Disease: Creutzfeldt-Jakob disease
- A Devastating Neurological Disorder: Anti-Dipeptidyl-Peptidase-Like Protein 6 (DPPX) Encephalitis Causing Rapidly Progressive Dementia
- A review of the enhanced CJD surveillance feasibility study in the elderly in Scotland, UK
- A Study of Clinical Profile, Radiological and Electroencephalographic Characteristics of Sporadic Creutzfeldt-Jakob Disease From a Tertiary Care Hospital
- 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
- Addressing the Unmet Needs of Patients With Rapidly Progressive Neurological Disease: A Case Report of Palliative Care in Creutzfeldt-Jakob Disease (CJD)
- Alice in Wonderland Syndrome as a Manifestation of Creutzfeldt-Jakob Disease
- 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
- Assessment of the zoonotic potential of atypical scrapie prions in humanized mice reveals rare phenotypic convergence but not identity with sporadic CJD prions
- Autoimmune Antibodies Positivity in Probable Sporadic Creutzfeldt-Jakob Disease: A Mini-Review of Literature
- Brain Organoids: A Game-Changer for Drug Testing
- 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
- Characterisation of RT-QuIC negative cases from the UK National CJD Research and Surveillance programme
- Clinical characteristics and diagnostics of human spongiform encephalopathies: an update
- Creutzfeldt Jakob Disease
- 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: A Rare Case of Dementia
- CSF 14-3-3beta is associated with progressive cognitive decline in Alzheimer's disease
- CSF 14-3-3β is associated with progressive cognitive decline in Alzheimer's disease
- 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
- Different reactive profiles of calmodulin in the CSF samples of Chinese patients of four types of genetic prion diseases
- Dynamic diffusion imaging changes and unique midbrain involvement in a probable MV2K sCJD
- Effect of SARS-CoV-2 Incidence and Immunisation Rates on Sporadic Creutzfeldt-Jakob Disease Incidence
- Efficient transmission of human prion diseases to a glycan-free prion protein-expressing host
- Electroencephalography in encephalopathy and encephalitis
- Elevated E200K Somatic Mutation of the Prion Protein Gene (<em>PRNP</em>) in the Brain Tissues of Patients with Sporadic Creutzfeldt-Jakob Disease (CJD)
- Elevated E200K Somatic Mutation of the Prion Protein Gene (PRNP) in the Brain Tissues of Patients with Sporadic Creutzfeldt-Jakob Disease (CJD)
- Eye Catching Advancement for Creutzfeldt-Jakob Disease Diagnostics
- Fractal Analysis in Neurodegenerative Diseases
- Genetic and pathological features encipher the phenotypic heterogeneity of Gerstmann-Straussler-Scheinker disease
- Geographic Diversity in the Incidence of Human Prion Diseases - China, 2006-2019
- 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
- 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
- Human prion diseases and the prion protein - what is the current state of knowledge?
- 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
- 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
- Levels of plasma brain-derived tau and p-tau181 in Alzheimer's disease and rapidly progressive dementias
- Magnetic resonance imaging arterial spin labeling hypoperfusion with diffusion-weighted image hyperintensity is useful for diagnostic imaging of Creutzfeldt-Jakob disease
- Magnetic Resonance Imaging Characteristics of LGI1-Antibody and CASPR2-Antibody Encephalitis
- Multidimensional features of sporadic Creutzfeldt-Jakob disease in the elderly: a case report and systematic review
- Neural cell engraftment therapy for sporadic Creutzfeldt-Jakob disease restores neuroelectrophysiological parameters in a cerebral organoid model
- Neuropathology of the Neurodegenerative Diseases
- New implications for prion diseases therapy and prophylaxis
- 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 method for classification of prion diseases by detecting PrP<sup>res</sup> signal patterns from formalin-fixed paraffin-embedded samples
- Paper-based lateral flow assay for the point-of-care detection of neurofilament light chain
- Pathology of neurodegenerative disease for the general neurologist
- 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
- Perioperative concerns in a patient with suspected Creutzfeldt - Jakob disease: A case report and review of literature
- Ping-Pong Gaze in Sporadic Creutzfeldt-Jakob Disease
- Potential Therapeutic Use of Stem Cells for Prion Diseases
- Prediction of clinical progression in nervous system diseases: plasma glial fibrillary acidic protein (GFAP)
- Primary progressive aphasia with focal periodic sharp wave complexes: An unusual manifestation of Creutzfeldt-Jakob disease
- Prion meeting 2023: implications of a growing field
- Prion science and its unsung heroes
- Probable Sporadic Creutzfeldt-Jakob Disease Presenting as Refractory Status Epilepticus in a Poststroke Epilepsy Patient: A Case Report
- Progressive supranuclear palsy phenotype as an atypical clinical presentation of Creutzfeldt-Jakob disease: A case report and review of the literature
- Proliferation of mesaxons in the optic nerve of hamsters infected with the Echigo-l strain of Creutzfeldt-Jakob disease
- 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
- Respiratuar Changes in Creutzfeldt-Jakob Disease: Biot Like Respiratuar Pattern
- 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
- 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
- Short incubation periods of atypical H-type BSE in cattle with EK211 and KK211 prion protein genotypes after intracranial inoculation
- Slow to Respond: A Rapidly Progressive Case of Sporadic Creutzfeldt-Jakob Disease
- Sporadic Creutzfeldt-Jakob Disease With COVID-19 Infection: A Case Report
- Sporadic Creutzfeldt-Jakob Disease With Slow Progression:Report of One Case
- Sporadic Creutzfeldt-Jakob disease: Brain MRI lesion features from 2 cases reports
- Systematic approach to diagnosing suspected 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
- Two Chinese patients of sporadic Creutzfeldt-Jacob disease with a S97N mutation in <em>PRNP</em> gene
- Two Chinese patients of sporadic Creutzfeldt-Jacob disease with a S97N mutation in PRNP gene
- Use of Tumguide in the Insertion of a Nasogastric Tube Into the Stomach of a Patient With Creutzfeldt-Jakob Disease in a Nursing Home: A Case Report
- Use of Tumguide® in the Insertion of a Nasogastric Tube Into the Stomach of a Patient With Creutzfeldt-Jakob Disease in a Nursing Home: A Case Report
- Validation of the Medical Research Council prion disease rating scale in France
- 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
- Αnti-prion effects of anthocyanins