Neuropsychiatric symptoms in sporadic Creutzfeldt-Jakob disease
Objective: The objective of our study was to assess prospectively the neuropsychiatric features in sCJD (and their impact on caregivers) and compare them with five…Gerstmann-Sträussler-Scheinker disease presenting as dystonia
Objective: Gerstmann-Sträussler-Scheinker disease (GSS) is a type of human transmissible spongiform encephalopathy that is determined genetically. Background: Gerstmann-Sträussler-Scheinker disease (GSS) is a type of human…Gait ataxia and Autonomic dysfunction as early signs of Creutzfeldt-Jakob Disease: A Case Report
Objective: To highlight unusual early presenting symptoms of Sporadic Creutzfeldt-Jakob Disease (sCJD). Background: Prion diseases, a group of rare and fatal diseases caused by an…Sleep-wake disturbance in Creutzfeldt-Jakob disease mimicking fatal familial insomnia
Objective: To report a patient with sleep-wake disturbance mimicking fatal familial insomnia Background: Sleep disturbances are well recognized in fatal familial insomnia (FFI) which is…Functional neurological symptoms as initial presentation of Creutzfeldt-Jacob Disease: case series.
Objective: To describe a clinical series of three patients who presented positive signs of a Functional Movement Disorder (FMD) at the onset of a sporadic…Eyelid opening apraxia as the first manifestation of Creutzfeldt- Jakob disease with 99mTc-TRODAT-1 brain SPECT study
Objective: Our objective is to report a case of sporadic CJD (CJD) in a 57-years-old male patient. It started with severe insomnia followed by eyelid…Gerstmann-Sträussler-Scheinker disease presenting as a late onset slowly progressive spinocerebellar ataxia: expanding the phenotypic spectrum of genetic prion disease
Objective: We describe a late-onset presentation of Gerstmann-Sträussler-Scheinker disease (GSS) with a novel mutation in the prion protein (PRNP) gene. We compare this case to…Predicting Longitudinal Atrophy in Parkinson’s Disease using SIR model
Objective: To predict longitudinal brain changes in Parkinson's disease (PD) using an agent-based model. Background: Considerable evidence suggests that α-synuclein(α-syn) behaves in a prion-like fashion,…Creutzfeldt-Jakob disease with a M232R substitution (CJD232) masquerading as parkinson look-alike syndrome
Objective: To describe a case of Creutzfeldt-Jakob disease with a M232R substitution (CJD 232) presented with parkinson look-alike syndrome and showed remarkably long survival time.…Creutzfeld Jacob disease presenting with functional-appearing, bizarre movements without significant cognitive impairment
Objective: To report unusual presentation of Creutzfeld Jacob disease (CJD) with bizarre movements and functional characteristics. Background: Prion disease is most commonly due to CJD…
Abstracts from the International Congress of Parkinson’s and Movement Disorders.