Decade in review--cardiomyopathies: Cardiomyopathy on the move.

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.

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.

Who cites it

10 citing papers in PubMed.

1. Leveraging the shared and opposing genetic mechanisms in the heritable cardiomyopathies.Research square · 2026
   Article
2. Cardiovascular Involvement in PediatricJournal of cardiovascular development and disease · 2022
   Article
3. Towards precision medicine in heart failure.Nature reviews. Cardiology · 2021
   Review
4. Genetic evaluation of cardiomyopathies in Qatar identifies enrichment of pathogenic sarcomere gene variants and possible founder disease mutations in the Arabs.Molecular genetics & genomic medicine · 2021
   Article
5. The p.Ala2430Val mutation in filamin C causes a "hypertrophic myofibrillar cardiomyopathy".Journal of muscle research and cell motility · 2021
   Article
6. An Investigation of Fibulin-2 in Hypertrophic Cardiomyopathy.International journal of molecular sciences · 2020
   Article
7. Cardiac-Specific Cre Induces Age-Dependent Dilated Cardiomyopathy (DCM) in Mice.Molecules (Basel, Switzerland) · 2019
   Article
8. When signalling goes wrong: pathogenic variants in structural and signalling proteins causing cardiomyopathies.Journal of muscle research and cell motility · 2017
   Review
9. Current state of the art and future of myectomy.Annals of cardiothoracic surgery · 2017
   Review
10. Genetic modifiers to the PLN L39X mutation in a patient with DCM and sustained ventricular tachycardia?Global cardiology science & practice · 2015
    Article

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

Authors and funding

1 author.

Funding

No grant is acknowledged in the PubMed record.

Abstract

Indexed as