Evidence map›Paper›PMID 36619513›Full record

ReviewFrontiers in pediatrics2022

Biological treatments for pediatric Netherton syndrome.

Matteo Pontone, Mattia Giovannini, Cesare Filippeschi, Teresa Oranges, Fausto Andrea Pedaci, Francesca Mori, Simona Barni, Federica Barbati, Filippo Consonni, Giuseppe Indolfi and 4 more

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in pediatrics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
2.3field-weighted citation impact, top 11% 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

15 citing papers in PubMed, 1 synthesis or guideline pooled it, 23 citations in OpenAlex.

  1. Gene variants associated with skin barrier dysfunction in atopic dermatitis: a systematic review and meta-analysis.Revista paulista de pediatria : orgao oficial da Sociedade de Pediatria de Sao Paulo · 2025
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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

14 authors at 3 institutions in 2 countries.

Matteo PontoneDepartment of Health Sciences, University of Florence, Florence, Italy.
Mattia GiovanniniDepartment of Health Sciences, University of Florence, Florence, Italy.
Cesare FilippeschiDermatology Unit, Department of Pediatrics, Meyer Children's Hospital, Florence, Italy.
Teresa OrangesDermatology Unit, Department of Pediatrics, Meyer Children's Hospital, Florence, Italy.
Fausto Andrea PedaciDepartment of Health Sciences, University of Florence, Florence, Italy.
Francesca MoriAllergy Unit, Department of Pediatrics, Meyer Children's Hospital, Florence, Italy.
Simona BarniAllergy Unit, Department of Pediatrics, Meyer Children's Hospital, Florence, Italy.
Federica BarbatiDepartment of Health Sciences, University of Florence, Florence, Italy.
Filippo ConsonniDepartment of Health Sciences, University of Florence, Florence, Italy.
Giuseppe IndolfiPediatric and Liver Unit, Meyer Children's University Hospital, Florence, Italy.
Lorenzo LodiDepartment of Health Sciences, University of Florence, Florence, Italy.
Chiara AzzariDepartment of Health Sciences, University of Florence, Florence, Italy.
Silvia RicciDepartment of Health Sciences, University of Florence, Florence, Italy.
Alain HovnanianINSERM UMR 1163, Laboratory of Genetic Skin Diseases, Imagine Institute and University of Paris, Paris, France.
University of Florence · ITMeyer Children's Hospital · ITInstitut des Maladies Génétiques Imagine · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Netherton syndrome (NS) is a rare and potentially life-threatening genetic skin disease responsible for skin inflammation and scaling, hair abnormalities and severe allergic manifestations. NS is caused by loss-of-function variants in Serine Peptidase Inhibitor Kazal-Type 5 (

Indexed as

allergologybiological treatmentsdermatologyimmunologyNetherton syndromepediatrics

Identifiers

PMID36619513
PMCPMC9822572
OpenAlexW4312173969

What OpenQuestion 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 OpenQuestion graph.