Evidence map›Paper›PMID 34513771›Full record

ArticleFrontiers in pediatrics2021

Novel

Yanyan Cao, Lingzhi Meng, Yudong Zhang, Jiancheng Jiao, Weicong Pu, Li Ma

Abstract readCase Reports
In one paragraph

Article in Frontiers in pediatrics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Article
  3. Novel homozygousMolecular genetics and metabolism reports · 2023
    Article
  4. 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

6 authors.

Yanyan CaoInstitute of Pediatric Research, Children's Hospital of Hebei Province, Shijiazhuang, China.
Lingzhi MengDepartment of Neonatology, Children's Hospital of Hebei Province, Shijiazhuang, China.
Yudong ZhangDepartment of Neonatology, Children's Hospital of Hebei Province, Shijiazhuang, China.
Jiancheng JiaoDepartment of Neonatology, Children's Hospital of Hebei Province, Shijiazhuang, China.
Weicong PuDepartment of Neonatology, Children's Hospital of Hebei Province, Shijiazhuang, China.
Li MaDepartment of Neonatology, Children's Hospital of Hebei Province, Shijiazhuang, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nonketotic hyperglycinemia (NKH) is a lethal autosomal recessive disease resulting from alterations in glycine metabolism, commonly caused by mutations in glycine decarboxylase (

Indexed as

compound heterozygous variantGLDC variationglycine cleavage enzyme systeminherited metabolic diseasenonketotic hyperglycinemia

Identifiers

PMID34513771
PMCPMC8432289

What OpenQuestion holds

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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.