Evidence map›Paper›PMID 38767731›Full record

ArticleActa neuropathologica2024

Transmission experiments verify sporadic V2 prion in a patient with E200K mutation.

Hitaru Kishida, Atsushi Kobayashi, Kenta Teruya, Hiroshi Doi, Naohisa Ueda, Fumiaki Tanaka, Yoshiyuki Kuroiwa, Piero Parchi, Shirou Mohri, Tetsuyuki Kitamoto

Abstract readCase ReportsLetter
PubMed Full text at PMC Publisher
In one paragraph

Article in Acta neuropathologica, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. E200K genetic Creutzfeldt-Jakob disease with codon 129 MV heterozygosity presenting with a V2-like phenotype: a case report.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2026
    Article
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Hitaru KishidaDepartment of Neurology, Yokohama City University Medical Center, Yokohama, Japan.
Atsushi KobayashiDepartment of Biomedical Models, Graduate School of Biomedical Sciences, Nagasaki University, Nagasaki, Japan.
Kenta TeruyaDepartment of Neurochemistry, Tohoku University Graduate School of Medicine, Sendai, Japan.
Hiroshi DoiDepartment of Neurology and Stroke Medicine, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
Naohisa UedaDepartment of Neurology, Yokohama City University Medical Center, Yokohama, Japan.
Fumiaki TanakaDepartment of Neurology and Stroke Medicine, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
Yoshiyuki KuroiwaDepartment of Neurology, Teikyo University School of Medicine University Hospital, Kawasaki, Japan.
Piero ParchiDepartment of Biomedical and Neuromotor Sciences, University of Bologna, Bologna, Italy.
Shirou MohriOffice for Research Initiatives and Development, Nagasaki University, Japan, Nagasaki.
Tetsuyuki KitamotoDepartment of Neurological Science, Tohoku University Graduate School of Medicine, 2-1, Seiryo-machi, Aoba-ku, Sendai, Miyagi-ken, 980-8575, Japan. kitamoto@med.tohoku.ac.jp.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

MutationPrionsBrainHumansPrion DiseasesPrions

Identifiers

PMID38767731
PMCPMC11106143

What OpenQuestion holds

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Registered trials

None linked

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.