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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)

• 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) ♡
• 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 Case of Anti-LGI1 Limbic Encephalitis with New Onset Epilepsy: A Case Report. (2019/05/07) ♡
• Cerebrospinal Fluid Total and Phosphorylated α-Synuclein in Patients with Creutzfeldt-Jakob Disease and Synucleinopathy. (2019/05/01) ♡
• 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 new neurobehavioral phenotype of familial Creutzfeldt-Jakob disease: impaired theory of mind. (2019/05/01) ♡
• Disease duration in E200K familial Creutzfeldt-Jakob disease is correlated with clinical, radiological, and laboratory variables. (2019/05/01) ♡
• The Heidenhain variant of Creutzfeldt-Jakob disease. (2019/05/01) ♡
• Cerebrospinal Fluid Total Prion Protein in the Spectrum of Prion Diseases. (2019/04/01) ♡
• Prokaryotic SPHINX 1.8 REP protein is tissue-specific and expressed in human germline cells. (2019/04/01) ♡
• Surveillance for variant CJD: should more children with neurodegenerative diseases have autopsies? (2019/04/01) ♡
• Prion-related peripheral neuropathy in sporadic Creutzfeldt-Jakob disease. (2019/04/01) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Psychosis as debut of sporadic Creutzfeldt-Jakob disease. (2019/04/01) ♡
• Distinctive FDG-PET/CT Findings in Acute Neurological Hospital Care. (2019/04/01) ♡

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