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Creutzfeldt-Jakob

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Search Period All yearsLast 12 monthsLast 5 years Topic All topicsGeneralNutrition and dietAlternative treatment methods Type of research Any type of researchHighest quality evidence only (18)Meta-analysis (4)Systematic review (13)Phase 3 study (1)Clinical trial (24)Review article (145)Early study (phase 1 or 2) (3)Case report (262)Laboratory or animal research (18)Commentary or editorial (48) Studies currently seeking participants only (7)

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Publications and studies (1022)

• Formalin RT-QuIC assay detects prion-seeding activity in formalin-fixed brain samples from sporadic Creutzfeldt-Jakob disease patients. (2021/11/01) ♡
• Commentary or editorialiAn expert's opinion or commentary, not new research. CJD without borders. (2021/11/01) ♡
• The protease-sensitive N-terminal polybasic region of prion protein modulates its conversion to the pathogenic prion conformer. (2021/11/01) ♡
• Creutzfeldt-Jakob Disease in Nonagenarian: A Rare Presentation from India. (2021/11/01) ♡
• 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. Variant CJD: Reflections a Quarter of a Century on. (2021/10/30) ♡
• Commentary or editorialiAn expert's opinion or commentary, not new research. Sporadic Creutzfeldt-Jakob Disease in a Very Young Person. (2021/10/26) ♡
• Commentary or editorialiAn expert's opinion or commentary, not new research. The Intractable Puzzle of Sporadic Creutzfeldt-Jakob Disease in Very Young People. (2021/10/26) ♡
• An in vivo Caenorhabditis elegans model for therapeutic research in human prion diseases. (2021/10/22) ♡
• 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. Sporadic Creutzfeldt-Jakob disease: Real-Time Quaking Induced Conversion (RT-QuIC) assay represents a major diagnostic advance. (2021/10/15) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. The First Sporadic Creutzfeldt-Jakob Disease Case with a Rare Molecular Subtype VV1 and 1-Octapeptide Repeat Deletion in PRNP. (2021/10/14) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. (18)FDG PET-CT in sporadic Creutzfeldt-Jakob disease, correlated with MRI and histology. (2021/10/12) ♡
• Neuronal excitatory-to-inhibitory balance is altered in cerebral organoid models of genetic neurological diseases. (2021/10/11) ♡
• Defining the Prion Type of Fatal Familial Insomnia. (2021/10/07) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Case Report: Extremely Early Detection of Preclinical Magnetic Resonance Imaging Abnormality in Creutzfeldt-Jakob Disease With the V180I Mutation. (2021/10/07) ♡
• Epidemiological and Clinical Characteristics of Sporadic Creutzfeldt-Jakob Disease: A Retrospective Study in Eastern China. (2021/10/06) ♡
• Loss of prion protein control of glucose metabolism promotes neurodegeneration in model of prion diseases. (2021/10/05) ♡
• Commentary or editorialiAn expert's opinion or commentary, not new research. Metastatic intracranial spread of adenocarcinoma mimicking Creutzfeldt-Jakob disease in two cases. (2021/10/01) ♡
• Potential for transmission of sporadic Creutzfeldt-Jakob disease through peripheral routes. (2021/10/01) ♡
• Phenotypic diversity of genetic Creutzfeldt-Jakob disease: a histo-molecular-based classification. (2021/10/01) ♡
• Neurology consultations in the intensive care units. (2021/10/01) ♡
• 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. Human Prion Disorders: Review of the Current Literature and a Twenty-Year Experience of the National Surveillance Center in the Czech Republic. (2021/10/01) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Bilateral hearing loss as an initial presentation of Creutzfeldt-Jakob disease. (2021/10/01) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. A rare case of Creutzfeldt-Jakob disease reported from Nepal. (2021/09/13) ♡
• Dementia in the Forensic Setting: Diagnoses Obtained Using a Condensed Protocol at the Office of Chief Medical Examiner, New York City. (2021/09/10) ♡
• Genetic prion disease-related mutation E196K displays a novel amyloid fibril structure revealed by cryo-EM. (2021/09/10) ♡
• Histotype-Dependent Oligodendroglial PrP Pathology in Sporadic CJD: A Frequent Feature of the M2C "Strain". (2021/09/09) ♡
• Characterization of Prion Disease Associated with a Two-Octapeptide Repeat Insertion. (2021/09/08) ♡
• Loss of PIKfyve drives the spongiform degeneration in prion diseases. (2021/09/07) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Variably Protease-sensitive Prionopathy in a Middle-aged Man With Rapidly Progressive Dementia. (2021/09/02) ♡
• Commentary or editorialiAn expert's opinion or commentary, not new research. Letter regarding the article entitled: 'Rapidly progressive sporadic Creutzfeldt-Jakob disease: isolated Heidenhain variant or a combination with PRES?'. (2021/09/01) ♡
• Commentary or editorialiAn expert's opinion or commentary, not new research. Reply to letter regarding the article entitled: 'Rapidly progressive sporadic Creutzfeldt-Jakob disease: isolated Heidenhain variant or a combination with PRES?'. (2021/09/01) ♡
• [Creutzfeldt-Jakob disease, experience in 17 patients]. (2021/09/01) ♡
• 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: Atypical Presentation of a Very Rare Disease]. (2021/08/31) ♡
• Prion strains associated with iatrogenic CJD in French and UK human growth hormone recipients. (2021/08/28) ♡
• 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. microRNA-146a-5p, Neurotropic Viral Infection and Prion Disease (PrD). (2021/08/25) ♡
• 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 with neuroleptic malignant syndrome. (2021/08/24) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Sporadic Creutzfeldt-Jakob Disease Appears to Be Sporadic Fatal Insomnia: A Case Report and Review of the Literature. (2021/08/23) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Hepatic Encephalopathy Mimicking Creutzfeldt-Jakob Disease on Laboratory, Physiological, and Imaging Evaluations. (2021/08/22) ♡
• Laboratory or animal researchiNo research in humans yet. Promising in a test tube or in mice unfortunately means nothing for patients. Propagation of CJD Prions in Primary Murine Glia Cells Expressing Human PrP(c). (2021/08/20) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Case Report: Paraneoplastic Hashimoto's Encephalopathy Associated With Lymphomatosis Cerebri With Periodic Synchronous Discharges Resembling Creutzfeldt-Jakob Disease. (2021/08/10) ♡
• Erratum to: Creutzfeldt-Jakob disease surveillance in Australia: update to 31 December 2020. (2021/08/09) ♡
• 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. Understanding Intra-Species and Inter-Species Prion Conversion and Zoonotic Potential Using Protein Misfolding Cyclic Amplification. (2021/08/03) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Diagnosis of Creutzfeldt-Jakob disease after neurosyphilis: just bad luck or misdiagnosed? (2021/08/01) ♡
• Cross-Linking Cellular Prion Protein Induces Neuronal Type 2-Like Hypersensitivity. (2021/07/30) ♡
• 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. Current Nosology of Neural Autoantibody-Associated Dementia. (2021/07/28) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Premortem diagnosis of pathologically confirmed sporadic Creutzfeldt-Jakob disease. (2021/07/23) ♡
• Creutzfeldt-Jakob disease surveillance in Australia: update to 31 December 2020. (2021/07/22) ♡
• Stern-Garcin Variant of Creutzfeldt-Jakob Disease. (2021/07/01) ♡
• 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 mimicking Lewy body dementia - a case report. (2021/06/30) ♡
• 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. MicroRNAs in Prion Diseases—From Molecular Mechanisms to Insights in Translational Medicine. (2021/06/29) ♡

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