Evidence map›Paper›PMID 38407006›Full record

ArticleJournal of clinical research in pediatric endocrinology2024

Novel

Yurong Piao, Rongmin Li, Yingjie Wang, Congli Chen, Yanmei Sang

Open access · goldAbstract readCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Article in Journal of clinical research in pediatric endocrinology, 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
0.3field-weighted citation impact, top 41% 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, 1 citations in OpenAlex.

  1. 3-M syndrome: evolution of the phenotype over time.Italian journal of pediatrics · 2025
    Review
  2. Review
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

5 authors at 2 institutions in 1 country.

Yurong PiaoNational Center for Children’s Health, Capital Medical University, Beijing Children’s Hospital, Clinic of Immunity, Beijing, ChinaORCID 0009-0008-0267-7257
Rongmin LiBaoding Children’s Hospital, Baoding Key Laboratory of Clinical Research on Children’s Respiratory and Digestive Diseases Bao Ding, Clinic of Endocrinology, Hebei, ChinaORCID 0000-0002-1116-3855
Yingjie WangBaoding Children’s Hospital, Baoding Key Laboratory of Clinical Research on Children’s Respiratory and Digestive Diseases Bao Ding, Clinic of Endocrinology, Hebei, ChinaORCID 0009-0003-1782-0259
Congli ChenNational Center for Children’s Health, Capital Medical University, Beijing Children’s Hospital, Department of Endocrinology, Beijing, ChinaORCID 0009-0001-0997-0682
Yanmei SangNational Center for Children’s Health, Capital Medical University, Beijing Children’s Hospital, Department of Endocrinology, Beijing, ChinaORCID 0000-0002-6213-2661
Beijing Children’s Hospital · CNBaoding People's Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

3M syndrome is an autosomal recessive disorder characterized by short stature and skeletal developmental abnormalities. A Chinese girl with 3M syndrome and a novel

Indexed as

Cytoskeletal ProteinsDwarfismMuscle HypotoniaChild, PreschoolChinaEast Asian PeopleFemaleHumansMuscular AtrophyMutationPiebaldismSpineCytoskeletal ProteinsOBSL1 protein, human3M syndromeintrauterine growth retardationOBSL1 geneShort stature

Identifiers

PMID38407006
PMCPMC11629732
OpenAlexW4392182672

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.