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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 (1007)

• Person and ethics of a psychiatrist during National Socialism: Friedrich Meggendorfer (1880-1953). (2020/03/01) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Hallucinatory palinopsia and paroxysmal oscillopsia as initial manifestations of sporadic Creutzfeldt-Jakob disease: A case study. (2020/03/01) ♡
• 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. Metal homeostasis disturbances in neurodegenerative disorders, with special emphasis on Creutzfeldt-Jakob disease - Potential pathogenetic mechanism and therapeutic implications. (2020/03/01) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Genetic Creutzfeldt-Jakob disease mimicking dementia with Lewy bodies: Clinical and radiological findings. (2020/02/15) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. A case of M232R genetic Creutzfeldt-Jakob disease with Lewy bodies. (2020/02/15) ♡
• Neutralizing Mutations Significantly Inhibit Amyloid Formation by Human Prion Protein and Decrease Its Cytotoxicity. (2020/02/14) ♡
• 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. Neuropathology of Lewy body disease: Clinicopathological crosstalk between typical and atypical cases. (2020/02/01) ♡
• Cerebrospinal fluid non-phosphorylated tau in the differential diagnosis of Creutzfeldt-Jakob disease: a comparative prospective study with 14-3-3. (2020/02/01) ♡
• Self-assembly hollow manganese Prussian white nanocapsules attenuate Tau-related neuropathology and cognitive decline. (2020/02/01) ♡
• Correlating diffusion-weighted MRI intensity with type 2 pathology in mixed MM-type sporadic Creutzfeldt-Jakob disease. (2020/01/15) ♡
• A pilot study of the utility of cerebrospinal fluid neurofilament light chain in differentiating neurodegenerative from psychiatric disorders: A 'C-reactive protein' for psychiatrists and neurologists? (2020/01/01) ♡
• 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. Prion disease and recommended procedures for flexible endoscope reprocessing - a review of policies worldwide and proposal for a simplified approach. (2020/01/01) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Prion Problem: A Rapidly Progressive Dementia. (2020/01/01) ♡
• Inactivation Methods for Prions. (2020/01/01) ♡
• 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. Introduction to Current Progress in Advanced Research on Prions. (2020/01/01) ♡
• Spatial Epidemiology of Sporadic Creutzfeldt-Jakob Disease in Apulia, Italy. (2020/01/01) ♡
• Metabolic Changes Detected by 18F-FDG PET in the Preclinical Stage of Familial Creutzfeldt-Jakob Disease. (2020/01/01) ♡
• 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. Strain variation in treatment and prevention of human prion diseases. (2020/01/01) ♡
• 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 utility of bank voles for studying prion disease. (2020/01/01) ♡
• 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 Review of Neuroimaging in Rare Neurodegenerative Diseases. (2020/01/01) ♡
• Clinical trialiResearch in patients, without randomization between groups. Useful, but less certain than a randomized trial. CSF biomarkers of neuroinflammation in distinct forms and subtypes of neurodegenerative dementia. (2019/12/31) ♡
• Identification of circulating microRNA signatures as potential biomarkers in the serum of elk infected with chronic wasting disease. (2019/12/23) ♡
• Postmortem Quantitative Analysis of Prion Seeding Activity in the Digestive System. (2019/12/16) ♡
• Quaking-induced conversion of prion protein on a thermal mixer accelerates detection in brains infected with transmissible spongiform encephalopathy agents. (2019/12/12) ♡
• 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. Movement Disorders in Prionopathies: A Systematic Review. (2019/12/12) ♡
• 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 reported case of Creutzfeldt-Jakob disease from Nepal. (2019/12/12) ♡
• Two distinct prions in fatal familial insomnia and its sporadic form. (2019/12/09) ♡
• 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. Genetic Factors in Mammalian Prion Diseases. (2019/12/03) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Creutzfeldt-Jakob Disease Mimicking Neurosyphilis: A Complex Presentation, Histopathological Findings, and Special Precautions for Autopsy. (2019/12/01) ♡
• Impact of pyridine-2-carboxaldehyde-derived aroylhydrazones on the copper-catalyzed oxidation of the M112A PrP(103-112) mutant fragment. (2019/12/01) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Autopsy case of MV2K-type sporadic Creutzfeldt-Jakob disease with spongiform changes of the cerebral cortex. (2019/12/01) ♡
• Diagnostic value of surrogate CSF biomarkers for Creutzfeldt-Jakob disease in the era of RT-QuIC. (2019/12/01) ♡
• Domain-specific Quantification of Prion Protein in Cerebrospinal Fluid by Targeted Mass Spectrometry. (2019/12/01) ♡
• A Case of Creutzfeldt-Jakob Disease Presented as Rapid Progressive Parkinsonism. (2019/12/01) ♡
• Evaluation of Human Cerebrospinal Fluid Malate Dehydrogenase 1 as a Marker in Genetic Prion Disease Patients. (2019/11/28) ♡
• Million-fold sensitivity enhancement in proteopathic seed amplification assays for biospecimens by Hofmeister ion comparisons. (2019/11/12) ♡
• Role of prion protein glycosylation in replication of human prions by protein misfolding cyclic amplification. (2019/11/01) ♡
• The association of quantitative EEG and MRI in Creutzfeldt-Jakob Disease. (2019/11/01) ♡
• Clinical Variability in P102L Gerstmann-Sträussler-Scheinker Syndrome. (2019/11/01) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Cortical Ribbon Sign in Acute Hepatic Encephalopathy with Sequential Atrophy. (2019/11/01) ♡
• 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. The cellular prion protein and its derived fragments in human prion diseases and their role as potential biomarkers. (2019/11/01) ♡
• Molecular Characterization of the Danish Prion Diseases Cohort With Special Emphasis on Rare and Unique Cases. (2019/11/01) ♡
• 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. Diagnostics of sporadic Creutzfeldt-Jakob disease – literature review. (2019/10/31) ♡
• Transgenic mouse models expressing human and macaque prion protein exhibit similar prion susceptibility on a strain-dependent manner. (2019/10/30) ♡
• Clinical trialiResearch in patients, without randomization between groups. Useful, but less certain than a randomized trial. Study protocol for enhanced CJD surveillance in the 65+ years population group in Scotland: an observational neuropathological screening study of banked brain tissue donations for evidence of prion disease. (2019/10/28) ♡
• Scrapie susceptibility-associated indel polymorphism of shadow of prion protein gene (SPRN) in Korean native black goats. (2019/10/24) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Three Cases of Creutzfeldt-Jakob Disease with Visual Disturbances as Initial Manifestation. (2019/10/23) ♡
• 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 32-2019: A 70-Year-Old Woman with Rapidly Progressive Ataxia. (2019/10/17) ♡
• Inactivation of chronic wasting disease prions using sodium hypochlorite. (2019/10/04) ♡
• Prokaryotic SPHINX replication sequences are conserved in mammalian brain and participate in neurodegeneration. (2019/10/01) ♡

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