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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)

• 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) ♡
• Frequent Detection of Pituitary-Derived PrPres in Human Prion Diseases. (2019/10/01) ♡
• National Variability in Prion Disease-Related Safety Policies for Neurologic Procedures. (2019/10/01) ♡
• α-Synuclein RT-QuIC assay in cerebrospinal fluid of patients with dementia with Lewy bodies. (2019/10/01) ♡
• Familial Creutzfeldt-Jakob Disease in an Indian Kindred. (2019/10/01) ♡
• 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 presenting with encephalopathy, rigidity, and hyperekplexia. (2019/10/01) ♡
• RNA editing alterations define manifestation of prion diseases. (2019/09/24) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Diagnostic challenge of rapidly progressing sporadic Creutzfeldt-Jakob disease. (2019/09/24) ♡
• Genetic Testing in Prion Disease: Psychological Consequences of the Decisions to Know or Not to Know. (2019/09/20) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. An autopsy case of MM2-thalamic subtype of sporadic Creutzfeldt-Jakob disease with Lewy bodies presenting as a sleep disorder mimicking anti-IgLON5 disease. (2019/09/15) ♡
• Laboratory or animal researchiNo research in humans yet. Promising in a test tube or in mice unfortunately means nothing for patients. Prion disease is accelerated in mice lacking stress-induced heat shock protein 70 (HSP70). (2019/09/13) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Real-time Quaking-induced Conversion Assay for the Diagnosis of Sporadic Creutzfeldt-Jakob Disease in a Living Patient. (2019/09/09) ♡
• Importance of Neuropathological Diagnosis of Dementia Patients in Family Practice. (2019/09/04) ♡
• Profiles of 14-3-3 and Total Tau in CSF Samples of Chinese Patients of Different Genetic Prion Diseases. (2019/09/04) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Creutzfeldt-Jakob Disease Presenting with Abducens Nerve Palsy. (2019/09/04) ♡
• The Predictive Value of Endpoint Quaking-Induced Conversion in Creutzfeldt-Jakob Disease. (2019/09/01) ♡
• 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. Amplification techniques and diagnosis of prion diseases. (2019/09/01) ♡
• Commentary or editorialiAn expert's opinion or commentary, not new research. Atypical clinical presentation of variant Creutzfeldt-Jakob disease. (2019/09/01) ♡
• [Prion induced spongiform encephalopathy of Creutzfeldt-Jakob disease]. (2019/09/01) ♡
• Familial Creutzfeldt-Jakob Disease with a PRNP Mutation at Codon 180 Presented with Visual Hallucinations and Illusions. (2019/09/01) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. THK5351 and flortaucipir PET with pathological correlation in a Creutzfeldt-Jakob disease patient: a case report. (2019/08/29) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. The Evolution of Movement Disorders in N-Methyl-D-Aspartate Receptor Encephalitis-A Video Log. (2019/08/16) ♡
• Creutzfeldt-Jakob disease surveillance in Australia: update to 31 December 2018. (2019/08/15) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Novel prion mutation (p.Tyr225Cys) in a Korean patient with atypical Creutzfeldt-Jakob disease. (2019/08/02) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. First European case of Creutzfeldt-Jakob disease with a PRNP G114V mutation. (2019/08/01) ♡
• 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. Insights into the Bidirectional Properties of the Sheep-Deer Prion Transmission Barrier. (2019/08/01) ♡
• 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. Learning from history: Lord Brain and Hashimoto's encephalopathy. (2019/08/01) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Public health concerns regarding sporadic Creutzfeldt-Jakob disease in China: a case series. (2019/08/01) ♡
• Production of seedable Amyloid-β peptides in model of prion diseases upon PrP(Sc)-induced PDK1 overactivation. (2019/08/01) ♡
• 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. (2019/08/01) ♡
• 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. Mutations in Prion Protein Gene: Pathogenic Mechanisms in C-Terminal vs. N-Terminal Domain, a Review. (2019/07/23) ♡
• Creutzfeldt–Jakob disease surveillance in Australia: update to December 2017. (2019/07/16) ♡
• Laboratory or animal researchiNo research in humans yet. Promising in a test tube or in mice unfortunately means nothing for patients. Biological Assessment of a (18)F-Labeled Sulforhodamine 101 in a Mouse Model of Alzheimer's Disease as a Potential Astrocytosis Marker. (2019/07/16) ♡
• Early-onset Alzheimer's disease patient with prion (PRNP) p.Val180Ile mutation. (2019/07/16) ♡
• Plasma YKL-40 in the spectrum of neurodegenerative dementia. (2019/07/12) ♡
• Analysis of RNA Expression Profiles Identifies Dysregulated Vesicle Trafficking Pathways in Creutzfeldt-Jakob Disease. (2019/07/01) ♡
• Detection of Cell-Free Mitochondrial DNA in Cerebrospinal Fluid of Creutzfeldt-Jakob Patients. (2019/06/21) ♡
• Epitope mapping of the protease resistant products of RT-QuIC does not allow the discrimination of sCJD subtypes. (2019/06/17) ♡
• 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. Review: Fluid biomarkers in the human prion diseases. (2019/06/01) ♡
• Tracking and clarifying differential traits of classical- and atypical L-type bovine spongiform encephalopathy prions after transmission from cattle to cynomolgus monkeys. (2019/05/16) ♡

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