Evidence map›Paper›PMID 37063861›Full record

ArticleFrontiers in immunology2023

Case report: Schnitzler-like syndrome without monoclonal gammopathy.

Anna Sophie Wesselmann, Axel Künstner, Anke Fähnrich, Christian Rose, Peter Lamprecht, Hauke Busch, Ralf J Ludwig, Andreas Recke

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

Article in Frontiers in immunology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

7 citing papers in PubMed, 14 citations in OpenAlex.

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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

8 authors at 1 institution in 1 country.

Anna Sophie WesselmannDepartment of Dermatology and Allergy, University of Lübeck, Lübeck, Germany.
Axel KünstnerLübeck Institute of Experimental Dermatology, University of Lübeck, Lübeck, Germany.
Anke FähnrichLübeck Institute of Experimental Dermatology, University of Lübeck, Lübeck, Germany.
Christian RoseDepartment of Dermatology and Allergy, University of Lübeck, Lübeck, Germany.
Peter LamprechtDepartment of Rheumatology and Clinical Immunology, University of Lübeck, Lübeck, Germany.
Hauke BuschLübeck Institute of Experimental Dermatology, University of Lübeck, Lübeck, Germany.
Ralf J LudwigLübeck Institute of Experimental Dermatology, University of Lübeck, Lübeck, Germany.
Andreas ReckeDepartment of Dermatology and Allergy, University of Lübeck, Lübeck, Germany.
University of Lübeck · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Schnitzler syndrome is a rare autoinflammatory disorder characterized by urticarial rash, joint pain, recurrent fever, leucocytosis, elevated C-reactive protein (CRP) and serum amyloid A (SAA), and monoclonal IgM or IgG gammopathy. According to the

Indexed as

ExanthemaParaproteinemiasSchnitzler SyndromeSkin DiseasesUrticariaHumansInterleukin 1 Receptor Antagonist ProteinInterleukin 1 Receptor Antagonist Proteinautoinflammationcase reportgammopathylate-onset autoinflammationSchnitzler’s syndrome

Identifiers

PMID37063861
PMCPMC10097979
OpenAlexW4361276995

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.