25 results for “creutzfeldt-jakob”. Showing 25 of 39,449.
Updated clinical diagnostic criteria for sporadic Creutzfeldt-Jakob disease.
Creutzfeldt-Jakob disease. Patients with sporadic Creutzfeldt-Jakob disease and fluid
The Central Role of Actin in Creutzfeldt-Jakob Disease: Unlocking Therapeutic Pathways.
Creutzfeldt-Jakob disease (CJD) is a prion-caused condition characterized
Genome-wide study links MTMR7 gene to variant Creutzfeldt-Jakob risk.
Creutzfeldt-Jakob disease (vCJD) susceptibility. A genome-wide association analysis
Tau pathology in Creutzfeldt-Jakob disease revisited.
Creutzfeldt-Jakob disease (CJD) is a human prion disease with
Creutzfeldt-Jakob disease: A comprehensive review of current understanding and research.
Creutzfeldt-Jakob Disease (CJD) is one of the sample prion
Differential astrocyte and oligodendrocyte vulnerability in murine Creutzfeldt-Jakob disease.
Creutzfeldt-Jakob disease (CJD) using the tg340 mouse line expressing
Abnormal prion protein, infectivity and neurofilament light-chain in blood of macaques with experimental variant Creutzfeldt-Jakob disease.
Creutzfeldt-Jakob disease (vCJD) and sporadic CJD (sCJD) are human
Creutzfeldt-Jakob disease after COVID-19: infection-induced prion protein misfolding? A case report.
Creutzfeldt-Jakob disease (CJD) is a rare, fatal disease presenting
Risk factors for variant Creutzfeldt-Jakob disease in dental practice: a case-control study.
Creutzfeldt-Jakob Disease (vCJD) associated with dental treatment. Case-control
Neuropathological and genetic characteristics of a post-mortem series of cases with dementia with Lewy bodies clinically suspected of Creutzfeldt-Jakob's disease.
Creutzfeldt-Jakob's disease (CJD). To better understand factors contributing
Identification of novel risk loci and causal insights for sporadic Creutzfeldt-Jakob disease: a genome-wide association study.
Creutzfeldt-Jakob disease (sCJD). Variants in the PRNP gene that
Multiomic analyses direct hypotheses for Creutzfeldt-Jakob disease risk genes.
Creutzfeldt-Jakob disease (sCJD). Aside from variation of the prion
Treatment with efavirenz extends survival in a Creutzfeldt-Jakob disease model by regulating brain cholesterol metabolism.
Creutzfeldt-Jakob disease (sCJD) is the most prevalent prion disease
Correlation of striatal dopamine transporter imaging with post mortem substantia nigra cell counts.
Creutzfeldt-Jakob disease (n = 1). [(12) (3) I]β-CIT SPECT
Highly infectious prions generated by a single round of microplate-based protein misfolding cyclic amplification.
Creutzfeldt-Jakob disease. This new format should help in developing
Genetic risk factors for Creutzfeldt-Jakob disease.
Creutzfeldt-Jakob disease (sCJD), is characterized by the seemingly spontaneous
Dysfunction of the cardiac parasympathetic system in fatal familial insomnia: a heart rate variability study.
Creutzfeldt-Jakob disease (CJD). This study enrolled nine patients with
Spontaneous generation of rapidly transmissible prions in transgenic mice expressing wild-type bank vole prion protein.
Creutzfeldt-Jakob disease (CJD), in which prions are formed spontaneously
Creutzfeldt-Jakob disease and other prion diseases.
Prion diseases share common clinical and pathological characteristics such as
Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17.
Creutzfeldt-Jakob disease, motor neuron disease and Alzheimer's disease
Blood Neurofilament Light Chain in Different Types of Dementia.
Creutzfeldt-Jakob disease (CJD) and Lewy body dementia (LBD). Meta
Iron and Ferroptosis More than a Suspect: Beyond the Most Common Mechanisms of Neurodegeneration for New Therapeutic Approaches to Cognitive Decline and Dementia.
Creutzfeldt-Jakob's disease, and amyotrophic lateral sclerosis. These are progressive
Comparing anti-aging hallmark activities of Metformin and Nano-PSO in a mouse model of genetic Creutzfeldt-Jakob Disease.
Advanced age is the main risk factor for the manifestation
Neuropathology and emerging biomarkers in corticobasal syndrome.
Creutzfeldt-Jakob disease) and cerebrovascular disease, based on a narrative
Prion protein amplification techniques.
Creutzfeldt-Jakob disease (sCJD) and has now been included in the diagnostic