Disease: Variant Creutzfeldt-Jakob disease
- "One a penny, two a penny", I saw the hot cross bun sign"
- A review of the enhanced CJD surveillance feasibility study in the elderly in Scotland, UK
- A systemic analysis of Creutzfeldt Jakob disease cases in Asia
- A Theoretical Framework on the Biology of Prion Diseases
- Absence of evidence of transfusion transmission risk of Creutzfeldt-Jakob disease in the United States: Results froma 28-year lookback study
- Advancing surgical instrument safety: A screen of oxidative and alkaline prion decontaminants using real-time quaking-induced conversion with prion-coated steel beads as surgical instrument mimetic
- Alice in Wonderland Syndrome as a Manifestation of Creutzfeldt-Jakob Disease
- Altered properties of amyloidogenic prion protein in genetic Creutzfeldt-Jakob disease with PRNP V180I mutation in response to pentosan polysulfate
- Anti-prion drugs do not improve survival in novel knock-in models of inherited prion disease
- Assessing the risk of transfusion-transmitted variant Creutzfeldt-Jakob disease: a European perspective
- Assessing the risk of transfusion-transmitted variant Creutzfeldt-Jakob disease: an European perspective
- Assessment of the Zoonotic Potential of Atypical Scrapie Prions in Humanized Mice Reveals Rare Phenotypic Convergence but Not Identity With Sporadic Creutzfeldt-Jakob Disease Prions
- Change in Epidemiology of Creutzfeldt-Jakob Disease in the US, 2007-2020
- Characterisation and prion transmission study in mice with genetic reduction of sporadic Creutzfeldt-Jakob disease risk gene Stx6
- Clinical characteristics and diagnostics of human spongiform encephalopathies: an update
- Comprehensive Analysis of Dementia Types and Risk Factors: A Study From a Tertiary Care Center in India
- Concerns and Considerations: Creutzfeldt-Jakob Disease in Pakistan and Reusable Laryngoscopes
- Creutzfeldt-Jakob Disease and other prion diseases
- Creutzfeldt-Jakob disease in a man surviving COVID-19: disentangling a casual or causal association by neuropathology
- Creutzfeldt-Jakob disease presenting as Korsakoff syndrome caused by E196A mutation in <em>PRNP</em> gene: A case report
- Detection limitations of prion seeding activities in blood samples from patients with sporadic prion disease
- Detection of prions in matching post-mortem skin and cerebrospinal fluid samples using second-generation real-time quaking-induced conversion assay
- Development of a sensitive real-time quaking-induced conversion (RT-QuIC) assay for application in prion-infected blood
- Development of statistical auto-segmentation method for diffusion restriction gray matter lesions in patients with newly diagnosed sporadic Creutzfeldt-Jakob disease
- Diagnostic accuracy of diffusion-weighted imaging in variant Creutzfeldt-Jakob disease
- Diagnostic and prognostic value of cerebrospinal fluid SNAP-25 and neurogranin in Creutzfeldt-Jakob disease in a clinical setting cohort of rapidly progressive dementias
- Diagnostic and Prognostic Value of Plasma GFAP in Sporadic Creutzfeldt-Jakob Disease in the Clinical Setting of Rapidly Progressive Dementia
- Diagnostic challenge of Creutzfeldt-Jakob disease in a patient with multimorbidity: a case-report
- Effect of SARS-CoV-2 Incidence and Immunisation Rates on Sporadic Creutzfeldt-Jakob Disease Incidence
- Efficacy of Wex-cide 128 disinfectant against multiple prion strains
- Elevated E200K Somatic Mutation of the Prion Protein Gene (<em>PRNP</em>) in the Brain Tissues of Patients with Sporadic Creutzfeldt-Jakob Disease (CJD)
- Enhanced Creutzfeldt-Jakob disease surveillance in the older population: Assessment of a protocol for screening brain tissue donations for prion disease
- Exploring CJD incidence trends: insights from Slovakia
- Genetic analysis of potential biomarkers and therapeutic targets in neuroinflammation from sporadic Creutzfeldt-Jakob disease
- Genetic insights into drug targets for sporadic Creutzfeldt-Jakob disease: Integrative multi-omics analysis
- Genome wide association study of clinical duration and age at onset of sporadic CJD
- Has the frequency of ABO RhD blood groups in Australian blood donors changed as a result of the removal of the variant Creutzfeldt-Jakob disease-based deferral?
