Evidence map›Paper›PMID 40649786›Full record

ArticleInternational journal of molecular sciences2025

Impact of Somatic Development and Course of Osteogenesis Imperfecta on FGF23 Levels in Children.

Agnieszka Byrwa-Sztaba, Elżbieta Jakubowska-Pietkiewicz

Abstract read
In one paragraph

Article in International journal of molecular sciences, 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.

Agnieszka Byrwa-SztabaDepartment of Pediatrics, Neonatal Pathology and Metabolic Bone Diseases of Medical University of Lodz, 91-738 Lodz, Poland.ORCID 0000-0002-0610-9897
Elżbieta Jakubowska-PietkiewiczDepartment of Pediatrics, Neonatal Pathology and Metabolic Bone Diseases of Medical University of Lodz, 91-738 Lodz, Poland.

Funding

Medical University of Lodz 503/1-090-02/503-11-001
6 · The paper itself

Abstract

Osteogenesis imperfecta (OI) is a rare bone dysplasia that occurs with a frequency of 1/15,000-20,000 live births. It is characterized by increased susceptibility of bone fractures, skeletal deformities, low stature, and low bone mass. It results in impaired production of type I collagen. About 90% of people with OI have heterozygous mutations in the

Indexed as

Fibroblast Growth FactorsOsteogenesis ImperfectaAdolescentBone DensityChildChild, PreschoolFemaleFibroblast Growth Factor-23Fractures, BoneHumansMalePamidronateFGF23 protein, humanFibroblast Growth Factor-23Fibroblast Growth FactorsPamidronatechildrenFGF23osteogenesis imperfectasomatic development

Identifiers

PMID40649786
PMCPMC12249719

What Socratic holds

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LicenceCC BY
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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.