Evidence map›Paper›PMID 39114664›Full record

ReviewFrontiers in immunology2024

Retrospective identification of the first cord blood-transplanted severe aplastic anemia in a

Franz-Martin Fink, Reinhard Höpfl, Martina Witsch-Baumgartner, Gabriele Kropshofer, Sabine Martin, Valentin Fink, Maximilian Heeg, Christina Peters, Johannes Zschocke, Oskar A Haas

Abstract readCase ReportsReview
In one paragraph

Review in Frontiers in immunology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Article
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

10 authors.

Franz-Martin FinkDepartment of Pediatrics, Regional Hospital, St. Johann in Tirol, Austria.
Reinhard HöpflDepartment of Dermatology and Venerology, Medical University Hospital, Innsbruck, Austria.
Martina Witsch-BaumgartnerInstitute of Human Genetics, Medical University, Innsbruck, Austria.
Gabriele KropshoferDepartment of Pediatrics, Medical University Hospital, Innsbruck, Austria.
Sabine MartinDepartment of Pediatrics, Regional Hospital, St. Johann in Tirol, Austria.
Valentin FinkDepartment of Pediatrics, Regional Hospital, St. Johann in Tirol, Austria.
Maximilian HeegInstitute for Immunodeficiency, Center for Chronic Immunodeficiency, Medical Center-University of Freiburg, Faculty of Medicine, University of Freiburg, Freiburg, Germany.
Christina PetersStem Cell Transplantation Unit, St. Anna Children's Hospital, Department of Pediatrics and Adolescent Medicine, Medical University of Vienna, Vienna, Austria.
Johannes ZschockeInstitute of Human Genetics, Medical University, Innsbruck, Austria.
Oskar A HaasCentral Laboratory, St. Anna Children's Hospital, Department of Pediatrics and Adolescent Medicine, Medical University of Vienna, Vienna, Austria.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Severe aplastic anemia (SAA) is a life-threatening bone marrow failure syndrome whose development can be triggered by environmental, autoimmune, and/or genetic factors. The latter comprises germ line pathogenic variants in genes that bring about habitually predisposing syndromes as well as immune deficiencies that do so only occasionally. One of these disorders is the autosomal dominant form of chronic mucocutaneous candidiasis (CMC), which is defined by germ line

Indexed as

Anemia, AplasticCandidiasis, Chronic MucocutaneousSTAT1 Transcription FactorAdultCord Blood Stem Cell TransplantationFemaleHumansMalePedigreeRetrospective StudiesSTAT1 protein, humanSTAT1 Transcription Factorchronic mucocutaneous candidiasis (CMC)gain-of-function pathogenic variantsevere aplastic anemia (SAA)STAT1transplantation

Identifiers

PMID39114664
PMCPMC11303233

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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.