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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)

• Commentary or editorialiAn expert's opinion or commentary, not new research. Effect of SARS-CoV-2 Incidence and Immunisation Rates on Sporadic Creutzfeldt-Jakob Disease Incidence. (2024/01/01) ♡
• 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 Importance of Long-term Partner Observation in Cognitive Evaluation: A Very Early Creutzfeldt-Jakob Disease in a Patient with Mild Cognitive Impairment. (2024/01/01) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Creutzfeldt-Jakob disease: clinical cases. (2024/01/01) ♡
• 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. [Difficulties in lifetime diagnosis of Creutzfeldt-Jakob disease]. (2024/01/01) ♡
• Anti-DPPX encephalitis mimicking Creutzfeldt-Jakob Disease: first case report in Poland. (2024/01/01) ♡
• 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 Devastating Neurological Disorder: Anti-Dipeptidyl-Peptidase-Like Protein 6 (DPPX) Encephalitis Causing Rapidly Progressive Dementia. (2023/12/26) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Probable Sporadic Creutzfeldt-Jakob Disease Presenting as Refractory Status Epilepticus in a Poststroke Epilepsy Patient: A Case Report. (2023/12/20) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Primary progressive aphasia with focal periodic sharp wave complexes: An unusual manifestation of Creutzfeldt-Jakob disease. (2023/12/18) ♡
• 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: Brain MRI lesion features from 2 cases reports. (2023/12/17) ♡
• [Review of a series of cases of Creutzfeldt-Jakob disease in a tertiary care hospital]. (2023/12/16) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Systematic approach to diagnosing suspected Creutzfeldt-Jakob disease. (2023/12/07) ♡
• Neural cell engraftment therapy for sporadic Creutzfeldt-Jakob disease restores neuroelectrophysiological parameters in a cerebral organoid model. (2023/12/05) ♡
• A Study of Clinical Profile, Radiological and Electroencephalographic Characteristics of Sporadic Creutzfeldt-Jakob Disease From a Tertiary Care Hospital. (2023/12/05) ♡
• PRNP gene polymorphism frequencies for comparing possible vulnerability to BSE in Chinese bovine population. (2023/12/01) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. V180I genetic Creutzfeldt-Jakob disease: Severe degeneration of the inferior olivary nucleus in an autopsied patient with identification of the M2T prion strain. (2023/12/01) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. An autopsy case of variably protease-sensitive prionopathy with Met/Met homogeneity at codon 129. (2023/12/01) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Anti-recoverin antibody positive Heidenhain variant CJD: a case report. (2023/12/01) ♡
• The role of neuronal antibodies in cryptogenic new onset refractory status epilepticus. (2023/12/01) ♡
• Gut microbiota and metabolome in sporadic Creutzfeldt-Jakob disease. (2023/12/01) ♡
• Detection of prions in the urine of patients affected by sporadic Creutzfeldt-Jakob disease. (2023/12/01) ♡
• 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 role of cellular prion protein in immune system. (2023/12/01) ♡
• Diagnostic accuracy of diffusion-weighted imaging in variant Creutzfeldt-Jakob disease. (2023/12/01) ♡
• Two Chinese patients of sporadic Creutzfeldt-Jakob disease with a S97N mutation in PRNP gene. (2023/12/01) ♡
• Prospective 25-year surveillance of prion diseases in France, 1992 to 2016: a slow waning of epidemics and an increase in observed sporadic forms. (2023/12/01) ♡
• CSF 14-3-3β is associated with progressive cognitive decline in Alzheimer's disease. (2023/11/22) ♡
• Validation of the Medical Research Council prion disease rating scale in France. (2023/11/08) ♡
• Short incubation periods of atypical H-type BSE in cattle with EK211 and KK211 prion protein genotypes after intracranial inoculation. (2023/11/03) ♡
• Development of a sensitive real-time quaking-induced conversion (RT-QuIC) assay for application in prion-infected blood. (2023/11/02) ♡
• Utility of Repeat Endpoint Quaking-Induced Conversion Testing in Creutzfeldt-Jakob Disease. (2023/11/01) ♡
• Laboratory or animal researchiNo research in humans yet. Promising in a test tube or in mice unfortunately means nothing for patients. Conservation of vCJD Strain Properties After Extraction and In Vitro Propagation of PrP(Sc) from Archived Formalin-Fixed Brain and Appendix Tissues Using Highly Sensitive Protein Misfolding Cyclic Amplification. (2023/11/01) ♡
• Spontaneous prion disease in homozygous and heterozygous transgenic mouse models of T188K genetic Creutzfeldt-Jakob disease. (2023/11/01) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Rapid progression of probable Creutzfeldt-Jakob disease with concomitant COVID-19 infection. (2023/11/01) ♡
• Geographic Diversity in the Incidence of Human Prion Diseases - China, 2006-2019. (2023/10/27) ♡
• 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: A Rare Case of Dementia. (2023/10/17) ♡
• 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 Progressive Dementia in an Elderly Male: Perseverance Becomes the Key to a Rare Diagnosis. (2023/10/17) ♡
• 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. Human prion diseases and the prion protein - what is the current state of knowledge? (2023/10/16) ♡
• Magnetic resonance imaging arterial spin labeling hypoperfusion with diffusion-weighted image hyperintensity is useful for diagnostic imaging of Creutzfeldt-Jakob disease. (2023/10/10) ♡
• 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. Potential Therapeutic Use of Stem Cells for Prion Diseases. (2023/10/07) ♡
• 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 Creutzfeldt-Jakob disease in a patient with multimorbidity: a case-report. (2023/10/02) ♡
• Elevated E200K Somatic Mutation of the Prion Protein Gene (PRNP) in the Brain Tissues of Patients with Sporadic Creutzfeldt-Jakob Disease (CJD). (2023/10/02) ♡
• High diagnostic performance of plasma and cerebrospinal fluid beta-synuclein for sporadic Creutzfeldt-Jakob disease. (2023/10/01) ♡
• Removal of UK-donor deferral for variant Creutzfeldt-Jakob disease: A large donation gain in Australia. (2023/10/01) ♡
• 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 Slow Progression:Report of One Case]. (2023/10/01) ♡
• Anti-prion drugs do not improve survival in knock-in models of inherited prion disease. (2023/09/29) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Sporadic Creutzfeldt-Jakob Disease With COVID-19 Infection: A Case Report. (2023/09/22) ♡
• Diagnostic and prognostic value of cerebrospinal fluid SNAP-25 and neurogranin in Creutzfeldt-Jakob disease in a clinical setting cohort of rapidly progressive dementias. (2023/09/08) ♡
• Understanding the key features of the spontaneous formation of bona fide prions through a novel methodology that enables their swift and consistent generation. (2023/09/07) ♡
• 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 Korsakoff syndrome caused by E196A mutation in PRNP gene: A case report. (2023/09/06) ♡
• The epidemiological and clinical characteristics of patients with young-onset genetic Creutzfeldt-Jakob disease. (2023/09/01) ♡
• Risk of variant Creutzfeldt-Jakob disease in a simulated cohort of Canadian blood donors. (2023/09/01) ♡

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