Prion infectivity in the spleen of a PRNP heterozygous individual with subclinical variant Creutzfeldt–Jakob diseas
phalopathiesare neurodegenerative diseasescaused by abnormal accumulation of pathogenicisoform the p...
Prion diseases are a group of diseases caused by abnormally conformed infectious proteins, called pr...
BACKGROUND: Prion diseases are a group of invariably fatal neurodegenerative disorders affecting hum...
Prion infectivity in the spleen of a PRNP heterozygous individual with subclinical variant Creutzfel...
Agent strain variation in human prion disease: insights from a molecular and pathologica
subtypes or a spectrum of disease? Although the condition we now call sporadic Creutzfeldt–Jakob dis...
<div><h3>Background</h3><p>Prion diseases are a group of invariably fatal neurodegenerative disorder...
Human prion diseases can occur as an idiopathic disorder (sporadic Creutzfeldt–Jakob disease) or can...
Human prion diseases are fatal neurodegenerative disorders associated with an accumulation of PrPSc ...
Application of an immunocapillary electrophoresis assay to the detection of abnormal prion protein i...
Abstract Prion diseases are neurodegenerative disorders which are caused by an accumulation of the a...
A characteristic feature of Creutzfeldt-jakob disease (CJD) is the accumulation in the brain of the ...
Fulltext embargoed for: 12 months post date of publicationSporadic Creutzfeldt-Jakob disease (CJD) i...
none4noPrion diseases are progressive neurodegenerative disorders affecting humans and other mammali...
Eva Bagyinszky,1 Vo Van Giau,1 Young Chul Youn,2 Seong Soo A An,1 SangYun Kim3 1Department of Biona...
phalopathiesare neurodegenerative diseasescaused by abnormal accumulation of pathogenicisoform the p...
Prion diseases are a group of diseases caused by abnormally conformed infectious proteins, called pr...
BACKGROUND: Prion diseases are a group of invariably fatal neurodegenerative disorders affecting hum...
Prion infectivity in the spleen of a PRNP heterozygous individual with subclinical variant Creutzfel...
Agent strain variation in human prion disease: insights from a molecular and pathologica
subtypes or a spectrum of disease? Although the condition we now call sporadic Creutzfeldt–Jakob dis...
<div><h3>Background</h3><p>Prion diseases are a group of invariably fatal neurodegenerative disorder...
Human prion diseases can occur as an idiopathic disorder (sporadic Creutzfeldt–Jakob disease) or can...
Human prion diseases are fatal neurodegenerative disorders associated with an accumulation of PrPSc ...
Application of an immunocapillary electrophoresis assay to the detection of abnormal prion protein i...
Abstract Prion diseases are neurodegenerative disorders which are caused by an accumulation of the a...
A characteristic feature of Creutzfeldt-jakob disease (CJD) is the accumulation in the brain of the ...
Fulltext embargoed for: 12 months post date of publicationSporadic Creutzfeldt-Jakob disease (CJD) i...
none4noPrion diseases are progressive neurodegenerative disorders affecting humans and other mammali...
Eva Bagyinszky,1 Vo Van Giau,1 Young Chul Youn,2 Seong Soo A An,1 SangYun Kim3 1Department of Biona...
phalopathiesare neurodegenerative diseasescaused by abnormal accumulation of pathogenicisoform the p...
Prion diseases are a group of diseases caused by abnormally conformed infectious proteins, called pr...
BACKGROUND: Prion diseases are a group of invariably fatal neurodegenerative disorders affecting hum...