Evidence map›Paper›PMID 28220292›Full record

ArticleJournal of neurology2017

Juvenile myoclonic epilepsy and Brugada type 1 ECG pattern associated with (a novel) plakophillin 2 mutation.

Lorenzo Gigli, Giovanni Bertero, Monica Coll Vidal, Anna Iglesias, Oscar Campuzano, Pasquale Striano, Antonio Oliva, Ramon Brugada

Abstract readCase ReportsLetter
PubMed Publisher
In one paragraph

Article in Journal of neurology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Brugada Syndrome: Warning of a Systemic Condition?Frontiers in cardiovascular medicine · 2021
    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.

Lorenzo GigliS.Martino Hospital, Clinic of Cardiovascular Disease, University of Genoa, Largo Rosanna Benzi 10, 16132, Genoa, Italy. loregigli@gmail.com.
Giovanni BerteroS.Martino Hospital, Clinic of Cardiovascular Disease, University of Genoa, Largo Rosanna Benzi 10, 16132, Genoa, Italy.
Monica Coll VidalDepartment of Medical Sciences, School of Medicine, University of Girona, EmiliGrahit 77, 17071, Girona, Spain.
Anna IglesiasCardiovascular Genetics Centre, University of Girona-IDIBGI, Parc Científic UdG, Carrer Pic de Peguera 15, 17003, Girona, Spain.
Oscar CampuzanoDepartment of Medical Sciences, School of Medicine, University of Girona, EmiliGrahit 77, 17071, Girona, Spain.
Pasquale StrianoPediatric Neurology and Muscular Diseases Unit, Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, "G. Gaslini" Institute, University of Genoa, Genoa, Italy.
Antonio OlivaSection of Legal Medicine, Institute of Public Health, Catholic University, Largo F. Vito 1, 00168, Rome, Italy.
Ramon BrugadaCardiovascular Genetics Centre, University of Girona-IDIBGI, Parc Científic UdG, Carrer Pic de Peguera 15, 17003, Girona, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

AdultBrugada SyndromeElectrocardiographyElectroencephalographyFemaleHumansMutationMyoclonic Epilepsy, JuvenilePlakophilinsPKP2 protein, humanPlakophilins

Identifiers

PMID28220292

What OpenQuestion holds

Textmetadata
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.