textabstractSeveral molecular subtypes of sporadic Creutzfeldt-Jakob disease have been identified and electroencephalogram and cerebrospinal fluid biomarkers have been reported to support clinical diagnosis but with variable utility according to subtype. In recent years, a series of publications have demonstrated a potentially important role for magnetic resonance imaging in the pre-mortem diagnosis of sporadic Creutzfeldt-Jakob disease. Magnetic resonance imaging signal alterations correlate with distinct sporadic Creutzfeldt-Jakob disease molecular subtypes and thus might contribute to the earlier identification of the whole spectrum of sporadic Creutzfeldt-Jakob disease cases. This multi-centre international study aimed to provide a rati...
Historically various CJD syndromes have been described with a spectrum of clinical presentations. Sp...
Sporadic Creutzfeldt-Jakob disease (CJD), the most common human prion disease, is generally regarded...
Historically various CJD syndromes have been described with a spectrum of clinical presentations. Sp...
Several molecular subtypes of sporadic Creutzfeldt-Jakob disease have been identified and electroenc...
Several molecular subtypes of sporadic Creutzfeldt-Jakob disease have been identified and electroenc...
International audienceBACKGROUND: With respect to sporadic Creutzfeldt-Jakob disease (sCJD), six mol...
Abstract A rapidly progressing dementia, followed by focal neurological signs, and evidence of peri...
BACKGROUND AND PURPOSE: Hyperintense basal ganglia on MR imaging support the diagnosis of sporadic C...
Rapidly progressive dementia (RPD) is a rare presentation of different neurological disorders charac...
Introduction: Sporadic Creutzfeldt-Jakob disease (sCJD) comprises multiple subtypes (MM1, MM2, MV1, ...
Rapidly progressive dementia (RPD) is a rare presentation of different neurological disorders charac...
Background: Creutzfeldt-Jakob disease (CJD) is a rare progressive neurodegenerative disorder, caused...
The definitive diagnosis of sporadic Creutzfeldt-Jakob disease (sCJD) is based on brain autopsy. The...
A 75-year-old woman with unremarkable medical history, consulted for a 5-month history of involuntar...
Creutzfeldt-Jakob disease (CJD) is a spongiform encephalopathy with the fatal outcome, caused by the...
Historically various CJD syndromes have been described with a spectrum of clinical presentations. Sp...
Sporadic Creutzfeldt-Jakob disease (CJD), the most common human prion disease, is generally regarded...
Historically various CJD syndromes have been described with a spectrum of clinical presentations. Sp...
Several molecular subtypes of sporadic Creutzfeldt-Jakob disease have been identified and electroenc...
Several molecular subtypes of sporadic Creutzfeldt-Jakob disease have been identified and electroenc...
International audienceBACKGROUND: With respect to sporadic Creutzfeldt-Jakob disease (sCJD), six mol...
Abstract A rapidly progressing dementia, followed by focal neurological signs, and evidence of peri...
BACKGROUND AND PURPOSE: Hyperintense basal ganglia on MR imaging support the diagnosis of sporadic C...
Rapidly progressive dementia (RPD) is a rare presentation of different neurological disorders charac...
Introduction: Sporadic Creutzfeldt-Jakob disease (sCJD) comprises multiple subtypes (MM1, MM2, MV1, ...
Rapidly progressive dementia (RPD) is a rare presentation of different neurological disorders charac...
Background: Creutzfeldt-Jakob disease (CJD) is a rare progressive neurodegenerative disorder, caused...
The definitive diagnosis of sporadic Creutzfeldt-Jakob disease (sCJD) is based on brain autopsy. The...
A 75-year-old woman with unremarkable medical history, consulted for a 5-month history of involuntar...
Creutzfeldt-Jakob disease (CJD) is a spongiform encephalopathy with the fatal outcome, caused by the...
Historically various CJD syndromes have been described with a spectrum of clinical presentations. Sp...
Sporadic Creutzfeldt-Jakob disease (CJD), the most common human prion disease, is generally regarded...
Historically various CJD syndromes have been described with a spectrum of clinical presentations. Sp...