Evidence map›Paper›PMID 36944446›Full record

ArticleBMJ case reports2023

Abnormal liver function tests and improved survival in a child with splice mutation TARP syndrome.

Michael Lane, Nicholas M Allen, Johannes Letshwiti

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

Article in BMJ case reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed, 1 pooled it
0.5field-weighted citation impact, top 34% 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

1 citing paper in PubMed, 1 synthesis or guideline pooled it, 3 citations in OpenAlex.

  1. Pooled it
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

3 authors at 2 institutions in 1 country.

Michael LanePaediatrics, National University of Ireland, Galway, Ireland.
Nicholas M AllenPaediatrics, Galway University Hospitals, Galway, Ireland.
Johannes LetshwitiPaediatrics, Galway University Hospitals, Galway, Ireland jletshwiti@yahoo.co.uk.
University Hospital Galway · IEOllscoil na Gaillimhe – University of Galway · IE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

TARP (talipes equinovarus, atrial septal defect (ASD), Robin sequence, persistent left superior vena cava) syndrome is a rare X-linked disorder affecting the

Indexed as

ClubfootHeart Septal Defects, AtrialPierre Robin SyndromeHeart Defects, CongenitalHumansLiver Function TestsMaleMutationPhenotypeRNA-Binding ProteinsVena Cava, SuperiorRBM10 protein, humanRNA-Binding ProteinsBilirubin disordersDevelopmental paediatrocsGeneticsNeonatal intensive careParenteral / enteral feeding

Identifiers

PMID36944446
PMCPMC10032413
OpenAlexW4353018892

What OpenQuestion 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 OpenQuestion graph.