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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)

• 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-When Proteins Turn Lethal: Creutzfeldt-Jakob Disease (CJD) and the Quest for Classification, Diagnosis, Therapeutic Approaches, and Emerging Research. (2026/04/11) ♡
• Commentary or editorialiAn expert's opinion or commentary, not new research. A wolf in synuclein clothing: Creutzfeldt-Jakob disease disguised as MSA. (2026/04/01) ♡
• Clinical trialiResearch in patients, without randomization between groups. Useful, but less certain than a randomized trial. The Phenotypic Spectrum of Sporadic Creutzfeldt-Jakob Disease Cortical Subtype. (2026/04/01) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Variably Protease-Sensitive Prionopathy: Two New Cases With Motor Neuron-Dementia Syndrome. (2026/04/01) ♡
• 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. Antibodies in Creutzfeldt-Jakob disease: A systematic review of patient characteristics, diagnostics, and clinical implications. (2026/04/01) ♡
• 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 diseases : Creutzfeldt-Jakob and differential diagnoses]. (2026/04/01) ♡
• Cross-disease genetic and epigenetic architecture of the MOBP locus shows convergence in ALS-PSP. (2026/03/27) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. When Thiamine Is Not the Answer: Sporadic Creutzfeldt-Jakob Disease Mimicking Wernicke's Encephalopathy. (2026/03/16) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Diagnosis of Sporadic Creutzfeldt-Jakob Disease in Both Kidney Recipients From the Same Donor: Was It Graft Transmission? (2026/03/14) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Late-Onset Depression Mimicking a Primary Psychiatric Disorder: Diagnostic Pitfalls in Sporadic Creutzfeldt-Jakob Disease. (2026/03/14) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Creutzfeldt-Jakob Disease: Spectrum of Symptoms, Clinical Progress and Diagnostics-Report of Five Cases. (2026/03/10) ♡
• Prevalence and clinical effects of Lewy Body pathology in non-prion rapidly progressive dementias: a retrospective cohort study. (2026/03/06) ♡
• Prognostic Value of CSF Total Tau Protein in Patients with Familial and Sporadic Creutzfeldt-Jakob Disease. (2026/03/05) ♡
• Tri-Band Rhythmicity on Quantitative EEG: A Clinically Applicable Marker for Sporadic Creutzfeldt-Jakob Disease. (2026/03/03) ♡
• Variant Creutzfeldt-Jakob disease surveillance in Spain, 1993-2021. (2026/03/03) ♡
• Creutzfeldt-Jakob Disease with Abnormality of Periaqueductal Gray Matter Region at Diffusion-Weighted Magnetic Resonance Imaging. (2026/03/01) ♡
• Epidemiology of progressive intellectual and neurological deterioration in UK children. (2026/03/01) ♡
• Commentary or editorialiAn expert's opinion or commentary, not new research. Transmission Ratio Distortion in Genetic Prion Diseases: Clarifying Methodological Considerations. (2026/03/01) ♡
• Commentary or editorialiAn expert's opinion or commentary, not new research. Letter to the Editor Regarding Kortazar-Zubizarreta et al. 'The Risk of Transmission of Genetic Prion Diseases Is Greater Than 50%'. (2026/03/01) ♡
• Laboratory or animal researchiNo research in humans yet. Promising in a test tube or in mice unfortunately means nothing for patients. Limited transmission of V180I genetic Creutzfeldt-Jakob disease in knock-in mice models. (2026/03/01) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Unusual occurrence of temporo-spatial cluster of human prion disease in northern part of central Slovakia. (2026/03/01) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. [Rapidly progressive neurocognitive symptoms - consider rare aetiologies]. (2026/03/01) ♡
• Strain Traits of Intracranially Administered L-Type Bovine Spongiform Encephalopathy Prions Are not Significantly Modified During Intraspecies Transmission in Cynomolgus Monkeys. (2026/03/01) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Sporadic Creutzfeldt-Jakob Disease With Spinal Cord Lesions: A Case Report. (2026/02/19) ♡
