Evidence map›Paper›PMID 36620461›Full record

ArticleFrontiers in neuroscience2022

Clinical and genetic analyses of premature mitochondrial encephalopathy with epilepsia partialis continua caused by novel biallelic

Wenjing Hu, Hongjun Fang, Yu Peng, Li Li, Danni Guo, Jingwen Tang, Jurong Yi, Qingqing Liu, Wei Qin, Liwen Wu and 1 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in neuroscience, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.9field-weighted citation impact, top 28% 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

6 citing papers in PubMed, 8 citations in OpenAlex.

  1. Neonatal diabetes mellitus is a significant feature of COXPD-24 caused by recessive NARS2 variants.Diabetic medicine : a journal of the British Diabetic Association · 2025
    Article
  2. Compound heterozygous variants of theFrontiers in pediatrics · 2025
    Article
  3. Article
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  5. Review
  6. 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

11 authors at 1 institution in 1 country.

Wenjing HuDepartment of Neurology, Hunan Children's Hospital, Changsha, China.
Hongjun FangDepartment of Neurology, Hunan Children's Hospital, Changsha, China.
Yu PengPediatrics Research Institute of Hunan Province, Hunan Children's Hospital, Changsha, China.
Li LiDepartment of Radiology, Hunan Children's Hospital, Changsha, China.
Danni GuoDepartment of Neurology, Hunan Children's Hospital, Changsha, China.
Jingwen TangDepartment of Neurology, Hunan Children's Hospital, Changsha, China.
Jurong YiDepartment of Neurology, Hunan Children's Hospital, Changsha, China.
Qingqing LiuDepartment of Neurology, Hunan Children's Hospital, Changsha, China.
Wei QinDepartment of Neurology, Hunan Children's Hospital, Changsha, China.
Liwen WuDepartment of Neurology, Hunan Children's Hospital, Changsha, China.
Zeshu NingDepartment of Neurology, Hunan Children's Hospital, Changsha, China.
Hunan Children's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Biallelic

Indexed as

aminoacylation reactionCOXPD24gene testingminigenemitochondrial diseaseNARS2

Identifiers

PMID36620461
PMCPMC9811187
OpenAlexW4313466030

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.