Panencephalitic Creutzfeldt-Jakob disease in a Chinese family. Unusual presentation with PrP codon 210 mutation and identification by PCR-SSCP. (Q48869592)

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English	Panencephalitic Creutzfeldt-Jakob disease in a Chinese family. Unusual presentation with PrP codon 210 mutation and identification by PCR-SSCP.	scientific article

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scholarly article

1 reference

Europe PubMed Central

16 February 2018

http://europepmc.org/abstract/MED/8981320

Panencephalitic Creutzfeldt-Jakob disease in a Chinese family. Unusual presentation with PrP codon 210 mutation and identification by PCR-SSCP. (English)

1 reference

Europe PubMed Central

16 February 2018

http://europepmc.org/abstract/MED/8981320

Creutzfeldt-Jakob disease

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based on heuristic

inferred from title

author name string

Shyu WC

1

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Europe PubMed Central

16 February 2018

http://europepmc.org/abstract/MED/8981320

Hsu YD

2

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Europe PubMed Central

16 February 2018

http://europepmc.org/abstract/MED/8981320

Kao MC

3

1 reference

Europe PubMed Central

16 February 2018

http://europepmc.org/abstract/MED/8981320

Tsao WL

4

1 reference

Europe PubMed Central

16 February 2018

http://europepmc.org/abstract/MED/8981320

publication date

1 November 1996

1 reference

Europe PubMed Central

16 February 2018

http://europepmc.org/abstract/MED/8981320

number of pages

5

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inferred from page(s)

Journal of the Neurological Sciences

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Europe PubMed Central

16 February 2018

http://europepmc.org/abstract/MED/8981320

143

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Europe PubMed Central

16 February 2018

http://europepmc.org/abstract/MED/8981320

1-2

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16 February 2018

http://europepmc.org/abstract/MED/8981320

176-180

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Europe PubMed Central

16 February 2018

http://europepmc.org/abstract/MED/8981320

Creutzfeldt-Jakob disease prion proteins in human brains

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2896%2900198-0

7 January 2021

Creutzfeldt-Jakob disease of long duration: clinicopathological characteristics, transmissibility, and differential diagnosis.

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2896%2900198-0

7 January 2021

Creutzfeldt-Jakob disease: clinical analysis of a consecutive series of 230 neuropathologically verified cases.

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2896%2900198-0

7 January 2021

Familial Creutzfeldt-Jakob disease in Chile is associated with the codon 200 mutation of the PRNP amyloid precursor gene on chromosome 20.

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2896%2900198-0

7 January 2021

Phenotypic characteristics of familial Creutzfeldt-Jakob disease associated with the codon 178Asn PRNP mutation

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2896%2900198-0

7 January 2021

Transmissible familial Creutzfeldt-Jakob disease associated with five, seven, and eight extra octapeptide coding repeats in the PRNP gene

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2896%2900198-0

7 January 2021

Creutzfeldt-Jakob disease cosegregates with the codon 178Asn PRNP mutation in families of European origin

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2896%2900198-0

7 January 2021

Japanese family with Creutzfeldt-Jakob disease with codon 200 point mutation of the prion protein gene.

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2896%2900198-0

7 January 2021

Molecular cloning of a human prion protein cDNA

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https://api.crossref.org/works/10.1016%2FS0022-510X%2896%2900198-0

7 January 2021

Panencephalopathic type of Creutzfeldt-Jakob disease: primary involvement of the cerebral white matter

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2896%2900198-0

7 January 2021

Rapid and sensitive detection of point mutations and DNA polymorphisms using the polymerase chain reaction

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2896%2900198-0

7 January 2021

A new point mutation of the prion protein gene in Creutzfeldt-Jakob disease.

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2896%2900198-0

7 January 2021

A new point mutation in the prion protein gene at codon 210 in Creutzfeldt-Jakob disease

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2896%2900198-0

7 January 2021

Creutzfeldt-Jakob disease. Report of a case of the panencephalopathic type and experiences of a teaching hospital in Taiwan.

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2896%2900198-0

7 January 2021

Serial MR imaging in Creutzfeldt-Jakob disease

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2896%2900198-0

7 January 2021

The 717Val----Ile substitution in amyloid precursor protein is associated with familial Alzheimer's disease regardless of ethnic groups.

1 reference

https://api.crossref.org/works/10.1016%2FS0022-510X%2896%2900198-0

7 January 2021

Identifiers

10.1016/S0022-510X(96)00198-0

1 reference

Europe PubMed Central

16 February 2018

http://europepmc.org/abstract/MED/8981320

1 reference

Europe PubMed Central

16 February 2018

http://europepmc.org/abstract/MED/8981320

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