• "One a penny, two a penny", I saw the hot cross bun sign"
• 18F-FDG PET/CT in early phase of sporadic Creutzfeldt-Jacob disease: A case report
• A Comparison of RML Prion Inactivation Efficiency by Heterogeneous and Homogeneous Photocatalysis
• A Devastating Neurological Disorder: Anti-Dipeptidyl-Peptidase-Like Protein 6 (DPPX) Encephalitis Causing Rapidly Progressive Dementia
• A rare case of Sporadic Creutzfeldt-Jakob disease at a remote mountain hospital in the Indian Himalayan Region
• A systemic analysis of Creutzfeldt Jakob disease cases in Asia
• Absence of evidence of transfusion transmission risk of Creutzfeldt-Jakob disease in the United States: Results froma 28-year lookback study
• Adaptation of the protein misfolding cyclic amplification (PMCA) technique for the screening of anti-prion compounds
• Addressing the Unmet Needs of Patients With Rapidly Progressive Neurological Disease: A Case Report of Palliative Care in Creutzfeldt-Jakob Disease (CJD)
• 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
• Alzheimer's disease biomarker utilization at first referral enhances differential diagnostic precision with simultaneous exclusion of Creutzfeldt-Jakob disease
• An autopsy case of MV 2K + C subtype of Creutzfeldt-Jakob disease
• Anti-prion drugs do not improve survival in novel knock-in models of inherited prion disease
• Assessing the newly proposed MRI criteria for diagnosing sporadic creutzfeldt-jakob 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 CJD prions
• 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
• Atypical Presentation of Probable Sporadic Creutzfeldt-Jakob Disease: A Patient Without Mental Deterioration
• Brain Organoids: A Game-Changer for Drug Testing
• Cerebrospinal fluid p-tau181, 217, and 231 in definite Creutzfeldt-Jakob disease with and without concomitant pathologies
• Characterisation of RT-QuIC negative cases from the UK National CJD Research and Surveillance programme
• Clinical Application of Blood Biomarkers in Neurodegenerative Diseases-Present and Future Perspectives
• 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 Fatal Familial Insomnia: Demographics and In-Hospital Mortality in Spain
• Creutzfeldt-Jakob Disease and other prion diseases
• Creutzfeldt-Jakob disease in a man surviving COVID-19: disentangling a casual or causal association by neuropathology
• Dementia With Lewy Bodies Phenocopy in a Case of RT-QuIC-Negative Creutzfeldt-Jakob Disease: Implications of Functional Anatomy
• 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 statistical auto-segmentation method for diffusion restriction gray matter lesions in patients with newly diagnosed sporadic Creutzfeldt-Jakob disease
• Diagnostic and Prognostic Value of Plasma GFAP in Sporadic Creutzfeldt-Jakob Disease in the Clinical Setting of Rapidly Progressive Dementia
• Different reactive profiles of calmodulin in the CSF samples of Chinese patients of four types of genetic prion diseases
• Disulfidoptosis as a Novel Mechanism of Neuronal Death: Insights from Creutzfeldt-Jakob Disease
• Dysarthria as a Presenting Symptom With Rapidly Progressive Imaging Features in Sporadic Creutzfeldt-Jakob Disease: A Case Report
• Euphoric Presentation in Creutzfeldt-Jakob Disease and Its Diagnostic Implications: A Case Report
• Evaluation and Limitations of the Novel Chemiluminescent Enzyme Immunoassay Technique for Measuring Total Tau Protein in the Cerebrospinal Fluid of Patients with Human Prion Disease: A 10-Year Prospective Study (2011-2020)
• Exploring CJD incidence trends: insights from Slovakia
• Exploring the Relationship Between Sporadic Creutzfeldt-Jakob Disease and Gut Microbiota Through a Mendelian Randomization Study
• Fractal Analysis in Neurodegenerative Diseases
• Genetic and pathological features encipher the phenotypic heterogeneity of Gerstmann-Straussler-Scheinker disease
• Genetic characterization of the prion protein gene in camels (Camelus) with comments on the evolutionary history of prion disease in Cetartiodactyla
• 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?
