Evidence map›Paper›PMID 42814028›Full record

ArticleJournal of human immunity2026

Antibody deficiency in myotonic dystrophy type 1: A differential diagnosis below the radar.

Edoardo Galli, Christoph T Berger, Thomas Daikeler, Anne-Kathrin Peyer Kauffmann, Marc Emmenegger, Armin Droll, Andrea Egger, Michael Sinnreich, Mike Recher

Abstract read
In one paragraph

Article in Journal of human immunity, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Edoardo GalliDepartment of Neurology, University and University Hospital of Basel, Basel, Switzerland.ORCID 0000-0002-9760-2643
Christoph T BergerUniversity Center for Immunology, University Hospital Basel , Basel, Switzerland.ORCID 0000-0002-1730-8824
Thomas DaikelerUniversity Center for Immunology, University Hospital Basel , Basel, Switzerland.ORCID 0000-0003-4894-9613
Anne-Kathrin Peyer KauffmannDepartment of Neurology, University and University Hospital of Basel, Basel, Switzerland.ORCID 0009-0007-5180-8607
Marc EmmeneggerDivision of Medical Immunology, Department of Laboratory Medicine, University Hospital Basel, Basel, Switzerland.ORCID 0000-0002-6073-8811
Armin DrollDepartment of Internal Medicine, Regional Hospital Dornach, Dornach, Switzerland.ORCID 0009-0005-8830-8433
Andrea EggerEndocrinology Private Practice , Basel, Switzerland.ORCID 0009-0002-2532-854X
Michael SinnreichDepartment of Neurology, University and University Hospital of Basel, Basel, Switzerland.ORCID 0000-0002-9835-1276
Mike RecherUniversity Center for Immunology, University Hospital Basel , Basel, Switzerland.ORCID 0000-0002-9121-6936

Funding

Swiss Neurological SocietyUniversity Hospital Basel pp 25-06University Hospital Basel pp 25-24
6 · The paper itself

Abstract

Myotonic dystrophy type 1 is a rare, underdiagnosed genetic neuromuscular disorder that is often accompanied by hypogammaglobulinemia, serving as a crucial diagnostic clue. We report the clinical and immunophenotypic features of two patients and discuss the underlying pathogenesis.

Identifiers

PMID42814028
PMCPMC13625849

What OpenQuestion holds

Textmetadata
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Registered trials

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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.