Evidence map›Paper›PMID 38176754›Full record

ArticleBMJ case reports2024

Filamin A gene mutation in an infant with progressive pulmonary emphysema, periventricular nodular heterotopia and congenital heart disease.

Sanjeev Khera, Shilpa Jauhari, Somali Pattanayak, Mrigank Choubey

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

Article in BMJ case reports, 2024. 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, top 100% 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

0 citing papers in PubMed, 0 citations in OpenAlex.

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

4 authors at 3 institutions in 3 countries.

Sanjeev KheraPediatrics, Army Hospital Research and Referral, New Delhi, India kherakherakhera@gmail.com.ORCID 0000-0003-4754-8340
Shilpa JauhariPediatrics, Base Hospital Delhi Cantt, Delhi, India.
Somali PattanayakRadiodiagnosis, Army Hospital Research and Referral, New Delhi, India.
Mrigank ChoubeyPediatrics, Command Hospital Kolkata, Kolkata, West Bengal, India.
Pediatrics and Genetics · USArmy Hospital Research and Referral · INEastern Command Hospital · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Heart Defects, CongenitalPeriventricular Nodular HeterotopiaPulmonary EmphysemaFilaminsHumansInfantMagnetic Resonance ImagingMutationFilaminsCongenital disordersEpilepsy and seizuresGeneticsPaediatric intensive carePulmonary emphysema

Identifiers

PMID38176754
PMCPMC10773292
OpenAlexW4390631496

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.