• Hereditary Creutzfeldt-Jakob Disease: A Case Presentation of a Rare Stroke Mimic
• 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
• IgLON5 autoimmunity in a patient with Creutzfeldt-Jakob disease: case report and review of literature
• Infectious Diseases of the Brain and Spine: Parasitic and Other Atypical Transmissible Diseases
• Insufficient evidence for an association between iatrogenic Alzheimer's disease and cadaveric pituitary-derived growth hormone
• Interactions between Cytokines and the Pathogenesis of Prion Diseases: Insights and Implications
• Involvement of the nigrostriatal system in Gerstman-Straussler-Scheinker disease with the PRNP-P102L mutation
• Isolated Diffuse Precentral Gyrus Signals in Creutzfeldt-Jakob Disease
• Kuru Disease: Bridging the Gap Between Prion Biology and Human Health
• Longitudinal detection of prion infection in preclinical sheep blood samples compared using 3 assays
• Magnetic Resonance Imaging Characteristics of LGI1-Antibody and CASPR2-Antibody Encephalitis
• Modelling hepatitis C infection acquired from blood transfusions in the UK between 1970 and 1991 for the Infected Blood Inquiry
• Modulating the aggregation of human prion protein PrP_106-126 by an indole-based cyclometallated palladium complex
• Multidimensional features of sporadic Creutzfeldt-Jakob disease in the elderly: a case report and systematic review
• 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
• Neuropathology of the Neurodegenerative Diseases
• New implications for prion diseases therapy and prophylaxis
• New Light on Prions: Putative Role of PrP^c in Pathophysiology of Mood Disorders
• Novel diagnostic and prognostic approach for rapidly progressive dementias: Indicators based on amyloid/tau/neurodegeneration (ATN) framework
• Novel method for classification of prion diseases by detecting PrP^res signal patterns from formalin-fixed paraffin-embedded samples
• Parkinsonism as an initial presentation of Creutzfeldt-Jakob disease: A case report and review of literature
• Perceived Fluctuation of MRI Findings in a Prolonged Course of the Heidenhain Variant of Creutzfeldt-Jakob Disease
• Perioperative concerns in a patient with suspected Creutzfeldt - Jakob disease: A case report and review of literature
• Post-translational modifications in prion diseases
• Primary progressive aphasia with focal periodic sharp wave complexes: An unusual manifestation of Creutzfeldt-Jakob disease
• Prion diseases, always a threat?
• Prion meeting 2023: implications of a growing field
• Progressive supranuclear palsy phenotype as an atypical clinical presentation of Creutzfeldt-Jakob disease: A case report and review of the literature
• Proliferative arrest induces neuron differentiation and innate immune responses in control and Creutzfeldt-Jakob Disease agent infected rat septal neurons
• Roving Eye and Head in a Patient With Genetic Creutzfeldt-Jakob Disease
• Selective Vulnerability to Neurodegenerative Disease: Insights from Cell Type-Specific Translatome Studies
• Sensitive detection of pathological seeds of α-synuclein, tau and prion protein on solid surfaces
• Slow to Respond: A Rapidly Progressive Case of Sporadic Creutzfeldt-Jakob Disease
• Sporadic Creutzfeldt-Jakob disease in adults over 80 years: a 10-year review of United Kingdom surveillance
• Sporadic Creutzfeldt-Jakob Disease: Finding the Needle in the Haystack
• Syntaxin-6 delays prion protein fibril formation and prolongs presence of toxic aggregation intermediates
• The Etiology of Rapidly Progressive Dementia: A 3-Year Retrospective Study in a Tertiary Hospital in China
• The history of the Japanese Society for Neuro-infectious Diseases: Foundation, objectives, and legacy
• The Importance of Long-term Partner Observation in Cognitive Evaluation: A Very Early Creutzfeldt-Jakob Disease in a Patient with Mild Cognitive Impairment
• The Psychiatric Presentation of Creutzfeldt-Jakob Disease
• 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
• Understanding Creutzfeldt-Jakob disease in Iran: a systematic review of case reports
• Unmet needs of biochemical biomarkers for human prion diseases
• Unusually Late Onset of Creutzfeldt-Jakob Disease Following COVID-19 Infection in India: A Case Report
• Updated global epidemiology atlas of human prion diseases
• Usefulness of minimally invasive autopsy in the diagnosis of arboviruses to increase the sensitivity of the Epidemiological Surveillance System in Ceará, Brazil
• 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
• White matter abnormalities in healthy E200K carriers may serve as an early biomarker for genetic Creutzfeldt-Jakob disease (gCJD)
• Αnti-prion effects of anthocyanins