ObjectivesTo identify the misdiagnoses of patients with sporadic Jakob-Creutzfeldt disease (sCJD) during the course of their disease and determine which medical specialties saw patients with sCJD prior to the correct diagnosis being made and at what point in the disease course a correct diagnosis was made.DesignRetrospective medical record review.SettingA specialty referral center of a tertiary academic medical center.ParticipantsOne hundred sixty-three serial patients over a 5.5-year period who ultimately had pathologically proven sCJD. The study used the subset of 97 patients for whom we had adequate medical records.Main outcome measuresOther diagnoses considered in the differential diagnosis and types of medical specialties assessing pat...
Objectives—During an epidemiological study of Creutzfeldt-Jakob disease in Ger-many, Hashimoto’s enc...
Chronic Creutzfeldt-Jakob disease, presenting in later life, m a y be difficult to distinguish from ...
Creutzfeldt-Jakob disease (CJD) belongs to prion diseases (transmissible spongiform encephalopathies...
ObjectivesTo identify the misdiagnoses of patients with sporadic Jakob-Creutzfeldt disease (sCJD) du...
Creutzfeldt-Jakob disease (CJD) is a spongiform encephalopathy with the fatal outcome, caused by the...
Rapidly progressive dementia (RPD) is a rare presentation of different neurological disorders charac...
Rapidly progressive dementia (RPD) is a rare presentation of different neurological disorders charac...
<p>Creutzfeldt-Jakob disease (CJD) is a rare and fatal neurodegenerative disease of unknown ca...
Creutzfeldt-Jakob Disease (CJD) is characterised by subacute progressive dementia, cerebellar ataxi...
Background: Creutzfeldt-Jakob disease (CJD) is a prion disease characterized by misfolded proteins t...
Introduction: Sporadic Creutzfeldt-Jakob disease (sCJD) is a transmissible disorder of the central n...
Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/66084/1/j.1600-0404.1968.tb07440.x.pd
Creutzfeldt-Jakob disease (CJD) is a rare and fatal neurodegenerative disease of unknown cause. Pati...
A 75-year-old female with rapidly progressive dementia, pyramidal and extrapyramidal signs, myoclonu...
Pathological diagnosis remains the gold standard for the diagnosis of sporadic Creutzfeldt-Jakob dis...
Objectives—During an epidemiological study of Creutzfeldt-Jakob disease in Ger-many, Hashimoto’s enc...
Chronic Creutzfeldt-Jakob disease, presenting in later life, m a y be difficult to distinguish from ...
Creutzfeldt-Jakob disease (CJD) belongs to prion diseases (transmissible spongiform encephalopathies...
ObjectivesTo identify the misdiagnoses of patients with sporadic Jakob-Creutzfeldt disease (sCJD) du...
Creutzfeldt-Jakob disease (CJD) is a spongiform encephalopathy with the fatal outcome, caused by the...
Rapidly progressive dementia (RPD) is a rare presentation of different neurological disorders charac...
Rapidly progressive dementia (RPD) is a rare presentation of different neurological disorders charac...
<p>Creutzfeldt-Jakob disease (CJD) is a rare and fatal neurodegenerative disease of unknown ca...
Creutzfeldt-Jakob Disease (CJD) is characterised by subacute progressive dementia, cerebellar ataxi...
Background: Creutzfeldt-Jakob disease (CJD) is a prion disease characterized by misfolded proteins t...
Introduction: Sporadic Creutzfeldt-Jakob disease (sCJD) is a transmissible disorder of the central n...
Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/66084/1/j.1600-0404.1968.tb07440.x.pd
Creutzfeldt-Jakob disease (CJD) is a rare and fatal neurodegenerative disease of unknown cause. Pati...
A 75-year-old female with rapidly progressive dementia, pyramidal and extrapyramidal signs, myoclonu...
Pathological diagnosis remains the gold standard for the diagnosis of sporadic Creutzfeldt-Jakob dis...
Objectives—During an epidemiological study of Creutzfeldt-Jakob disease in Ger-many, Hashimoto’s enc...
Chronic Creutzfeldt-Jakob disease, presenting in later life, m a y be difficult to distinguish from ...
Creutzfeldt-Jakob disease (CJD) belongs to prion diseases (transmissible spongiform encephalopathies...