The prion diseases: Creutzfeldt-Jakob, Gerstmann-Sträussler-Scheinker, and related disorders. (Q48313878)

10 February 2018

review article

1 reference

title

The prion diseases: Creutzfeldt-Jakob, Gerstmann-Sträussler-Scheinker, and related disorders. (English)

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10 February 2018

0 references

J A Mastrianni

1

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10 February 2018

publication date

1 January 1998

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10 February 2018

Journal of Geriatric Psychiatry and Neurology

published in

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10 February 2018

volume

11

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10 February 2018

issue

2

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10 February 2018

page(s)

78-97

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10 February 2018

Experimental transmission of a Kuru-like syndrome to chimpanzees

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Degeneration of skeletal muscle, peripheral nerves, and the central nervous system in transgenic mice overexpressing wild-type prion proteins

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Prion protein is necessary for normal synaptic function.

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PrP gene dosage and long term potentiation

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The cellular prion protein binds copper in vivo

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Prion protein selectively binds copper(II) ions

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Mice deficient for prion protein exhibit normal neuronal excitability and synaptic transmission in the hippocampus

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Linkage of a prion protein missense variant to Gerstmann-Sträussler syndrome

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Neurofibrillary tangles of the Indiana kindred of Gerstmann-Sträussler-Scheinker disease share antigenic determinants with those of Alzheimer disease.

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Vascular variant of prion protein cerebral amyloidosis with tau-positive neurofibrillary tangles: the phenotype of the stop codon 145 mutation in PRNP.

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Selective neuronal targeting in prion disease

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

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

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The Ataxic Form of Creutzfeldt-Jakob Disease

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Transmission of Creutzfeldt-Jakob disease from humans to transgenic mice expressing chimeric human-mouse prion protein

21 January 2018

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Iatrogenic Creutzfeldt-Jakob disease in three growth hormone recipients: a neuropathological study.

21 January 2018

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Potential epidemic of Creutzfeldt-Jakob disease from human growth hormone therapy.

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Creutzfeldt-Jakob disease infectivity of growth hormone derived from human pituitary glands.

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Creutzfeldt-Jacob disease following cadaveric dura mater graft

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Creutzfeldt-Jakob disease in a patient with a cadaveric dural graft.

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Letter: Hepatitis with hindsight

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Creutzfeldt-Jakob disease in a recipient of human pituitary-derived gonadotrophin: a second case

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Prion protein amyloidosis

21 January 2018

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Fatal familial insomnia, a prion disease with a mutation at codon 178 of the prion protein gene

21 January 2018

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Fatal familial insomnia: a second kindred with mutation of prion protein gene at codon 178

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Analysis of the prion protein gene in thalamic dementia

21 January 2018

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21 January 2018

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21 January 2018

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Homozygous prion protein genotype predisposes to sporadic Creutzfeldt–Jakob disease

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Deletions in the prion protein gene are not associated with CJD.

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21 January 2018

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A missense mutation at codon 105 with codon 129 polymorphism of the prion protein gene in a new variant of Gerstmann-Sträussler-Scheinker disease

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A prion protein variant in a family with the telencephalic form of Gerstmann-Straussler-Scheinker syndrome

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21 January 2018

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Chemoprophylaxis of scrapie in mice

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21 January 2018

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https://api.crossref.org/works/10.1177%2F089198879801100206

Atypical Creutzfeldt-Jakob disease in an American family with an insert mutation in the PRNP amyloid precursor gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F089198879801100206

An insert mutation in the chromosome 20 amyloid precursor gene in a Gerstmann-Sträussler-Scheinker family

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F089198879801100206

A dementing illness associated with a novel insertion in the prion protein gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F089198879801100206

Prion disease associated with a novel nine octapeptide repeat insertion in the PRNP gene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F089198879801100206

Altered circadian activity rhythms and sleep in mice devoid of prion protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F089198879801100206

BSE transmission to macaques

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F089198879801100206

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F089198879801100206

10.1177/089198879801100206

21 January 2018

Identifiers

DOI

1 reference

10 February 2018

PubMed ID

9877529

1 reference

10 February 2018