• Distinct neuronal alterations distinguish two subtypes of sporadic Creutzfeldt-Jakob disease with shared dysfunctional pathways. (2026/02/12) ♡
• Alterations in cerebrospinal fluid levels of myelin- and oligodendrocyte-related proteins in sporadic Creutzfeldt-Jakob disease. (2026/02/10) ♡
• State of the art in biosafety at the European National Reference Laboratories for Transmissible Spongiform Encephalopathies. (2026/02/10) ♡
• D178N prion protein mutation endows RML prions with new strain properties that do not mimic human genetic prion diseases. (2026/02/10) ♡
• High Proportions of GAP43 Positivity in the Cerebrospinal Fluids of Patients with Sporadic and Certain Types of Genetic Creutzfeldt-Jakob Diseases by Western Blot Analysis. (2026/02/09) ♡
• 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 Disease: Pathogenesis, Diagnosis and Public Health. (2026/02/06) ♡
• 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 in Palestine with early ataxia and dysarthria: a case report. (2026/02/02) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Co-occurrence of lung adenocarcinoma with rapidly progressive dementia and multiple cerebral microbleeds: a case report. (2026/02/02) ♡
• 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. New Frontiers in Animal Prion Diseases. (2026/02/01) ♡
• Commentary or editorialiAn expert's opinion or commentary, not new research. PRES-like MRI findings in sporadic Creutzfeldt-Jakob disease: a case report. (2026/02/01) ♡
• 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. Genetic causes and modifiers of prion diseases. (2026/02/01) ♡
• A critical perspective of prion disease surveillance in Brazil. (2026/01/29) ♡
• 18F-DPA-714 PET/MRI reveals early and widespread neuroinflammation in sporadic Creutzfeldt-Jakob disease: a case report. (2026/01/28) ♡
• Advancing prion diagnostics: full-length human E200K RT-QuIC substrate facilitates prion detection in tear fluid and improves sensitivity in cerebrospinal fluid. (2026/01/22) ♡
• 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 as a key for early diagnosis of Creutzfeldt-Jakob disease]. (2026/01/19) ♡
• 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 Encephalopathy in a 49-Year-Old Female: Creutzfeldt-Jakob Disease. (2026/01/16) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. A Unique Case of Genetic Creutzfeldt-Jakob Disease (E200K Mutation) with CSF-restricted Anti Myelin Oligodendrocyte Glycoprotein Antibody. (2026/01/15) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Unexplained Acute Homonymous Hemianopia as a Presentation of Creutzfeldt-Jakob Disease. (2026/01/14) ♡
• Genetic Creutzfeldt-Jakob disease linked to the E200K mutation: a large cohort study. (2026/01/13) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. Rapidly progressive sensorineural hearing loss due to sporadic Creutzfeldt-Jakob disease. (2026/01/12) ♡
• Encephalopathic EEG Patterns. (2026/01/10) ♡
• Alpha-synuclein seeding activity in postmortem tissues from patients with diffuse and isolated Lewy bodies. (2026/01/07) ♡
• 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. The spectrum of movement disorders in neurosyphilis: A systematic review. (2026/01/06) ♡
• 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. Cerebrospinal Fluid Biomarkers in Creutzfeldt-Jakob Disease: Diagnostic Value, Limitations, and Future Multi-Omics Strategies. (2026/01/05) ♡
• Description of individual patientsiThe story of one or a couple of patients. Informative, but you cannot infer from it whether something works in general. M232R Familial Creutzfeldt-Jacob Disease Challenging to Diagnose Due to the Absence of Characteristic Laboratory Findings. (2026/01/01) ♡
• Integrated peripheral metabolic and inflammatory biomarker signatures are associated with clinical deterioration in Creutzfeldt-Jakob disease. (2026/01/01) ♡

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