Evidence map›Paper›PMID 34317245›Full record

ArticleJACC. Case reports2020

Novel

M Scott Binder, Emily Brown, Thomas Aversano, Kathryn R Wagner, Hugh Calkins, Andreas S Barth

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

Article in JACC. Case reports, 2020. 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
0.4field-weighted citation impact, top 35% 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

6 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. The FHL1 myopathy spectrum revisited: a literature review and report of two new patients.Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology · 2024
    Review
  5. Review
  6. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 3 institutions in 1 country.

M Scott BinderDepartment of Medicine, Johns Hopkins Bayview Medical Center, Johns Hopkins University, Baltimore, Maryland.
Emily BrownDivision of Cardiology, Department of Medicine, The Johns Hopkins Hospital, Johns Hopkins University, Baltimore, Maryland.
Thomas AversanoDivision of Cardiology, Department of Medicine, The Johns Hopkins Hospital, Johns Hopkins University, Baltimore, Maryland.
Kathryn R WagnerCenter of Genetic Muscle Disease, Kennedy Krieger Institute, Baltimore, Maryland.
Hugh CalkinsDivision of Cardiology, Department of Medicine, The Johns Hopkins Hospital, Johns Hopkins University, Baltimore, Maryland.
Andreas S BarthDivision of Cardiology, Department of Medicine, The Johns Hopkins Hospital, Johns Hopkins University, Baltimore, Maryland.
Johns Hopkins University · USJohns Hopkins Hospital · USJohns Hopkins Medicine · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A 24-year-old man with muscle cramps and a family history of sudden death presented with palpitations. Electrocardiography showed signs of left ventricular hypertrophy and nonsustained ventricular tachycardia, and imaging studies confirmed hypertrophic cardiomyopathy. Genetic testing revealed a novel

Indexed as

cardiomyopathychest paincongenital heart defectEDMD, Emery-Dreifuss muscular dystrophyelectrophysiologygenetic disordersHCM, hypertrophic cardiomyopathyICD, implantable cardioverter-defibrillatorNSVT, nonsustained ventricular tachycardiaSCD, sudden cardiac death

Identifiers

PMID34317245
PMCPMC8311586
OpenAlexW3008400042

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.