Evidence map›Paper›PMID 37626534›Full record

ArticleBrain sciences2023

Juvenile-Onset Recurrent Rhabdomyolysis Due to Compound Heterozygote Variants in the

Beatrice Labella, Gaetana Lanzi, Stefano Cotti Piccinelli, Filomena Caria, Simona Damioli, Barbara Risi, Enrica Bertella, Loris Poli, Alessandro Padovani, Massimiliano Filosto

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

Article in Brain sciences, 2023. 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
0.4field-weighted citation impact, top 39% 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, 2 citations in OpenAlex.

  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

10 authors at 2 institutions in 1 country.

Beatrice LabellaDepartment of Clinical and Experimental Sciences, University of Brescia, 25100 Brescia, Italy.
Gaetana LanziMedical Genetics Laboratory, Diagnostic Department, ASST-Pedali Civili of Brescia, 25100 Brescia, Italy.
Stefano Cotti PiccinelliDepartment of Clinical and Experimental Sciences, University of Brescia, 25100 Brescia, Italy.
Filomena CariaNeMO-Brescia Clinical Center for Neuromuscular Diseases, 25064 Brescia, Italy.
Simona DamioliNeMO-Brescia Clinical Center for Neuromuscular Diseases, 25064 Brescia, Italy.ORCID 0009-0008-0465-5262
Barbara RisiNeMO-Brescia Clinical Center for Neuromuscular Diseases, 25064 Brescia, Italy.
Enrica BertellaNeMO-Brescia Clinical Center for Neuromuscular Diseases, 25064 Brescia, Italy.
Loris PoliUnit of Neurology, ASST "Spedali Civili", 25100 Brescia, Italy.
Alessandro PadovaniDepartment of Clinical and Experimental Sciences, University of Brescia, 25100 Brescia, Italy.
Massimiliano FilostoDepartment of Clinical and Experimental Sciences, University of Brescia, 25100 Brescia, Italy.ORCID 0000-0002-2852-7512
University of Brescia · ITAzienda Socio Sanitaria Territoriale degli Spedali Civili di Brescia · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Very long-chain acyl-CoA dehydrogenase (VLCAD) deficiency is a rare autosomal recessive long-chain fatty acid oxidation disorder caused by mutations in the

Indexed as

ACADVLlipid myopathymyoglobinuriarhabdomyolysisVLCADVLCADD

Identifiers

PMID37626534
PMCPMC10452278
OpenAlexW4385650436

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.