Agent strain variation in human prion disease: insights from a molecular and pathologica
Prion diseases which are serious neurodegenerative diseases that affect humans and animals occur in ...
4noIncreasing evidence suggests that neurodegenerative disorders share a common pathogenic feature: ...
AbstractPrions are unconventional infectious agents responsible for transmissible spongiform encepha...
none2noHuman prion diseases are a unique group of transmissible neurodegenerative diseases that occu...
Prions are infectious pathogens principally composed of abnormal forms of a protein encoded in the h...
Prion diseases are a unique group of rare neurodegenerative disorders characterized by tissue deposi...
Prion diseases are a unique group of rare neurodegenerative disorders characterized by tissue deposi...
While rare in humans, the prion diseases have become an area of intense clinical and scientific inte...
none4noPrion diseases are progressive neurodegenerative disorders affecting humans and other mammali...
The infectious agents, prions, are composed mainly of conformational isomers of the cellular prion p...
Increasing evidence suggests that neurodegenerative disorders share a common pathogenic feature: the...
Human prion brain disease has been studied intensely since 1920. Examples of such diseases include C...
Prions are unconventional infectious agents responsible for transmissible spongiform encephalopathie...
Prion diseases are fatal neurodegenerative conditions in humans and animals. In this review, we summ...
Human prion diseases are rare neurodegenerative disorders related to prion protein misfolding that c...
Prion diseases which are serious neurodegenerative diseases that affect humans and animals occur in ...
4noIncreasing evidence suggests that neurodegenerative disorders share a common pathogenic feature: ...
AbstractPrions are unconventional infectious agents responsible for transmissible spongiform encepha...
none2noHuman prion diseases are a unique group of transmissible neurodegenerative diseases that occu...
Prions are infectious pathogens principally composed of abnormal forms of a protein encoded in the h...
Prion diseases are a unique group of rare neurodegenerative disorders characterized by tissue deposi...
Prion diseases are a unique group of rare neurodegenerative disorders characterized by tissue deposi...
While rare in humans, the prion diseases have become an area of intense clinical and scientific inte...
none4noPrion diseases are progressive neurodegenerative disorders affecting humans and other mammali...
The infectious agents, prions, are composed mainly of conformational isomers of the cellular prion p...
Increasing evidence suggests that neurodegenerative disorders share a common pathogenic feature: the...
Human prion brain disease has been studied intensely since 1920. Examples of such diseases include C...
Prions are unconventional infectious agents responsible for transmissible spongiform encephalopathie...
Prion diseases are fatal neurodegenerative conditions in humans and animals. In this review, we summ...
Human prion diseases are rare neurodegenerative disorders related to prion protein misfolding that c...
Prion diseases which are serious neurodegenerative diseases that affect humans and animals occur in ...
4noIncreasing evidence suggests that neurodegenerative disorders share a common pathogenic feature: ...
AbstractPrions are unconventional infectious agents responsible for transmissible spongiform encepha...