The current classification of human sporadic prion diseases recognizes six major phenotypic subtypes with distinctive clinicopathological features, which largely correlate at the molecular level with the genotype at the polymorphic codon 129 (methionine, M, or valine, V) in the prion protein gene and with the size of the proteaseresistant core of the abnormal prion protein, PrP Sc (i.e. type 1 migrating at 21 kDa and type 2 at 19 kDa). We previously demonstrated that PrPSc typing by Western blotting is a reliable means of strain typing and disease classification. Limitations of this approach, however, particularly in the interlaboratory setting, are the association of PrPSc types 1 or 2 with more than one clinicopathological phenotype, whic...
Six subtypes of sporadic Creutzfeldt–Jakob disease with distinctive clinico-pathological features ha...
The purpose of this study was to perform an updated reclassification of all definite prion disease c...
Sporadic Creutzfeldt-Jakob disease (sCJD) is the most common form of CJD and is believed to be cause...
The current classification of human sporadic prion diseases recognizes six major phenotypic subtypes...
none18siThe current classification of human sporadic prion diseases recognizes six major phenotypic ...
none2noHuman prion diseases are a unique group of transmissible neurodegenerative diseases that occu...
Human prion diseases are rare neurodegenerative disorders related to prion protein misfolding that c...
Molecular typing in Creutzfeld-Jakob disease (CJD) is of considerable importance for the surveillanc...
BACKGROUND: Prion diseases are a group of invariably fatal neurodegenerative disorders affecting hum...
While rare in humans, the prion diseases have become an area of intense clinical and scientific inte...
Six subtypes of sporadic Creutzfeldt-Jakob disease with distinctive clinico-pathological features ha...
Sporadic Creutzfeldt-Jakob disease (sCJD) cases are currently subclassified according to the methion...
Sporadic Creutzfeldt-Jakob disease (sCJD) cases are currently subclassified according to the methion...
According to the protein-only hypothesis of prion propagation, an abnormal isoform (designated PrPSc...
<div><h3>Background</h3><p>Prion diseases are a group of invariably fatal neurodegenerative disorder...
Six subtypes of sporadic Creutzfeldt–Jakob disease with distinctive clinico-pathological features ha...
The purpose of this study was to perform an updated reclassification of all definite prion disease c...
Sporadic Creutzfeldt-Jakob disease (sCJD) is the most common form of CJD and is believed to be cause...
The current classification of human sporadic prion diseases recognizes six major phenotypic subtypes...
none18siThe current classification of human sporadic prion diseases recognizes six major phenotypic ...
none2noHuman prion diseases are a unique group of transmissible neurodegenerative diseases that occu...
Human prion diseases are rare neurodegenerative disorders related to prion protein misfolding that c...
Molecular typing in Creutzfeld-Jakob disease (CJD) is of considerable importance for the surveillanc...
BACKGROUND: Prion diseases are a group of invariably fatal neurodegenerative disorders affecting hum...
While rare in humans, the prion diseases have become an area of intense clinical and scientific inte...
Six subtypes of sporadic Creutzfeldt-Jakob disease with distinctive clinico-pathological features ha...
Sporadic Creutzfeldt-Jakob disease (sCJD) cases are currently subclassified according to the methion...
Sporadic Creutzfeldt-Jakob disease (sCJD) cases are currently subclassified according to the methion...
According to the protein-only hypothesis of prion propagation, an abnormal isoform (designated PrPSc...
<div><h3>Background</h3><p>Prion diseases are a group of invariably fatal neurodegenerative disorder...
Six subtypes of sporadic Creutzfeldt–Jakob disease with distinctive clinico-pathological features ha...
The purpose of this study was to perform an updated reclassification of all definite prion disease c...
Sporadic Creutzfeldt-Jakob disease (sCJD) is the most common form of CJD and is believed to be cause...