Evidence map›Paper›PMID 36927868›Full record

ArticleOpen heart2023

Late-onset and classic phenotypes of Fabry disease in males with the

Kati Valtola, Marja Hedman, Ilkka Kantola, Susanne Walls, Seppo Helisalmi, Maleeha Maria, Joose Raivo, Christiane Auray-Blais, Johanna Kuusisto

Open access · goldAbstract read
In one paragraph

Article in Open heart, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 2 pooled it
1.6field-weighted citation impact, top 17% 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

8 citing papers in PubMed, 2 syntheses or guidelines pooled it, 9 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. A mulberry in female hypertrophic cardiomyopathy.Oxford medical case reports · 2026
    Article
  4. Article
  5. Article
  6. Review
  7. Review
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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 4 institutions in 2 countries.

Kati ValtolaHeart Center, Kuopio University Hospital, Kuopio, Finland.
Marja HedmanDiagnostic Imaging Center, Kuopio University Hospital, Kuopio, Finland.
Ilkka KantolaDivision of Medicine, Turku University Hospital, Turku, Finland.
Susanne WallsDivision of Medicine, Turku University Hospital, Turku, Finland.
Seppo HelisalmiInstitute of Clinical Medicine, University of Eastern Finland Institute of Clinical Medicine, Kuopio, Finland.
Maleeha MariaFaculty of Health Sciences, A.I.Virtanen Institute, University of Eastern Finland School of Medicine, Kuopio, Finland.
Joose RaivoInstitute of Clinical Medicine, University of Eastern Finland Institute of Clinical Medicine, Kuopio, Finland.
Christiane Auray-BlaisDepartment of Pediatrics, Division of Medical Genetics, Faculty of Medicine and Health Sciences, Universite de Sherbrooke, Sherbrooke, Quebec, Canada.
Johanna KuusistoCentre for Medicine and Clinical Research, Kuopio University Hospital, Kuopio, Finland johanna.kuusisto@kuh.fi.ORCID 0000-0001-6550-3176
University of Eastern Finland · FITurku University Hospital · FIKuopio University Hospital · FIUniversité de Sherbrooke · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo present phenotypic characteristics and biomarkers of a family with the rare mutation Thr410Ala of the METHODS AND

resultsIn a woman in her 60s with hypertrophic cardiomyopathy, T410A/

conclusionsThe T410A/

Indexed as

Cardiomyopathy, HypertrophicFabry Diseasealpha-GalactosidaseFemaleHumansMaleMutationPhenotypealpha-GalactosidaseBiomarkersCardiomyopathy, HypertrophicMetabolic Diseases

Identifiers

PMID36927868
PMCPMC10030781
OpenAlexW4327575281

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.