Evidence map›Paper›PMID 41401950›Full record

ReviewZhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics2025

[Comprehensive considerations for the diagnosis, treatment, and management of osteogenesis imperfecta].

Xiang-Hong Lyu, Jian Dong

Abstract readReviewEnglish Abstract
PubMed Full text at PMC Publisher
In one paragraph

Review in Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics, 2025. 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

2 authors.

Xiang-Hong LyuDepartment of Pediatrics, Qingdao Central Hospital, University of Health and Rehabilitation Sciences/Qingdao Central Hospital, Qingdao, Shandong 266000, China.
Jian DongDepartment of Pediatrics, Qingdao Central Hospital, University of Health and Rehabilitation Sciences/Qingdao Central Hospital, Qingdao, Shandong 266000, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Osteogenesis imperfecta (OI) is a rare genetic skeletal disorder most commonly caused by variants in

Indexed as

Collagen Type IFractures, BoneOsteogenesis ImperfectaBone Density Conservation AgentsCollagen Type I, alpha 1 ChainEarly DiagnosisFemaleGenetic Association StudiesGenetic TestingGenetic TherapyHuman Growth HormoneHumansMesenchymal Stem Cell TransplantationMutationPrecision MedicinePregnancyBone Density Conservation AgentsCOL1A1 protein, humanCOL1A2 protein, humanCollagen Type ICollagen Type I, alpha 1 ChainHuman Growth HormoneGenotype-phenotype analysisOsteogenesis imperfectaRecombinant human growth hormone

Identifiers

PMID41401950
PMCPMC12708070

What Socratic holds

Textmetadata
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 Socratic graph.