Creutzfeldt-Jakob
Would you like to receive a message when there is new research on Creutzfeldt-Jakob? This is possible with an account. Create a free account or log in.
Automatically tracked from PubMed and ClinicalTrials.gov, newest on top. Nothing ever disappears here: what you keep in your favorites remains findable. · RSS feed of this disease · only the strongest evidence
Read in plain language what each study is about? With Premium, above each publication you'll find one sentence explaining what was studied — and you'll receive a message as soon as there is new research on Creutzfeldt-Jakob. View what Premium costs.
Publications and studies (1022)
- Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Sporadic Creutzfeldt-Jakob Disease: A Rare Case of Rapid Progressive Cognitive Decline with Special Reference to Magnetic Resonance Spectroscopy. (2024/11/01) ♡
- Upbeat Nystagmus Associated with the Heidenhain Variant of Creutzfeldt-Jakob Disease. (2024/11/01) ♡
- Longitudinal detection of prion infection in preclinical sheep blood samples compared using 3 assays. (2024/10/31) ♡
- A Retrospective Cohort Study of a Newly Proposed Criteria for Sporadic Creutzfeldt-Jakob Disease. (2024/10/30) ♡
- Characterization of Laboratory-Confirmed Creutzfeldt-Jakob Disease From 3 Ontario Tertiary Care Centers Between 2012 and 2022: A Retrospective Cohort Study. (2024/10/28) ♡
- Neuronal Intranuclear Inclusion Disease Presenting with Acute-Onset Dementia and Cortical Edema: A Case Report. (2024/10/28) ♡
- Evaluation of LC3-II Release via Extracellular Vesicles in Relation to the Accumulation of Intracellular LC3-positive Vesicles. (2024/10/18) ♡
- Abnormal synaptic architecture in iPSC-derived neurons from a multi-generational family with genetic Creutzfeldt-Jakob disease. (2024/10/08) ♡
- Reactive microglia partially envelop viable neurons in prion diseases. (2024/10/03) ♡
- Striking intraneuronal neurofilament inclusions restricted to the locus coeruleus in a patient with Creutzfeldt-Jakob disease. (2024/10/02) ♡
- Insufficient evidence for an association between iatrogenic Alzheimer's disease and cadaveric pituitary-derived growth hormone. (2024/10/01) ♡
- "One a penny, two a penny", I saw the hot cross bun sign". (2024/10/01) ♡
- Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Creutzfeldt-Jakob disease: From presentation to palliative care. (2024/10/01) ♡
- Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. An 8-Year 5-Month-Old Boy with a Basal Ganglia Lesion with Triphasic Waves on Electroencephalogram. (2024/10/01) ♡
- Review articleiA summary of what is known about a topic, written by experts. Not compiled according to fixed search rules, so the selection of studies may be biased. Beta-Amyloid Related Neurodegenerative and Neurovascular Diseases: Potential Implications for Transfusion Medicine. (2024/10/01) ♡
- Dopaminergic neurodegeneration in Gerstmann-Sträussler-Scheinker (P102L) disease: insights from imaging and pathological examination. (2024/09/23) ♡
- Review articleiA summary of what is known about a topic, written by experts. Not compiled according to fixed search rules, so the selection of studies may be biased. A Systematic Review of Sporadic Creutzfeldt-Jakob Disease: Pathogenesis, Diagnosis, and Therapeutic Attempts. (2024/09/20) ♡
- Optimizing Corneal Transplant Safety: The Impact of Mandatory Prion Protein Testing on Iatrogenic Creutzfeldt-Jakob Disease Prevention in the Czech Republic. (2024/09/18) ♡
- Involvement of the nigrostriatal system in Gerstman-Sträussler-Scheinker disease with the PRNP-P102L mutation. (2024/09/15) ♡
- Prion diseases disrupt glutamate/glutamine metabolism in skeletal muscle. (2024/09/11) ♡
- Clinical, neuropathological, and molecular characteristics of rapidly progressive dementia with Lewy bodies: a distinct clinicopathological entity? (2024/09/10) ♡
- Screening of Anti-Prion Compounds Using the Protein Misfolding Cyclic Amplification Technology. (2024/09/04) ♡
- Laboratory or animal researchiNo research in humans yet. Promising in a test tube or in mice unfortunately means nothing for patients. Lack of prion transmission barrier in human PrP transgenic Drosophila. (2024/09/01) ♡
- Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Creutzfeldt-Jakob disease in a heterozygous GBA mutation carrier: Coincidence or consequence? (2024/09/01) ♡
- Familial Creutzfeldt-Jakob Disease (CJD) Kindred - An Unusual Case Report from India. (2024/09/01) ♡
- Review articleiA summary of what is known about a topic, written by experts. Not compiled according to fixed search rules, so the selection of studies may be biased. Creutzfeldt-Jakob disease presenting as psychiatric disorder: case presentation and systematic review. (2024/08/29) ♡
- Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Heidenhain Variant of Creutzfeldt-Jakob Disease: A Case Report. (2024/08/26) ♡
- Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Parkinsonism as an initial presentation of Creutzfeldt-Jakob disease: A case report and review of literature. (2024/08/10) ♡
- Syntaxin-6 delays prion protein fibril formation and prolongs the presence of toxic aggregation intermediates. (2024/08/07) ♡
- Adaptation of the protein misfolding cyclic amplification (PMCA) technique for the screening of anti-prion compounds. (2024/07/31) ♡
- Creutzfeldt-Jakob Disease and Fatal Familial Insomnia: Demographics and In-Hospital Mortality in Spain. (2024/07/27) ♡
- Genome wide association study of clinical duration and age at onset of sporadic CJD. (2024/07/26) ♡
- 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. (2024/07/25) ♡
- Review articleiA summary of what is known about a topic, written by experts. Not compiled according to fixed search rules, so the selection of studies may be biased. Clinical Application of Blood Biomarkers in Neurodegenerative Diseases-Present and Future Perspectives. (2024/07/25) ♡
- Neuropathologically directed profiling of PRNP somatic and germline variants in sporadic human prion disease. (2024/07/24) ♡
- Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. An Atypical Case of Creutzfeldt-Jakob Syndrome Presenting with Cacosmia and Amyloid Positivity. (2024/07/23) ♡
- Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Atypical Presentation of Probable Sporadic Creutzfeldt-Jakob Disease: A Patient Without Mental Deterioration. (2024/07/18) ♡
- 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). (2024/07/15) ♡
- Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Sporadic Creutzfeldt-Jakob Disease: Finding the Needle in the Haystack. (2024/07/15) ♡
- Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Unusually Late Onset of Creutzfeldt-Jakob Disease Following COVID-19 Infection in India: A Case Report. (2024/07/02) ♡
- A nested cross validation approach to machine learning model performance evaluation on a small dataset for Creutzfeldt-Jakob disease diagnosis. (2024/07/01) ♡
- Comprehensive Analysis of Dementia Types and Risk Factors: A Study From a Tertiary Care Center in India. (2024/06/20) ♡
- Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Dysarthria as a Presenting Symptom With Rapidly Progressive Imaging Features in Sporadic Creutzfeldt-Jakob Disease: A Case Report. (2024/06/19) ♡
- Modelling hepatitis C infection acquired from blood transfusions in the UK between 1970 and 1991 for the Infected Blood Inquiry. (2024/06/05) ♡
- Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Sporadic Creutzfeldt Jakob disease: Case series in Peru. (2024/03/30) ♡
- Enhanced Creutzfeldt-Jakob disease surveillance in the older population: Assessment of a protocol for screening brain tissue donations for prion disease. (2024/03/01) ♡
- Sensory disturbances in Creutzfeldt-Jakob disease. (2024/03/01) ♡
- Commentary or editorialiAn expert's opinion or commentary, not new research. Dynamic diffusion imaging changes and unique midbrain involvement in a probable MV2K sCJD. (2024/03/01) ♡
- Commentary or editorialiAn expert's opinion or commentary, not new research. Rapidly progressive dementia with focal symptoms: when to suspect Creutzfeldt-Jakob disease? (2024/02/01) ♡
- Personalized brain MRI revealed distinct functional and anatomical disruptions in Creutzfeldt-Jakob disease and Alzheimer's disease. (2024/02/01) ♡
codex.care does not provide medical advice. Always discuss symptoms, medication, and treatment choices with your own healthcare provider.