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Creutzfeldt-Jakob
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Publications and studies (1022)
- Anti-prion drugs do not improve survival in knock-in models of inherited prion disease. (2023/09/29) ♡
- Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Sporadic Creutzfeldt-Jakob Disease With COVID-19 Infection: A Case Report. (2023/09/22) ♡
- Diagnostic and prognostic value of cerebrospinal fluid SNAP-25 and neurogranin in Creutzfeldt-Jakob disease in a clinical setting cohort of rapidly progressive dementias. (2023/09/08) ♡
- Understanding the key features of the spontaneous formation of bona fide prions through a novel methodology that enables their swift and consistent generation. (2023/09/07) ♡
- 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 presenting as Korsakoff syndrome caused by E196A mutation in PRNP gene: A case report. (2023/09/06) ♡
- The epidemiological and clinical characteristics of patients with young-onset genetic Creutzfeldt-Jakob disease. (2023/09/01) ♡
- Risk of variant Creutzfeldt-Jakob disease in a simulated cohort of Canadian blood donors. (2023/09/01) ♡
- Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Altered properties of amyloidogenic prion protein in genetic Creutzfeldt-Jakob disease with PRNP V180I mutation in response to pentosan polysulfate. (2023/09/01) ♡
- Commentary or editorialiAn expert's opinion or commentary, not new research. Respiratory Changes in Creutzfeldt-Jakob Disease: Biots Like Respiratory Pattern. (2023/09/01) ♡
- Autoimmune Antibodies Positivity in Probable Sporadic Creutzfeldt-Jakob Disease: A Mini-Review of Literature. (2023/09/01) ♡
- Alice in Wonderland Syndrome as a Manifestation of Creutzfeldt-Jakob Disease. (2023/09/01) ♡
- Novel histotypes of sporadic Creutzfeldt-Jakob disease linked to 129MV genotype. (2023/08/31) ♡
- Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Spinocerebellar ataxia-type 34: A case report and brief review of the literature. (2023/08/30) ♡
- Genetic analysis of potential biomarkers and therapeutic targets in neuroinflammation from sporadic Creutzfeldt-Jakob disease. (2023/08/29) ♡
- Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. FDG PET/CT and thyroid biopsy leads to neurosarcoidosis diagnosis. (2023/08/28) ♡
- Low risk of variant Creutzfeldt-Jakob disease transmission from blood transfusions in Aotearoa New Zealand suggests donor exclusion policies can be relaxed. (2023/08/25) ♡
- Efficacy of Wex-cide 128 disinfectant against multiple prion strains. (2023/08/24) ♡
- Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. 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. (2023/08/23) ♡
- Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Case report: Creutzfeldt-Jakob disease presenting with anxiety symptoms in a COVID-19 post-infection patient. (2023/08/07) ♡
- 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 Presentation of Creutzfeldt-Jakob Disease as a Stroke Mimic: Experience From an Irish Tertiary Center. (2023/08/07) ♡
- Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Rapidly evolving Creutzfeldt-Jakob disease in COVID-19: from early status epilepticus to fatal outcome. (2023/08/01) ♡
- Sleep in Gerstmann-Straussler-Scheinker disease. (2023/08/01) ♡
- Prevalence of blood donation eligibility in Australia: A population survey. (2023/08/01) ♡
- Using Catchment Population to Estimate Sporadic Creutzfeldt-Jakob Disease Incidence. (2023/07/22) ♡
- Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Misdiagnosis of rarest subtype of sporadic Creutzfeldt Jakob Disease: a case report. (2023/07/18) ♡
- Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Case report: Creutzfeldt-Jakob disease: a case that initiated with the onset of obsessive-compulsive state. (2023/07/18) ♡
- Systematic reviewiAll research on one question is searched according to fixed rules and compared side by side, so that no studies with poor outcomes are missed. Treating cognitive impairments in primary central nervous system infections: A systematic review of pharmacological interventions. (2023/07/14) ♡
- Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Reduplicative paramnesia as an atypical form of presentation of a Heidenhain variant of Creutzfeldt-Jakob disease: A case report. (2023/07/01) ♡
- Caregiver Experiences Navigating the Diagnostic Journey in a Rapidly Progressing Dementia. (2023/07/01) ♡
- Real-time quaking-induced conversion assay using a small-scale substrate production workflow for the diagnosis of Creutzfeldt-Jakob disease. (2023/07/01) ♡
- The role of environmental factors on sporadic Creutzfeldt-Jakob disease mortality: evidence from an age-period-cohort analysis. (2023/07/01) ♡
- Correction: A novel subtype of sporadic Creutzfeldt-Jakob disease with PRNP codon 129MM genotype and PrP plaques. (2023/07/01) ♡
- Toward an early clinical diagnosis of MM2-type sporadic Creutzfeldt-Jakob disease. (2023/07/01) ♡
- 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. Human prion disease: molecular pathogenesis, and possible therapeutic targets and strategies. (2023/07/01) ♡
- Commentary or editorialiAn expert's opinion or commentary, not new research. Bovine Spongiform Encephalopathy, "Mad Cow's Disease" and Variant Creutzfeldt-Jakob Disease in Humans: A Critical Update. (2023/07/01) ♡
- 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. The advances in the early and accurate diagnosis of Creutzfeldt-Jakob disease and other prion diseases: where are we today? (2023/07/01) ♡
- Familial Creutzfeldt-Jakob Disease with early onset myoclonus: A case for fulminant progression. (2023/07/01) ♡
- 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. Transmission of Variant Creutzfeldt-Jakob Disease Through Blood Transfusion and Plasma-Derived Products: A Narrative Review of Observed and Modeled Risks. (2023/07/01) ♡
- Paper-based lateral flow assay for the point-of-care detection of neurofilament light chain. (2023/07/01) ♡
- Kinetics of Abnormal Prion Protein in Blood of Transgenic Mice Experimentally Infected by Multiple Routes with the Agent of Variant Creutzfeldt-Jakob Disease. (2023/06/28) ♡
- Creutzfeldt-Jakob disease surveillance in Australia: update to 31 December 2022. (2023/06/26) ♡
- Correction: The natural history study of preclinical genetic Creutzfeldt-Jakob Disease (CJD): a prospective longitudinal study protocol. (2023/06/13) ♡
- Clinical trialiResearch in patients, without randomization between groups. Useful, but less certain than a randomized trial. Comparative evaluation of clinical and cerebrospinal fluid biomarker characteristics in rapidly and non-rapidly progressive Alzheimer's disease. (2023/06/08) ♡
- Establishing a committee for antemortem reviews of suspect Creutzfeldt-Jakob disease cases in Ireland. (2023/06/01) ♡
- 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. Iron and Ferroptosis More than a Suspect: Beyond the Most Common Mechanisms of Neurodegeneration for New Therapeutic Approaches to Cognitive Decline and Dementia. (2023/06/01) ♡
- 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. A Theoretical Framework on the Biology of Prion Diseases. (2023/06/01) ♡
- Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. When prion disease Isn't suspected: prion disease as the cause of terminal decline in chronic mixed dementia. (2023/06/01) ♡
- Creutzfeldt-Jakob Disease as a Reason for Neurological Deterioration in a Patient with Acute Lymphoblastic Leukemia after Allogeneic Hematopoietic Stem Cell Transplantation. (2023/05/29) ♡
- Kuru. (2023/05/29) ♡
- Systematic reviewiAll research on one question is searched according to fixed rules and compared side by side, so that no studies with poor outcomes are missed. Neutral theory: applicability and neutrality of clinical study endpoints where a disease-specific instrument is available. (2023/05/20) ♡
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