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

Detection of prion seeding activity in the olfactory mucosa of patients with Fatal Familial Insomnia.

Creutzfeldt-Jakob Disease with a prion protein gene codon 180 mutation presenting asymmetric cortical high-intensity on magnetic resonance imaging.

Prion disease: A newly identified mutation in prion protein is associated with diarrhoea and autonomic neuropathy.

Codon 129 changes in the prion protein gene in Caucasians.

Creutzfeldt-Jakob disease associated with a V203I homozygous mutation in the prion protein gene.

Transgenic fatal familial insomnia mice indicate prion infectivity-independent mechanisms of pathogenesis and phenotypic expression of disease.

Association of prion protein genotype and scrapie prion protein type with cellular prion protein charge isoform profiles in cerebrospinal fluid of humans with sporadic or familial prion diseases.

Correction: Transgenic Fatal Familial Insomnia Mice Indicate Prion Infectivity-Independent Mechanisms of Pathogenesis and Phenotypic Expression of Disease.

Clinical features of genetic Creutzfeldt-Jakob disease with V180I mutation in the prion protein gene.

A naturally occurring variant of the human prion protein completely prevents prion disease.

Uncommon phenotype for a codon 178 mutation of the human PrP gene.

Alzheimer's disease and prion protein.

Deletion in the prion protein gene in a demented patient.

Treatment of Prion Disease with Heterologous Prion Proteins.

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

Prion protein scrapie and the normal cellular prion protein.

Mutation of the prion protein in Libyan Jews with Creutzfeldt-Jakob disease.

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

Serial magnetic resonance imaging changes in sporadic Creutzfeldt-Jakob disease with valine homozygosity at codon 129 of the prion protein gene.

Correction: Fatal Prion Disease in a Mouse Model of Genetic E200K Creutzfeldt-Jakob Disease.

What makes a protein sequence a prion?

Prion disease.

V and type 2 abnormal prion protein.

Disease Transmission by Misfolded Prion-Protein Isoforms, Prion-Like Amyloids, Functional Amyloids and the Central Dogma.

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Detection of prion seeding activity in the olfactory mucosa of patients with Fatal Familial Insomnia.

Creutzfeldt-Jakob Disease with a prion protein gene codon 180 mutation presenting asymmetric cortical high-intensity on magnetic resonance imaging.

Prion disease: A newly identified mutation in prion protein is associated with diarrhoea and autonomic neuropathy.

Codon 129 changes in the prion protein gene in Caucasians.

Creutzfeldt-Jakob disease associated with a V203I homozygous mutation in the prion protein gene.

Transgenic fatal familial insomnia mice indicate prion infectivity-independent mechanisms of pathogenesis and phenotypic expression of disease.

Association of prion protein genotype and scrapie prion protein type with cellular prion protein charge isoform profiles in cerebrospinal fluid of humans with sporadic or familial prion diseases.

Correction: Transgenic Fatal Familial Insomnia Mice Indicate Prion Infectivity-Independent Mechanisms of Pathogenesis and Phenotypic Expression of Disease.

Clinical features of genetic Creutzfeldt-Jakob disease with V180I mutation in the prion protein gene.

A naturally occurring variant of the human prion protein completely prevents prion disease.

Uncommon phenotype for a codon 178 mutation of the human PrP gene.

Alzheimer's disease and prion protein.

Deletion in the prion protein gene in a demented patient.

Treatment of Prion Disease with Heterologous Prion Proteins.

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

Prion protein scrapie and the normal cellular prion protein.

Mutation of the prion protein in Libyan Jews with Creutzfeldt-Jakob disease.

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

Serial magnetic resonance imaging changes in sporadic Creutzfeldt-Jakob disease with valine homozygosity at codon 129 of the prion protein gene.

Correction: Fatal Prion Disease in a Mouse Model of Genetic E200K Creutzfeldt-Jakob Disease.

What makes a protein sequence a prion?

Prion disease.

V and type 2 abnormal prion protein.

Disease Transmission by Misfolded Prion-Protein Isoforms, Prion-Like Amyloids, Functional Amyloids and the Central Dogma.

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

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