BACKGROUND AND PURPOSE: Hyperintense basal ganglia on MR imaging support the diagnosis of sporadic Creutzfeldt-Jakob disease (CJD). Our aim was to study the frequency of patients with sporadic CJD presenting with and without characteristic basal ganglia lesions on MR imaging and to examine the corresponding patient characteristics. MATERIALS AND METHODS: Fluid-attenuated inversion recovery (FLAIR) and diffusion-weighted im-ages (DWI) of 55 patients with CJD were assessed for signal-intensity increase (FLAIR) or restricted diffusion (DWI) in 7 cortex regions and the basal ganglia, thalamus, and cerebellum. Patient charac-teristics as well as electroencephalography, CSF, and codon 129 genotype of the prion protein gene (PRNP) were correlated ...
BACKGROUND AND PURPOSE: A panencephalopathic type of Creutzfeldt-Jakob disease (pCJD) is characteriz...
Several molecular subtypes of sporadic Creutzfeldt-Jakob disease have been identified and electroenc...
Introduction: Sporadic Creutzfeldt-Jakob disease (sCJD) comprises multiple subtypes (MM1, MM2, MV1, ...
BACKGROUND AND PURPOSE: High cortical signal intensity on diffusion-weighted (DW) or fluid-atten-uat...
International audienceBACKGROUND: With respect to sporadic Creutzfeldt-Jakob disease (sCJD), six mol...
ABSTRACTThe most common genetic Creutzfeldt-Jakob disease (gCJD) in Japan is caused by a point mutat...
imaging in the early diagnosis and monitoring of the pro-gression of a histopathologically proved ca...
Several molecular subtypes of sporadic Creutzfeldt-Jakob disease have been identified and electroenc...
Scientific backround: Clinical picture of sporadic Creutzfeldt-Jakob Disease (s CJD) is composed of ...
Sporadic Creutzfeldt-Jakob disease (CJD), the most common human prion disease, is generally regarded...
Background and purposeSporadic Creutzfeldt-Jakob disease (sCJD) is a rapidly progressive neurodegene...
BACKGROUND AND PURPOSE: MR imaging has played an increasingly important role in the diagnosis of Cre...
BACKGROUND AND PURPOSE: The E200K mutation of the PRNP (prion protein) gene is the most common cause...
ment in sporadic Creutzfeldt-Jakob disease (sCJD), which has been disregarded in imaging studies. Di...
Abstract A rapidly progressing dementia, followed by focal neurological signs, and evidence of peri...
BACKGROUND AND PURPOSE: A panencephalopathic type of Creutzfeldt-Jakob disease (pCJD) is characteriz...
Several molecular subtypes of sporadic Creutzfeldt-Jakob disease have been identified and electroenc...
Introduction: Sporadic Creutzfeldt-Jakob disease (sCJD) comprises multiple subtypes (MM1, MM2, MV1, ...
BACKGROUND AND PURPOSE: High cortical signal intensity on diffusion-weighted (DW) or fluid-atten-uat...
International audienceBACKGROUND: With respect to sporadic Creutzfeldt-Jakob disease (sCJD), six mol...
ABSTRACTThe most common genetic Creutzfeldt-Jakob disease (gCJD) in Japan is caused by a point mutat...
imaging in the early diagnosis and monitoring of the pro-gression of a histopathologically proved ca...
Several molecular subtypes of sporadic Creutzfeldt-Jakob disease have been identified and electroenc...
Scientific backround: Clinical picture of sporadic Creutzfeldt-Jakob Disease (s CJD) is composed of ...
Sporadic Creutzfeldt-Jakob disease (CJD), the most common human prion disease, is generally regarded...
Background and purposeSporadic Creutzfeldt-Jakob disease (sCJD) is a rapidly progressive neurodegene...
BACKGROUND AND PURPOSE: MR imaging has played an increasingly important role in the diagnosis of Cre...
BACKGROUND AND PURPOSE: The E200K mutation of the PRNP (prion protein) gene is the most common cause...
ment in sporadic Creutzfeldt-Jakob disease (sCJD), which has been disregarded in imaging studies. Di...
Abstract A rapidly progressing dementia, followed by focal neurological signs, and evidence of peri...
BACKGROUND AND PURPOSE: A panencephalopathic type of Creutzfeldt-Jakob disease (pCJD) is characteriz...
Several molecular subtypes of sporadic Creutzfeldt-Jakob disease have been identified and electroenc...
Introduction: Sporadic Creutzfeldt-Jakob disease (sCJD) comprises multiple subtypes (MM1, MM2, MV1, ...