Evidence map›Paper›PMID 37189872›Full record

ArticleChildren (Basel, Switzerland)2023

First Reported Case of Gabriele-de Vries Syndrome with Spinal Dysraphism.

Nenad Koruga, Silvija Pušeljić, Marko Babić, Mario Ćuk, Andrea Cvitković Roić, Vjenceslav Vrtarić, Anamarija Soldo Koruga, Alen Rončević, Višnja Tomac, Tatjana Rotim and 5 more

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

Article in Children (Basel, Switzerland), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
4.6field-weighted citation impact, top 6% 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

3 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Article
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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

15 authors at 3 institutions in 2 countries.

Nenad KorugaDepartment of Neurosurgery, University Hospital Center Osijek, 31000 Osijek, Croatia.ORCID 0000-0001-7555-1155
Silvija PušeljićFaculty of Medicine, Josip Juraj Strossmayer University of Osijek, 31000 Osijek, Croatia.
Marko BabićFaculty of Medicine, Josip Juraj Strossmayer University of Osijek, 31000 Osijek, Croatia.
Mario ĆukDepartment of Pediatrics, University Hospital Center Zagreb, 10000 Zagreb, Croatia.
Andrea Cvitković RoićFaculty of Medicine, Josip Juraj Strossmayer University of Osijek, 31000 Osijek, Croatia.ORCID 0000-0003-2003-0656
Vjenceslav VrtarićDepartment of Neurosurgery, University Hospital Center Osijek, 31000 Osijek, Croatia.
Anamarija Soldo KorugaFaculty of Medicine, Josip Juraj Strossmayer University of Osijek, 31000 Osijek, Croatia.
Alen RončevićDepartment of Neurosurgery, University Hospital Center Osijek, 31000 Osijek, Croatia.ORCID 0000-0002-4120-5737
Višnja TomacFaculty of Medicine, Josip Juraj Strossmayer University of Osijek, 31000 Osijek, Croatia.ORCID 0000-0002-3715-8413
Tatjana RotimFaculty of Medicine, Josip Juraj Strossmayer University of Osijek, 31000 Osijek, Croatia.
Tajana TurkFaculty of Medicine, Josip Juraj Strossmayer University of Osijek, 31000 Osijek, Croatia.
Domagoj KretićFaculty of Medicine, Josip Juraj Strossmayer University of Osijek, 31000 Osijek, Croatia.
Nora PušeljićFaculty of Medicine, Josip Juraj Strossmayer University of Osijek, 31000 Osijek, Croatia.
Rebeka NađFaculty of Medicine, Josip Juraj Strossmayer University of Osijek, 31000 Osijek, Croatia.
Ivana SerdarušićFaculty of Medicine, Josip Juraj Strossmayer University of Osijek, 31000 Osijek, Croatia.ORCID 0000-0001-8870-136X
University of Osijek · HRSt. Helena Hospital · USUniversity Hospital Centre Zagreb · HR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Gabriele-de Vries syndrome is a rare autosomal dominant genetic disease caused by de novo pathogenic variants in the

Indexed as

Arnold-Chiari malformationGabriele-de Vries syndromespinal dysraphismwhole-exome sequencingYY1

Identifiers

PMID37189872
PMCPMC10136706
OpenAlexW4361004416

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.