Creutzfeldt-Jakob disease segregating in a three generation Danish family (Q32153658)

6 July 2017

title

Creutzfeldt-Jakob disease segregating in a three generation Danish family (English)

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Creutzfeldt-Jakob disease

6 July 2017

main subject

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Holm IE

1

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6 July 2017

Abelskov K

2

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6 July 2017

Bojsen-Møller M

3

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6 July 2017

Nielsen AL

4

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6 July 2017

Jørgensen AL

5

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6 July 2017

language of work or name

English

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publication date

1 March 2001

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Acta Neurologica Scandinavica

6 July 2017

published in

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6 July 2017

volume

103

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6 July 2017

issue

3

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6 July 2017

page(s)

139-147

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Human spongiform encephalopathy: the National Institutes of Health series of 300 cases of experimentally transmitted disease

6 July 2017

cites work

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

21 January 2018

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Creutzfeldt-Jakob disease: Patterns of worldwide occurrence and the significance of familial and sporadic clustering

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Assignment of the human and mouse prion protein genes to homologous chromosomes

21 January 2018

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Molecular cloning of a human prion protein cDNA

21 January 2018

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Complete genomic sequence and analysis of the prion protein gene region from three mammalian species

21 January 2018

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Genetic basis of Creutzfeldt-Jakob disease in the United Kingdom: a systematic analysis of predisposing mutations and allelic variation in the PRNP gene

21 January 2018

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21 January 2018

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Molecular genetics of human prion diseases in Germany

21 January 2018

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Genetic predisposition to iatrogenic Creutzfeldt-Jakob disease

21 January 2018

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

21 January 2018

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Homozygous prion protein genotype predisposes to sporadic Creutzfeldt–Jakob disease

21 January 2018

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Fatal familial insomnia and familial Creutzfeldt-Jakob disease: clinical, pathological and molecular features.

21 January 2018

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A PrP gene codon 178 base substitution and a 24-bp interstitial deletion in familial Creutzfeldt-Jakob disease

21 January 2018

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

21 January 2018

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Tau is a candidate gene for chromosome 17 frontotemporal dementia

21 January 2018

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Structure and novel exons of the human tau gene

21 January 2018

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APOE in non-Alzheimer amyloidoses: transmissible spongiform encephalopathies

21 January 2018

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

21 January 2018

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

21 January 2018

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7 January 2021

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

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7 January 2021

Codon 178 mutation of the human prion protein gene in a German family (Backer family): sequencing data from 72-year-old celloidin-embedded brain tissue

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7 January 2021

Identification in Israel of 2 Jewish Creutzfeld-Jakob disease patients with a 178 mutation at their PrP gene

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7 January 2021

Sequence variation in intron of prion protein gene, crucial for complete diagnostic strategies

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7 January 2021

New mutation in scrapie amyloid precursor gene (at codon 178) in Finnish Creutzfeldt-Jakob kindred

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7 January 2021

10.1034/J.1600-0404.2001.103003139.X

Identifiers

DOI

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6 July 2017

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