The objective of this study is to report the role of MRI in the diagnosis of sporadic Creutzfeldt-Jakob disease. Materiels and Methods: Two cases report of Creutzfeldt-Jakob\\\'s disease collected at the neuroradiology department with collaboration at the neurology department between 2004-2009 and explored by an encephalic MRI. Results: The age was 53 years for the first case and 70years for the second. The diagnosis of sporadic CJD was retained based on his clinical status including dementia-related deterioration with myoclonus, on brain MRI data showing hyperintensities at the level of the striatum and the cortex on Flair and diffusion-weighted imaging sequences, the results of the electroencephalogram (EEG) and 14-3-3proteins test. Concl...
BACKGROUND Creutzfeldt-Jacob disease ( CJD) is the most common transmissible human spongiform enceph...
Introduction: Creutzfeldt-Jakob disease is manifested by a rapidly progressive dementia, myoclonus a...
Introduction: Creutzfeldt-Jakob disease is manifested by a rapidly progressive dementia, myoclonus a...
Background: Creutzfeldt-Jakob disease (CJD) is a rare progressive neurodegenerative disorder, caused...
ABSTRACT Creutzfeldt-Jacob disease (CJD) is a rare condition caused by a pathogenic prion protein th...
Creutzfeldt-Jakob Disease (CJD) is characterised by subacute progressive dementia, cerebellar ataxi...
Creutzfeldt-Jacob Disease is a prion disease which has a wide range of clinical presentations. Its d...
Creutzfeldt-Jakob disease (CJD) is a rare, degenerative, invariably fatal brain disorder. CJD usuall...
Creutzfeldt-Jakob disease (CJD) is a spongiform encephalopathy with the fatal outcome, caused by the...
Abstract A rapidly progressing dementia, followed by focal neurological signs, and evidence of peri...
Creuzfeldt-Jakobs Disease is a rare neurodegenerative disorder that is included among the transmissi...
imaging in the early diagnosis and monitoring of the pro-gression of a histopathologically proved ca...
© 2016, Sociedad Medica de Santiago. All rights reserved. Creutzfeldt-Jakob disease has a higher inc...
Scientific backround: Clinical picture of sporadic Creutzfeldt-Jakob Disease (s CJD) is composed of ...
Laboratory studies such as electroencephalography, cerebrospinal fluid examination and diffusion-wei...
BACKGROUND Creutzfeldt-Jacob disease ( CJD) is the most common transmissible human spongiform enceph...
Introduction: Creutzfeldt-Jakob disease is manifested by a rapidly progressive dementia, myoclonus a...
Introduction: Creutzfeldt-Jakob disease is manifested by a rapidly progressive dementia, myoclonus a...
Background: Creutzfeldt-Jakob disease (CJD) is a rare progressive neurodegenerative disorder, caused...
ABSTRACT Creutzfeldt-Jacob disease (CJD) is a rare condition caused by a pathogenic prion protein th...
Creutzfeldt-Jakob Disease (CJD) is characterised by subacute progressive dementia, cerebellar ataxi...
Creutzfeldt-Jacob Disease is a prion disease which has a wide range of clinical presentations. Its d...
Creutzfeldt-Jakob disease (CJD) is a rare, degenerative, invariably fatal brain disorder. CJD usuall...
Creutzfeldt-Jakob disease (CJD) is a spongiform encephalopathy with the fatal outcome, caused by the...
Abstract A rapidly progressing dementia, followed by focal neurological signs, and evidence of peri...
Creuzfeldt-Jakobs Disease is a rare neurodegenerative disorder that is included among the transmissi...
imaging in the early diagnosis and monitoring of the pro-gression of a histopathologically proved ca...
© 2016, Sociedad Medica de Santiago. All rights reserved. Creutzfeldt-Jakob disease has a higher inc...
Scientific backround: Clinical picture of sporadic Creutzfeldt-Jakob Disease (s CJD) is composed of ...
Laboratory studies such as electroencephalography, cerebrospinal fluid examination and diffusion-wei...
BACKGROUND Creutzfeldt-Jacob disease ( CJD) is the most common transmissible human spongiform enceph...
Introduction: Creutzfeldt-Jakob disease is manifested by a rapidly progressive dementia, myoclonus a...
Introduction: Creutzfeldt-Jakob disease is manifested by a rapidly progressive dementia, myoclonus a...