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Sensory disturbances in Creutzfeldt-Jakob disease
BackgroundCreutzfeldt-Jakob disease (CJD) is a fatal neurodegenerative disease characterized by rapidly progressive dementia, motor impairments, and...
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Early Cortical Diffusion Restriction in Creutzfeldt-Jakob Disease: a Case Report
Creutzfeldt-Jakob disease is a spongiform encephalopathy with rapidly progressing neurological symptoms. Always is there a fatal outcome, usually...
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Application of real-time quaking-induced conversion in Creutzfeldt–Jakob disease surveillance
BackgroundEvaluation of the application of CSF real-time quaking-induced conversion in Creutzfeldt–Jakob disease surveillance to investigate test...
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Acceleration of sporadic Creutzfeldt–Jakob disease progression by COVID requires evidence from appropriately designed studies
The aim of this letter to the editor is to discuss the influence of SARS-CoV-2 infection on the progression of sporadic Creutzfeldt–Jakob disease...
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Diagnostic accuracy of diffusion-weighted imaging in variant Creutzfeldt–Jakob disease
PurposeThis study sought to investigate the diagnostic sensitivity of diffusion-weighted imaging (DWI) in variant Creutzfeldt-Jakob disease (vCJD), a...
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MRI abnormalities in Creutzfeldt–Jakob disease and other rapidly progressive dementia
ObjectiveTo investigate brain MRI abnormalities in a cohort of patients with rapidly progressive dementia (RPD) with and without a diagnosis of...
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Creutzfeldt–Jakob disease and other prion diseases
Prion diseases share common clinical and pathological characteristics such as spongiform neuronal degeneration and deposition of an abnormal form of...
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Diagnostic challenge of Creutzfeldt-Jakob disease in a patient with multimorbidity: a case-report
BackgroundCreutzfeldt-Jakob disease (CJD) is a rapidly progressive and ultimately fatal neurodegenerative condition caused by prions. The clinical...
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Gut microbiota and metabolome in sporadic Creutzfeldt–Jakob disease
BackgroundGut dysbiosis and the resulting changes in the metabolites have been associated with neurological diseases. However, the relationship...
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Creutzfeldt–Jakob disease in a post-COVID-19 patient: did SARS-CoV-2 accelerate the neurodegeneration?
BackgroundCreutzfeldt–Jakob disease (CJD) is a rare, fatal neurodegenerative disorder, with few months as a usual duration from onset to death.
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Creutzfeldt-Jakob disease in a man surviving COVID-19: disentangling a casual or causal association by neuropathology
BackgroundLiterature reporting the onset of Creutzfeldt-Jakob disease (CJD) immediately after COVID-19 infection has strengthened a possible causal...
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Misdiagnosis of rarest subtype of sporadic Creutzfeldt Jakob Disease: a case report
BackgroundCreutzfeldt–Jakob disease (CJD), is a deadly degenerative condition of the central nervous system marked by rapidly progressive dementia....
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Creutzfeldt-Jakob-Krankheit – eine mögliche Differentialdiagnose an einer Psychiatrie
Prion diseases are lethal neurodegenerative diseases that arise through changes in conformation of physiological prion proteins into a pathological...
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Functional neurological symptoms as initial presentation of Creutzfeldt-Jakob disease: case series
BackgroundFunctional Neurological Disorders (FND) are common in clinical practice. It is recognized that FND may present at onset or during the...
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Establishing a committee for antemortem reviews of suspect Creutzfeldt-Jakob disease cases in Ireland
BackgroundCreutzfeldt-Jakob disease (CJD) is a rapidly progressive, neurodegenerative disease. In Ireland, clinical diagnostics and laboratory...
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The role of environmental factors on sporadic Creutzfeldt-Jakob disease mortality: evidence from an age-period-cohort analysis
Sporadic Creutzfeldt-Jakob disease (sCJD) is the most common form of prion diseases. The causes of sCJD are still unknown and exogenous factors may...
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The risk of Creutzfeldt–Jakob disease infection in cadaveric surgical training
The usefulness of cadaver surgical training in the clinical field is already well known. In Japan, the number of universities introducing cadaver...
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Neutrophil to High-density Lipoprotein ratio (NHR) as a potential predictor of disease severity and survival time in Creutzfeldt-Jakob disease
IntroductionCreutzfeldt-Jakob disease (CJD) is a fatal and irreversible neurodegenerative disease. Identification of inexpensive and...
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The natural history study of preclinical genetic Creutzfeldt-Jakob Disease (CJD): a prospective longitudinal study protocol
BackgroundCreutzfeldt-Jakob Disease (CJD) is the most common prion disease in humans causing a rapidly progressive neurological decline and dementia...
