrome

1 reference

12 December 2020

Diffusion-weighted and fluid-attenuated inversion recovery imaging in Creutzfeldt-Jakob disease: high sensitivity and specificity for diagnosis.

1 reference

12 December 2020

10.1007/S00415-007-0540-9

Identifiers

DOI

1 reference

26 December 2017

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26 December 2017