Evidence map›Paper›PMID 38179148›Full record

ArticleCase reports in ophthalmology

Two Japanese Families with Pigmented Paravenous Retinochoroidal Atrophy and HK1 Mutation: A Case Report.

Shigeru Sato, Takeshi Morimoto, Takashi Fujikado, Sayaka Tanaka, Sou Sai, Motokazu Tsujikawa, Kohji Nishida

Open access · goldAbstract readCase Reports
In one paragraph

Article in Case reports in ophthalmology. 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
0.5field-weighted citation impact, top 39% of its field
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, 2 citations in OpenAlex.

  1. AnInternational journal of ophthalmology · 2026
    Article
  2. A unilateral presentation of pigmented paravenous chorioretinal atrophy: a case report.Documenta ophthalmologica. Advances in ophthalmology · 2025
    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

7 authors at 1 institution in 1 country.

Shigeru SatoDepartment of Ophthalmology, Osaka University Graduate School of Medicine, Osaka, Japan.
Takeshi MorimotoDepartment of Ophthalmology, Osaka University Graduate School of Medicine, Osaka, Japan.
Takashi FujikadoSpecial Research Promotion Group, Osaka University Graduate School of Frontier Biosciences, Osaka, Japan.
Sayaka TanakaDepartment of Ophthalmology, Osaka University Graduate School of Medicine, Osaka, Japan.
Sou SaiLaboratory of Regenerative Medicine and Development, Osaka University Graduate School of Medicine, Osaka, Japan.
Motokazu TsujikawaDepartment of Ophthalmology, Osaka University Graduate School of Medicine, Osaka, Japan.
Kohji NishidaDepartment of Ophthalmology, Osaka University Graduate School of Medicine, Osaka, Japan.
Osaka University · JP

Funding

Wellcome Trust FC001055
6 · The paper itself

Abstract

Hexokinase 1 (

Indexed as

Hexokinase 1Pigmented paravenous retinochoroidal atrophyRetinitis pigmentosaUltra-widefield fundus imagingWhole-exome sequencing

Identifiers

PMID38179148
PMCPMC10764080
OpenAlexW4390547752

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

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.