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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)

• Laboratory or animal researchiNo research in humans yet. Promising in a test tube or in mice unfortunately means nothing for patients. Stimulations of the Culture Medium of Activated Microglia and TNF-Alpha on a Scrapie-Infected Cell Line Decrease the Cell Viability and Induce Marked Necroptosis That Also Occurs in the Brains from the Patients of Human Prion Diseases. (2019/03/20) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Cortical Hyperintensity on Diffusion-weighted Images as the Presymptomatic Marker of Sporadic Creutzfeldt-Jakob Disease. (2019/03/01) ♡
• 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. Renewed assessment of the risk of emergent advanced cell therapies to transmit neuroproteinopathies. (2019/03/01) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. [MRI role in Creutzfeldt-Jakob disease: about a case]. (2019/02/28) ♡
• RT-QuIC: a new test for sporadic CJD. (2019/02/01) ♡
• Cerebrospinal fluid neurofilament light in suspected sporadic Creutzfeldt-Jakob disease. (2019/02/01) ♡
• Neurofilament light chain in serum for the diagnosis of amyotrophic lateral sclerosis. (2019/02/01) ♡
• 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. Diagnostic biomarkers for Parkinson's disease: focus on α-synuclein in cerebrospinal fluid. (2019/02/01) ♡
• 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 atypical outcome of sporadic Creutzfeldt-Jakob disease in an elderly patient]. (2019/01/01) ♡
• Commentary or editorialiAn expert's opinion or commentary, not new research. Instrument cleanliness and protein misfolding disorders. (2019/01/01) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Sporadic CJD in association with HIV. (2019/01/01) ♡
• A network analysis based approach to characterizing periodic sharp wave complexes in electroencephalograms of patients with sporadic CJD. (2019/01/01) ♡
• Aluminum in neurological disease - a 36 year multicenter study. (2019/01/01) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. An autopsied case of MM1-type sporadic Creutzfeldt-Jakob disease with pathology of Wernicke encephalopathy. (2019/01/01) ♡
• 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. Proteasome: a Nanomachinery of Creative Destruction. (2019/01/01) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Clinicopathological findings of an MM2-cortical-type sporadic Creutzfeldt-Jakob disease patient with cortical blindness during a course of glaucoma and age-related macular degeneration. (2019/01/01) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Rare genetic Creutzfeldt-Jakob disease with E196A mutation: a case report. (2019/01/01) ♡
• 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. [Protective Role of the Host Innate Immune System in Prion Pathogenesis]. (2019/01/01) ♡
• Sensitivity and specificity evaluation of multiple neurodegenerative proteins for Creutzfeldt-Jakob disease diagnosis using a deep-learning approach. (2019/01/01) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. A case of V180I genetic Creutzfeldt-Jakob disease presenting with conspicuous facial mimicry. (2019/01/01) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. The worst is yet to come: probable sporadic Creutzfeldt-Jakob disease in a well-controlled HIV patient. (2019/01/01) ♡
• 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. Therapies for prion diseases. (2019/01/01) ♡
• Prion disease diagnosis using subject-specific imaging biomarkers within a multi-kernel Gaussian process. (2019/01/01) ♡
• Meta-analysisiAll studies on one question combined and calculated together. This is the strongest form of research that exists: a single loose study can be coincidence, dozens together much less so. The label says something about the design, not about the outcome — which can also be that something does NOT work. Neurofilament Light Chain in Cerebrospinal Fluid and Blood as a Biomarker for Neurodegenerative Diseases: A Systematic Review and Meta-Analysis. (2019/01/01) ♡
• Significant enhanced expressions of aquaporin-1, -4 and -9 in the brains of various prion diseases. (2019/01/01) ♡
• [Rapidly progressive dementia]. (2019/01/01) ♡
• Recombinant prion protein vaccination of transgenic elk PrP mice and reindeer overcomes self-tolerance and protects mice against chronic wasting disease. (2018/12/21) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Co-occurrence of chronic traumatic encephalopathy and prion disease. (2018/12/18) ♡
• Sample Pooling and Inflammation Linked to the False Selection of Biomarkers for Neurodegenerative Diseases in Top-Down Proteomics: A Pilot Study. (2018/12/18) ♡
• Commentary or editorialiAn expert's opinion or commentary, not new research. Crossed cerebellar diaschisis in Creutzfeldt-Jakob disease evaluated through single photon emission computed tomography. (2018/12/15) ♡
• Antemortem CSF Aβ42/Aβ40 ratio predicts Alzheimer's disease pathology better than Aβ42 in rapidly progressive dementias. (2018/12/14) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Imaging Manifestations of Creutzfeldt-Jakob Disease and Case Series. (2018/12/13) ♡
• 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. Arm Levitation as Initial Manifestation of Creutzfeldt-Jakob Disease: Case Report and Review of the Literature. (2018/12/10) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Drug-induced Creutzfeldt-Jakob disease-like syndrome: early CSF analysis as useful tool for differential diagnosis. (2018/12/04) ♡
• 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 Heidenhain variant of Creutzfeldt-Jakob disease. (2018/12/02) ♡
• Age at onset of genetic (E200K) and sporadic Creutzfeldt-Jakob diseases is modulated by the CYP4X1 gene. (2018/12/01) ♡
• Modeling amyloid beta and tau pathology in human cerebral organoids. (2018/12/01) ♡
• 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 V180I genetic Creutzfeldt-Jakob disease presenting with early disease pathology. (2018/12/01) ♡
• Evaluation of the effect of various main elements on the PrPSc detection by real-time quaking-induced conversion assay. (2018/12/01) ♡
• Distinct microglia profile in Creutzfeldt-Jakob disease and Alzheimer's disease is independent of disease kinetics. (2018/12/01) ♡
• Commentary or editorialiAn expert's opinion or commentary, not new research. Longitudinal brain magnetic resonance imaging and real-time quaking induced conversion analysis in presymptomatic Creutzfeldt-Jakob disease. (2018/12/01) ♡
• The Brain Donation Program in South Korea. (2018/12/01) ♡
• Transmission of amyloid-β protein pathology from cadaveric pituitary growth hormone. (2018/12/01) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Clinics in diagnostic imaging (193). Sporadic Creutzfeldt-Jakob disease (sCJD). (2018/12/01) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. A case of probable sporadic Creutzfeldt-Jakob disease in a tertiary care hospital in Malaysia. (2018/12/01) ♡
• Creutzfeldt-Jakob disease surveillance in Eastern Slovakia from 2004 to 2016. (2018/12/01) ♡
• Prion pathogenesis is unaltered in a mouse strain with a permeable blood-brain barrier. (2018/11/29) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. [A case of Creutzfeldt-Jakob disease with E200K mutation presenting with hearing loss and central hypoventilation]. (2018/11/28) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. [Genetic Creutzfeldt-Jakob disease with a glutamate-to-lysine substitution at codon 219 (E219K) in the presence of the E200K mutation presenting with rapid progressive dementia following slowly progressive clinical course]. (2018/11/28) ♡
• Nonpathogenic Heterologous Prions Can Interfere with Prion Infection in a Strain-Dependent Manner. (2018/11/27) ♡

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