Evidence map›Paper›PMID 34919150›Full record

ArticlePediatric nephrology (Berlin, Germany)2022

Non-lupus full-house nephropathy-immune dysregulation as a rare cause of pediatric nephrotic syndrome: Answers.

Orsolya Horváth, György S Reusz, Veronika Goda, Kata Kelen, István Balogh, Magdolna Kardos, Krisztián Kállay, Áron Cseh, Attila J Szabó, Gergely Kriván

Erratum issuedAbstract read
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In one paragraph

Article in Pediatric nephrology (Berlin, Germany), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors.

Orsolya Horváth1St Department of Pediatrics, Semmelweis University, 53-54 Bókay János Street, Budapest, 1083, Hungary.ORCID http://orcid.org/0000-0002-3812-2711
György S Reusz1St Department of Pediatrics, Semmelweis University, 53-54 Bókay János Street, Budapest, 1083, Hungary. reusz.gyorgy@med.semmelweis-univ.hu.ORCID http://orcid.org/0000-0003-0396-043X
Veronika GodaPediatric Hematology and Stem Cell Transplantation Unit, Central Hospital of Southern Pest, National Institute of Hematology and Infectious Diseases, Budapest, Hungary.ORCID http://orcid.org/0000-0002-0757-538X
Kata Kelen1St Department of Pediatrics, Semmelweis University, 53-54 Bókay János Street, Budapest, 1083, Hungary.ORCID http://orcid.org/0000-0002-1011-1746
István BaloghDepartment of Laboratory Medicine, Division of Clinical Genetics, Department of Human Genetics, Faculty of Medicine, University of Debrecen, Debrecen, Hungary.ORCID http://orcid.org/0000-0003-3397-2829
Magdolna Kardos2Nd Department of Pathology, Semmelweis University, Budapest, Hungary.ORCID http://orcid.org/0000-0003-1464-7887
Krisztián KállayPediatric Hematology and Stem Cell Transplantation Unit, Central Hospital of Southern Pest, National Institute of Hematology and Infectious Diseases, Budapest, Hungary.ORCID http://orcid.org/0000-0002-4328-9612
Áron Cseh1St Department of Pediatrics, Semmelweis University, 53-54 Bókay János Street, Budapest, 1083, Hungary.ORCID http://orcid.org/0000-0003-1659-3173
Attila J Szabó1St Department of Pediatrics, Semmelweis University, 53-54 Bókay János Street, Budapest, 1083, Hungary.ORCID http://orcid.org/0000-0001-7321-9861
Gergely KrivánPediatric Hematology and Stem Cell Transplantation Unit, Central Hospital of Southern Pest, National Institute of Hematology and Infectious Diseases, Budapest, Hungary.ORCID http://orcid.org/0000-0003-4853-4354

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Diabetes Mellitus, Type 1Genetic Diseases, X-LinkedImmune System DiseasesNephrotic SyndromeChildDiarrheaFemaleForkhead Transcription FactorsHumansMaleMutationT-Lymphocytes, RegulatoryForkhead Transcription FactorsAutoimmunityFOXP3 mutation“Full-house” nephropathy (FHN)IPEX syndromePrimary immunodeficiency (PID)

Identifiers

PMID34919150
PMCPMC9023414

What OpenQuestion holds

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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.