Evidence map›Paper›PMID 36726751›Full record

ArticleFrontiers in neurology2022

Phenotypic variability within the desminopathies: A case series of three patients.

Dennis Yeow, Matthew Katz, Robert Henderson, Sandhir Prasad, Russell Denman, Stefan Blum, Mark Davis, Thomas Robertson, Pamela McCombe

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

Article in Frontiers in neurology, 2022. 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
0.4field-weighted citation impact, top 39% 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, 2 citations in OpenAlex.

  1. Natural History, Phenotype Spectrum, and Clinical Outcomes of Desmin (Circulation. Genomic and precision medicine · 2025
    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

9 authors at 5 institutions in 1 country.

Dennis YeowDepartment of Neurology, Royal North Shore Hospital, Sydney, NSW, Australia.
Matthew KatzDepartment of Neurology, Royal Brisbane and Women's Hospital, Brisbane, QLD, Australia.
Robert HendersonDepartment of Neurology, Royal Brisbane and Women's Hospital, Brisbane, QLD, Australia.
Sandhir PrasadDepartment of Cardiology, Royal Brisbane and Women's Hospital, Brisbane, QLD, Australia.
Russell DenmanDepartment of Cardiology, The Prince Charles Hospital, Brisbane, QLD, Australia.
Stefan BlumDepartment of Neurology, Princess Alexandra Hospital, Brisbane, QLD, Australia.
Mark DavisDepartment of Diagnostic Genomics, Pathwest Laboratory Medicine, Perth, WA, Australia.
Thomas RobertsonDepartment of Pathology, Royal Brisbane and Women's Hospital, Brisbane, QLD, Australia.
Pamela McCombeDepartment of Neurology, Royal Brisbane and Women's Hospital, Brisbane, QLD, Australia.
Royal Brisbane and Women's Hospital · AUPathwest Laboratory Medicine · AUPrince Charles Hospital · AUPrincess Alexandra Hospital · AURoyal North Shore Hospital · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The

Indexed as

cardiomyopathydesmindesminopathymyofibrillar myopathysplice-site mutation

Identifiers

PMID36726751
PMCPMC9884684
OpenAlexW4316363332

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.