Evidence map›Paper›PMID 42359808›Full record

ArticleThe Journal of international medical research2026

Clinical features of dentatorubral-pallidoluysian atrophy: A survey of Chinese patients.

Na Zheng, Miao Li, Yun-Xia Wang, Guo-En Yao

Abstract read
In one paragraph

Article in The Journal of international medical research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

4 authors.

Na Zheng*These authors contributed equally to this work.
Miao Li*These authors contributed equally to this work.
Yun-Xia Wang

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

ObjectiveWe aimed to characterize the clinical, magnetic resonance imaging, and genetic features of Chinese patients with dentatorubral-pallidoluysian atrophy.MethodsIn this retrospective case-series and literature-review study, we analyzed three affected members belonging to the same family diagnosed at our institution. We also reviewed genetically confirmed Chinese dentatorubral-pallidoluysian atrophy cases reported in the China National Knowledge Infrastructure, Wanfang, and PubMed databases up to 31 May 2025 and included additional 42 patients from separate families. Cases with available age at onset, initial symptoms, and CAG repeat size were included; cases without magnetic resonance imaging data were excluded only from imaging-specific analyses. Thus, the final cohort included 45 Chinese dentatorubral-pallidoluysian atrophy patients.ResultsForty-five patients were analyzed. The median

Indexed as

Myoclonic Epilepsies, ProgressiveNerve Tissue ProteinsSeizuresAdolescentAdultAgedAge of OnsetChildChild, PreschoolChinaEast Asian PeopleFemaleHumansMagnetic Resonance ImagingMaleMiddle Agedatrophin-1Nerve Tissue ProteinsATN1Chinadentatorubral–pallidoluysian atrophyepilepsymagnetic resonance imagingretrospective study

Identifiers

PMID42359808
PMCPMC13309664

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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.