Evidence map›Paper›PMID 39850771›Full record

ArticleNMC case report journal2024

Two Postmortem Cases of Moyamoya Disease with Different RNF213 p.R4810K Variant Statuses.

Tomo Kinoshita, Natsumi Tamada, Shoko Hara, Maki Mukawa, Hiroshi Shintaku, Motoki Inaji, Yoji Tanaka, Tadashi Nariai, Taketoshi Maehara

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

Article in NMC case report journal, 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. Review
  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

9 authors.

Tomo KinoshitaDepartment of Neurosurgery, Institute of Science Tokyo, Tokyo, Japan.
Natsumi TamadaDepartment of Neurosurgery, Institute of Science Tokyo, Tokyo, Japan.
Shoko HaraDepartment of Neurosurgery, Institute of Science Tokyo, Tokyo, Japan.
Maki MukawaDepartment of Neurosurgery, Institute of Science Tokyo, Tokyo, Japan.
Hiroshi ShintakuDepartment of Pathology, Institute of Science Tokyo, Tokyo, Japan.
Motoki InajiDepartment of Neurosurgery, Institute of Science Tokyo, Tokyo, Japan.
Yoji TanakaDepartment of Neurosurgery, Institute of Science Tokyo, Tokyo, Japan.
Tadashi NariaiDepartment of Neurosurgery, Institute of Science Tokyo, Tokyo, Japan.
Taketoshi MaeharaDepartment of Neurosurgery, Institute of Science Tokyo, Tokyo, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Moyamoya disease (MMD) is characterized by distinct histopathological changes in intracranial arteries, such as narrowing of the arterial lumen due to thickening of the tunica intima, waving of the internal elastic membranes, and thinning of the tunica media. Ring finger protein 213

Indexed as

autopsycerebrovascular disordersmoyamoya diseasepathologyRNF213

Identifiers

PMID39850771
PMCPMC11756894

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.