Evidence map›Paper›PMID 39655047›Full record

ReviewOpen medicine (Warsaw, Poland)2024

Piero Pavone, Xena Giada Pappalardo, Claudia Parano, Raffaele Falsaperla, Antonio Corsello, Enrico Parano, Agata Polizzi, Martino Ruggieri

Abstract readReview
PubMed Full text at PMC Publisher
In one paragraph

Review in Open medicine (Warsaw, Poland), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Intrafamilial Variability inInternational journal of molecular sciences · 2026
    Review
  2. Review
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

8 authors.

Piero PavonePediatrics, and Psychiatric Department of Child and Experimental Medicine, University of Catania, A.O.U. "Policlinico" "G. Rodolico", Catania, Italy.
Xena Giada PappalardoDepartment of Biomedical and Biotechnological Sciences (BIOMETEC), University of Catania, Catania, Italy.
Claudia ParanoDepartment of General Surgery and Medical-Surgical Specialties of the University of Catania, Catania, Italy.
Raffaele FalsaperlaUnit of Pediatrics, Neonatology and Neonatal Intensive Care, and Pediatric Emergency, AOU "Policlinico", PO "San Marco", Catania, Italy.
Antonio CorselloDepartment of Clinical Sciences and Community Health, University of Milan, Milan, Italy.
Enrico ParanoNational Council of Research, Institute for Research and Biomedical Innovation (IRIB), Unit of Catania, Catania, Italy.
Agata PolizziDepartment of Educational Sciences, University of Catania, Catania, Italy.
Martino RuggieriPediatrics, and Psychiatric Department of Child and Experimental Medicine, University of Catania, A.O.U. "Policlinico" "G. Rodolico", Catania, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Methods: Literature review of Results: Our data confirmed that Conclusions: Our present analysis denoted a heterogeneous and unspecific clinical framework of the

Indexed as

NRXN1 geneNRXN1-related disordersPitt-Hopkins syndrome, Pitt-Hopkins-like-syndrome 2seizures

Identifiers

PMID39655047
PMCPMC11627049

What Socratic 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 Socratic graph.