Evidence map›Paper›PMID 41099604›Full record

ArticlePediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society

Prenatal Isolated Congenital Diaphragmatic Hernia: A Rare Clinical Presentation of a

Nea Tulonen, Jussi Tallus, Heidi Kaprio, Jukka Laine, Mirjami Mattila, Maria Haanpää, Sini Keskinen

Abstract readCase Reports
In one paragraph

Article in Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

7 authors.

Nea TulonenTyks Laboratories, Genomics, Clinical Genetics, TYKS Turku University Hospital, Finland.ORCID 0009-0001-4686-4213
Jussi TallusUniversity of Turku, Finland.ORCID 0000-0001-6425-5254
Heidi KaprioUniversity of Turku, Finland.ORCID 0000-0001-5706-1718
Jukka LaineUniversity of Turku, Finland.ORCID 0000-0003-4330-0030
Mirjami MattilaUniversity of Turku, Finland.ORCID 0000-0002-3124-3908
Maria HaanpääTyks Laboratories, Genomics, Clinical Genetics, TYKS Turku University Hospital, Finland.
Sini KeskinenTyks Laboratories, Genomics, Clinical Genetics, TYKS Turku University Hospital, Finland.ORCID 0000-0001-5689-825X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Congenital diaphragmatic hernia is a genetically heterogeneous condition with a developmental defect in the diaphragm. The

Indexed as

GATA4 Transcription FactorHernias, Diaphragmatic, CongenitalCodon, NonsenseFemaleHaploinsufficiencyHumansPregnancyUltrasonography, PrenatalCodon, NonsenseGATA4 protein, humanGATA4 Transcription Factordiaphragmatic herniafetalGATA4prenatal

Identifiers

PMID41099604
PMCPMC12779761

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.