Evidence map›Paper›PMID 31309180›Full record

ArticleActa myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology2019

Cardiac diseases as a predictor warning of hereditary muscle diseases. The case of laminopathies.

Paola D'Ambrosio, Roberta Petillo, Annalaura Torella, Andrea Antonio Papa, Alberto Palladino, Chiara Orsini, Manuela Ergoli, Luigia Passamano, Antonio Novelli, Vincenzo Nigro and 1 more

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

Article in Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed, 1 pooled it
0.2field-weighted citation impact, top 48% 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, 1 synthesis or guideline pooled it, 3 citations in OpenAlex.

  1. Pooled it
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

11 authors at 1 institution in 1 country.

Paola D'AmbrosioCardiomiology and Medical Genetics, Department of Experimental Medicine, University of Campania "Luigi Vanvitelli", Naples, Italy.
Roberta PetilloCardiomiology and Medical Genetics, Department of Experimental Medicine, University of Campania "Luigi Vanvitelli", Naples, Italy.
Annalaura TorellaLaboratory of Medical Genetics, Department of Precisin Medicine, University of Campania "Luigi Vanvitelli", Naples, Italy.
Andrea Antonio PapaArrhythmology Unit, Department of Translational Medical Sciences, University of Campania "Luigi Vanvitelli", Naples, Italy.
Alberto PalladinoCardiomiology and Medical Genetics, Department of Experimental Medicine, University of Campania "Luigi Vanvitelli", Naples, Italy.
Chiara OrsiniCardiomiology and Medical Genetics, Department of Experimental Medicine, University of Campania "Luigi Vanvitelli", Naples, Italy.
Manuela ErgoliCardiomiology and Medical Genetics, Department of Experimental Medicine, University of Campania "Luigi Vanvitelli", Naples, Italy.
Luigia PassamanoCardiomiology and Medical Genetics, Department of Experimental Medicine, University of Campania "Luigi Vanvitelli", Naples, Italy.
Antonio NovelliLaboratory of Medical Genetics, OPBG, Rome, Italy.
Vincenzo NigroLaboratory of Medical Genetics, Department of Precisin Medicine, University of Campania "Luigi Vanvitelli", Naples, Italy.
Luisa PolitanoCardiomiology and Medical Genetics, Department of Experimental Medicine, University of Campania "Luigi Vanvitelli", Naples, Italy.
University of Campania "Luigi Vanvitelli" · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mutations in the

Indexed as

AdolescentAdultFemaleHeart DiseasesHumansLamin Type AMaleMiddle AgedMuscular DiseasesMutationPedigreeYoung AdultLamin Type ALMNA protein, humangenetic counsellinglaminopathiesrisk stratification

Identifiers

PMID31309180
PMCPMC6598412
OpenAlexW2947159268

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.