Evidence map›Paper›PMID 41899319›Full record

ArticleJournal of clinical medicine2026

Modifier-Sensitive Phenotypic Divergence in XMEN Disease (MAGT1 Deficiency): Neurodegenerative and Immuno-Hematologic Trajectories.

Ragip Fatih Kural, Zuleyha Galata, Reyhan Gumusburun, Ceyda Tunakan Dalgic, Nur Soyer, Havva Yazıcı, Ayse Nur Yuceyar, Aslı Subasıoglu, Irem Evcili, Bilgi Gungor and 4 more

Abstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Journal of clinical medicine, 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

14 authors.

Ragip Fatih KuralDivision of Allergy and Immunology, Department of Internal Medicine, Ege University Faculty of Medicine, Izmir 35100, Türkiye.
Zuleyha GalataDivision of Allergy and Immunology, Department of Internal Medicine, Ege University Faculty of Medicine, Izmir 35100, Türkiye.ORCID 0000-0001-9627-4281
Reyhan GumusburunDivision of Allergy and Immunology, Department of Internal Medicine, Ege University Faculty of Medicine, Izmir 35100, Türkiye.
Ceyda Tunakan DalgicDivision of Allergy and Immunology, Department of Internal Medicine, Ege University Faculty of Medicine, Izmir 35100, Türkiye.
Nur SoyerDivision of Hematology, Department of Internal Medicine, Ege University Faculty of Medicine, Izmir 35100, Türkiye.ORCID 0000-0002-7722-506X
Havva YazıcıDivision of Pediatric Metabolism, Department of Pediatrics, Ege University Faculty of Medicine, Izmir 35100, Türkiye.ORCID 0000-0002-2564-7420
Ayse Nur YuceyarDepartment of Neurology, Ege University Faculty of Medicine, Izmir 35100, Türkiye.
Aslı SubasıogluDepartment of Medical Genetics, Atatürk Training and Research Hospital, Izmir Katip Celebi University, Izmir 35360, Türkiye.
Irem EvciliIzmir Biomedicine and Genome Center (IBG), Dokuz Eylül University, Izmir 35330, Türkiye.
Bilgi GungorIzmir Biomedicine and Genome Center (IBG), Dokuz Eylül University, Izmir 35330, Türkiye.
Kasım OkanDivision of Allergy and Immunology, Department of Internal Medicine, Ege University Faculty of Medicine, Izmir 35100, Türkiye.
Mehmet SoyluDepartment of Microbiology, Ege University Faculty of Medicine, Izmir 35100, Türkiye.ORCID 0000-0002-9145-1506
Cihat UzunkopruDepartment of Neurology, Atatürk Training and Research Hospital, Izmir Katip Celebi University, Izmir 35360, Türkiye.
Omur ArdenizDivision of Allergy and Immunology, Department of Internal Medicine, Ege University Faculty of Medicine, Izmir 35100, Türkiye.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

EBV-driven lymphomaimmunohematologyinborn errors of immunityMAGT1 deficiencyneurodegenerationtailored surveillancethrombotic microangiopathyXMEN disease

Identifiers

PMID41899319
PMCPMC13028072

What Socratic 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 Socratic graph.