Evidence map›Paper›PMID 33363936›Full record

ArticleClinical case reports2020

A rare case of pediatric cardiomyopathy: Alström syndrome identified by gene panel analysis.

Valentina Spinelli, Francesca Girolami, Chiara Marrone, Veronica Consigli, Maria Iascone, Silvia Passantino, Giulio Porcedda, Giovanni Battista Calabri, Luciano De Simone, Iacopo Olivotto and 2 more

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

Article in Clinical case reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed, 1 pooled it
0.5field-weighted citation impact, top 28% 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

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

  1. Pooled it
  2. 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

12 authors at 4 institutions in 1 country.

Valentina SpinelliCardiology Unit Meyer Children's Hospital Florence Italy.
Francesca GirolamiCardiology Unit Meyer Children's Hospital Florence Italy.ORCID https://orcid.org/0000-0001-9143-3597
Chiara MarroneDepartment of Cardiology Fondazione Toscana Gabriele Monasterio Massa Italy.
Veronica ConsigliDepartment of Cardiology Fondazione Toscana Gabriele Monasterio Massa Italy.
Maria IasconeDepartment of Genetics ASST Papa Giovanni XXIII Bergamo Italy.
Silvia PassantinoCardiology Unit Meyer Children's Hospital Florence Italy.
Giulio PorceddaCardiology Unit Meyer Children's Hospital Florence Italy.
Giovanni Battista CalabriCardiology Unit Meyer Children's Hospital Florence Italy.
Luciano De SimoneCardiology Unit Meyer Children's Hospital Florence Italy.
Iacopo OlivottoCardiomyopathy Unit University of Florence Florence Italy.
Giuseppe SantoroDepartment of Cardiology Fondazione Toscana Gabriele Monasterio Massa Italy.
Silvia FavilliCardiology Unit Meyer Children's Hospital Florence Italy.
Meyer Children's Hospital · ITFondazione Toscana Gabriele Monasterio · ITOspedale Papa Giovanni XXIII · ITUniversity of Florence · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Genetic investigation of early-onset Dilatative cardiomyopathy phenotype, including molecular autopsy, is the key to appropriate recognition and management of rare etiologies and atypical presentations and to offer genetic counseling to the family.

Indexed as

Alström syndromedilated cardiomyopathynext generation sequencing

Identifiers

PMID33363936
PMCPMC7752570
OpenAlexW3097551251

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.