- Heidenhain variant of Creutzfeldt-Jakob disease masquerading as neuromyelitis optica spectrum disorder: recognizing when apheresis is not the answer
- Human immunodeficiency virus-associated dementia complex with positive 14-3-3 protein in cerebrospinal fluid: A case report
- Iatrogenic Alzheimer's disease in recipients of cadaveric pituitary-derived growth hormone
- Interactions between Cytokines and the Pathogenesis of Prion Diseases: Insights and Implications
- Isolated Diffuse Precentral Gyrus Signals in Creutzfeldt-Jakob Disease
- Kinetics of Abnormal Prion Protein in Blood of Transgenic Mice Experimentally Infected by Multiple Routes with the Agent of Variant Creutzfeldt-Jakob Disease
- Kuru Disease: Bridging the Gap Between Prion Biology and Human Health
- Large-scale validation of skin prion seeding activity as a biomarker for diagnosis of prion diseases
- Longitudinal detection of prion infection in preclinical sheep blood samples compared using 3 assays
- Low risk of variant Creutzfeldt-Jakob disease transmission from blood transfusions in Aotearoa New Zealand suggests donor exclusion policies can be relaxed
- Magnetic Resonance Imaging Characteristics of LGI1-Antibody and CASPR2-Antibody Encephalitis
- Metabolic Brain Changes Can Predict the Underlying Pathology in Neurodegenerative Brain Disorders: A Case Report of Sporadic Creutzfeldt-Jakob Disease with Concomitant Parkinson's Disease
- Misdiagnosis of rarest subtype of sporadic Creutzfeldt Jakob Disease: a case report
- Modelling hepatitis C infection acquired from blood transfusions in the UK between 1970 and 1991 for the Infected Blood Inquiry
- MRI abnormalities in Creutzfeldt-Jakob disease and other rapidly progressive dementia
- Neural cell engraftment therapy for sporadic Creutzfeldt-Jakob disease restores neuroelectrophysiological parameters in a cerebral organoid model
- Neuropathologically directed profiling of PRNP somatic and germline variants in sporadic human prion disease
- Neuropathologically-directed profiling of PRNP somatic and germline variants in sporadic human prion disease
- New Light on Prions: Putative Role of PrP<sup>c</sup> in Pathophysiology of Mood Disorders
- Non-convulsive status epilepticus versus periodic EEG pattern in sporadic Creutzfeldt-Jakob disease: two sides of the same coin?
- Nonconvulsive status epilepticus versus periodic EEG pattern in sporadic Creutzfeldt-Jakob disease: two sides of the same coin?
- Novel diagnostic and prognostic approach for rapidly progressive dementias: Indicators based on amyloid/tau/neurodegeneration (ATN) framework
- Novel histotypes of sporadic Creutzfeldt-Jakob disease linked to 129MV genotype
- Novel method for classification of prion diseases by detecting PrP<sup>res</sup> signal patterns from formalin-fixed paraffin-embedded samples
- Pathology of neurodegenerative disease for the general neurologist
- Perceived Fluctuation of MRI Findings in a Prolonged Course of the Heidenhain Variant of Creutzfeldt-Jakob Disease
- Performance of a seed amplification assay for misfolded alpha-synuclein in cerebrospinal fluid and brain tissue in relation to Lewy body disease stage and pathology burden
- Ping-Pong Gaze in Sporadic Creutzfeldt-Jakob Disease
- Pooled analysis of patients with inherited prion disease caused by two- to twelve-octapeptide repeat insertions in the prion protein gene (PRNP)
- Prediction of clinical progression in nervous system diseases: plasma glial fibrillary acidic protein (GFAP)
- Prevalence of blood donation eligibility in Australia: A population survey
- Prion diseases, always a threat?
- Prion meeting 2023: implications of a growing field
- Prion science and its unsung heroes
- Prospective 25-year surveillance of prion diseases in France, 1992 to 2016: a slow waning of epidemics and an increase in observed sporadic forms
- Punctate Diffuse Cortex Signals in Creutzfeldt-Jakob Disease
- Rapid progression of probable Creutzfeldt-Jakob disease with concomitant COVID-19 infection
- Rapidly Progressive Dementia in an Elderly Male: Perseverance Becomes the Key to a Rare Diagnosis
- Removal of UK-donor deferral for variant Creutzfeldt-Jakob disease: A large donation gain in Australia
- Respıratuar Changes ın Creutzfeldt-Jakob Dısease: Bıot Lıke Respıratuar Pattern
- Review of a series of cases of Creutzfeldt-Jakob disease in a tertiary care hospital
- Risk of variant Creutzfeldt-Jakob disease in a simulated cohort of Canadian blood donors
- Roving Eye and Head in a Patient With Genetic Creutzfeldt-Jakob Disease
- Spinocerebellar ataxia-type 34: A case report and brief review of the literature
- Spontaneous prion disease in homozygous and heterozygous transgenic mouse models of T188K genetic Creutzfeldt-Jakob disease
- Sporadic Creutzfeldt-Jakob disease in adults over 80 years: a 10-year review of United Kingdom surveillance
- Sporadic Creutzfeldt-Jakob Disease Initially Presenting With Posterior Reversible Encephalopathy Syndrome: A Case Report
- Sporadic Creutzfeldt-Jakob Disease With Slow Progression:Report of One Case
- Systematic approach to diagnosing suspected Creutzfeldt-Jakob disease
- The advances in the early and accurate diagnosis of Creutzfeldt-Jakob disease and other prion diseases: where are we today?
- The Etiology of Rapidly Progressive Dementia: A 3-Year Retrospective Study in a Tertiary Hospital in China
- The Psychiatric Presentation of Creutzfeldt-Jakob Disease
- The rapid progression of Creutzfeldt-Jakob disease with concomitant COVID-19 infection: a case report
- The rapid progression of Creutzfeldt-Jakob disease with concomitant COVID-19 infection: a case report
- The Role of PET Imaging in Patients with Prion Disease: A Literature Review
- Transfusion Transmitted Disease
- Transmission of Variant Creutzfeldt-Jakob Disease Through Blood Transfusion and Plasma-Derived Products: A Narrative Review of Observed and Modeled Risks
- Two Chinese patients of sporadic Creutzfeldt-Jacob disease with a S97N mutation in <em>PRNP</em> gene
- Understanding Creutzfeldt-Jakob disease in Iran: a systematic review of case reports
- Understanding the key features of the spontaneous formation of bona fide prions through a novel methodology that enables their swift and consistent generation
- Updated global epidemiology atlas of human prion diseases
- Variably protease-sensitive prionopathy with methionine homozygosity at codon 129 in the prion protein gene
- When prion disease Isn't suspected: prion disease as the cause of terminal decline in chronic mixed dementia