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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)

• 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) ♡
• Prion Seeds Distribute throughout the Eyes of Sporadic Creutzfeldt-Jakob Disease Patients. (2018/11/20) ♡
• Review of diffuse cortical injury on diffusion-weighted imaging in acutely encephalopathic patients with an acronym: "CRUMPLED". (2018/11/09) ♡
• 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 Nonconvulsive Status Epilepticus. (2018/11/04) ♡
• 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 Diseases. (2018/11/01) ♡
• 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. Unravelling the glial response in the pathogenesis of Alzheimer's disease. (2018/11/01) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Lenalidomide induced reversible parkinsonism, dystonia, and dementia in subclinical Creutzfeldt-Jakob disease. (2018/10/15) ♡
• Overexpression of quality control proteins reduces prion conversion in prion-infected cells. (2018/10/12) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Clinical Reasoning: Rapidly progressive dementia in a patient with HIV after an exotic journey. (2018/10/02) ♡
• 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. Oligodendrogliopathy in neurodegenerative diseases with abnormal protein aggregates: The forgotten partner. (2018/10/01) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Autopsied case of non-plaque-type dura mater graft-associated Creutzfeldt-Jakob disease presenting with extensive amyloid-β deposition. (2018/10/01) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Sporadic Creutzfeldt-Jakob disease with glial PrP(Res) nuclear and perinuclear immunoreactivity. (2018/10/01) ♡
• 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. Diagnostic challenges in rapidly progressive dementia. (2018/10/01) ♡
• Rapidly Progressive Dementia in the Outpatient Clinic: More Than Prions. (2018/10/01) ♡
• Analysis of 22 Years of Surveillance for Prion Diseases in Slovenia, 1996 to 2017. (2018/10/01) ♡
• 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 with unusual presentation of peripheral neuropathy and ophthalmoplegia. (2018/10/01) ♡
• Effect of Urea, Arginine, and Ethanol Concentration on Aggregation of (179)CVNITV(184) Fragment of Sheep Prion Protein. (2018/09/30) ♡
• 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 Evaluation of Rapidly Progressive Dementia Culminating in a Diagnosis of Creutzfeldt-Jakob Disease. (2018/09/23) ♡
• A Bioluminescent Cell Assay to Quantify Prion Protein Dimerization. (2018/09/21) ♡
• Muskelin Coordinates PrP(C) Lysosome versus Exosome Targeting and Impacts Prion Disease Progression. (2018/09/19) ♡
• 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 Progressing Sporadic Creutzfeldt-Jakob Disease Presenting as a Stroke. (2018/09/13) ♡
• 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 MM-1 Type Creutzfeldt-Jakob Disease With Hemiballic Presentation and No Cognitive Impairment Until Death: How New NCJDRSU Diagnostic Criteria May Allow Early Diagnosis. (2018/09/05) ♡
• Sporadic Fatal Insomnia in Europe: Phenotypic Features and Diagnostic Challenges. (2018/09/01) ♡
• Chorea in Sporadic Creutzfeldt-Jakob Disease. (2018/09/01) ♡
• 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. A systematic review comparing the diagnostic value of 14-3-3 protein in the cerebrospinal fluid, RT-QuIC and RT-QuIC on nasal brushing in sporadic Creutzfeldt-Jakob disease. (2018/09/01) ♡
• Extending the functional characteristics of naturally occurring autoantibodies against β-amyloid, prion protein and α-synuclein. (2018/08/29) ♡
• 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 Predisposition to Infectious Disease. (2018/08/27) ♡
• Susceptibility to Creutzfeldt-Jakob disease after human growth hormone treatment in France. (2018/08/21) ♡
• Unexpected prion phenotypes in experimentally transfused animals: predictive models for humans? (2018/08/16) ♡
• 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. Characterization of mutations in PRNP (prion) gene and their possible roles in neurodegenerative diseases. (2018/08/14) ♡
• Commentary or editorialiAn expert's opinion or commentary, not new research. PrP(res) deposition in the retina is a common finding of sporadic, familial and iatrogenic Creutzfeldt-Jakob diseases (CJD). (2018/08/10) ♡
• Post-mortem magnetic resonance imaging in patients with suspected prion disease: Pathological confirmation, sensitivity, specificity and observer reliability. A national registry. (2018/08/07) ♡
• Impaired transmissibility of atypical prions from genetic CJD(G114V). (2018/08/07) ♡
• RFAmyloid: A Web Server for Predicting Amyloid Proteins. (2018/07/16) ♡
• Interlaboratory validation of cerebrospinal fluid α-synuclein quantification in the diagnosis of sporadic Creutzfeldt-Jakob disease. (2018/07/07) ♡
• Predictive Factors for Early Initiation of Artificial Feeding in Patients With Sporadic Creutzfeldt-Jakob Disease. (2018/07/03) ♡
• 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 critical review of the prion hypothesis of human synucleinopathies. (2018/07/01) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Primary Central Nervous System Lymphoma with Associated Demyelination and Creutzfeldt Astrocytes. (2018/07/01) ♡
• CSF nonphosphorylated Tau as a biomarker for the discrimination of AD from CJD. (2018/05/26) ♡
• 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. Intravascular large B-cell lymphoma presenting clinically as rapidly progressive dementia. (2018/05/01) ♡

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