ArticleJugan geon-gang gwa jilbyeong2023
Article in Jugan geon-gang gwa jilbyeong, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
1 citing paper in PubMed.
- Prion Diseases-When Proteins Turn Lethal: Creutzfeldt-Jakob Disease (CJD) and the Quest for Classification, Diagnosis, Therapeutic Approaches, and Emerging Research.Molecules (Basel, Switzerland) · 2026Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
4 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Creutzfeldt-Jakob disease (CJD) is an infectious prion disease caused by the accumulation of misfolded prion proteins in the central nervous system. It is associated cognitive impairment and ataxia, and results in death within several months after the onset. CJD is subdivided into sporadic, genetic, and acquired types according to the phenotype, epidemiological features, and pathogenesis. Laboratory diagnosis of CJD offers the advantage of being autopsy-free and is essential for accurate diagnosis of the disease along with assessment of clinical symptoms and electroencephalography. In addition, since the incidence of CJD is increasing worldwide, including in the Republic of Korea, the importance of laboratory diagnosis of the disease is also increasing. The 14-3-3 protein analysis, real-time quaking-induced conversion (RT-QuIC), prion protein (
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.