he objective of this work is to describe the neuropathological findings of a patient clinically presenting with rapidly progressive nonspecific neurological symptoms suggestive of Creutzfeldt-Jakob disease. Methods used were clinical description with laboratory analyses, repeated electroencephalogram, cerebral computed tomography, magnetic resonance imaging studies and details on neuropathological work-up. Neuropathological examination excluded Creutzfeldt-Jakob disease. By contrast other neurodegenerative changes combining Alzheimer-type pathology and Lewy body pathology were detected as the most likely substrate of neurological symptoms. Dementia with Lewy bodies should be included in the differential diagnosis in individuals presenting w...
Rapidly progressive dementia (RPD) is a rare presentation of different neurological disorders charac...
Background: Creutzfeldt-Jakob disease (CJD) is a prion disease characterized by misfolded proteins t...
Neuropathological diagnostic criteria for Creutzfeldt-Jakob disease (CJD) and other human transmissi...
Introduction: The disease course of dementia with Lewy bodies (DLB) can be rapidly progressive, clin...
Human prion diseases are sometimes difficult to diagnose because few clinical features distinguish t...
OBJECTIVES: To analyse the neuropathological changes behind clinically defined dementia with Lewy bo...
International audienceBackground: Few patients are reported with dementia with Lewy bodies before fi...
Recent neuropathologic autopsy studies found that 15 to 25% of elderly demented patients have Lewy b...
A 75-year-old female with rapidly progressive dementia, pyramidal and extrapyramidal signs, myoclonu...
Chronic Creutzfeldt-Jakob disease, presenting in later life, m a y be difficult to distinguish from ...
The pathologic substrate of the clinical syndrome of dementia with Lewy bodies (DLB) remains to be d...
The spectrum of Lewy body disorders includes not only Parkinson's disease, dementia with Lewy bodies...
Lewy body dementias are the second most common neurodegenerative dementias after Alzheimer's disease...
Rapidly progressive dementia is a curious and elusive clinical description of a pattern of cognitive...
Neuropathologic confirmation of dementia with Lewy bodies (DLB) involves labeling cytoplasmic Lewy b...
Rapidly progressive dementia (RPD) is a rare presentation of different neurological disorders charac...
Background: Creutzfeldt-Jakob disease (CJD) is a prion disease characterized by misfolded proteins t...
Neuropathological diagnostic criteria for Creutzfeldt-Jakob disease (CJD) and other human transmissi...
Introduction: The disease course of dementia with Lewy bodies (DLB) can be rapidly progressive, clin...
Human prion diseases are sometimes difficult to diagnose because few clinical features distinguish t...
OBJECTIVES: To analyse the neuropathological changes behind clinically defined dementia with Lewy bo...
International audienceBackground: Few patients are reported with dementia with Lewy bodies before fi...
Recent neuropathologic autopsy studies found that 15 to 25% of elderly demented patients have Lewy b...
A 75-year-old female with rapidly progressive dementia, pyramidal and extrapyramidal signs, myoclonu...
Chronic Creutzfeldt-Jakob disease, presenting in later life, m a y be difficult to distinguish from ...
The pathologic substrate of the clinical syndrome of dementia with Lewy bodies (DLB) remains to be d...
The spectrum of Lewy body disorders includes not only Parkinson's disease, dementia with Lewy bodies...
Lewy body dementias are the second most common neurodegenerative dementias after Alzheimer's disease...
Rapidly progressive dementia is a curious and elusive clinical description of a pattern of cognitive...
Neuropathologic confirmation of dementia with Lewy bodies (DLB) involves labeling cytoplasmic Lewy b...
Rapidly progressive dementia (RPD) is a rare presentation of different neurological disorders charac...
Background: Creutzfeldt-Jakob disease (CJD) is a prion disease characterized by misfolded proteins t...
Neuropathological diagnostic criteria for Creutzfeldt-Jakob disease (CJD) and other human transmissi...