Evidence map›Paper›PMID 33530632›Full record

ArticleGenes2021

Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy in Two Siblings: Same Mutations but Very Different Phenotypes.

Andrea Carpino, Raffaele Buganza, Patrizia Matarazzo, Gerdi Tuli, Michele Pinon, Pier Luigi Calvo, Davide Montin, Francesco Licciardi, Luisa De Sanctis

Open access · goldAbstract readCase Reports
In one paragraph

Article in Genes, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
2.6field-weighted citation impact, top 9% 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

16 citing papers in PubMed, 1 synthesis or guideline pooled it, 21 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Severity of SARS-CoV-2 infection in children with inborn errors of immunity (primary immunodeficiencies): a systematic review.Allergy, asthma, and clinical immunology : official journal of the Canadian Society of Allergy and Clinical Immunology · 2023
    Article
  8. COVID-19 and Inborn Errors of Immunity.Physiology (Bethesda, Md.) · 2022
    Review
  9. Article
  10. Review
  11. Human autoantibodies underlying infectious diseases.The Journal of experimental medicine · 2022
    Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Review
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

9 authors at 2 institutions in 1 country.

Andrea CarpinoPostgraduate School of Pediatrics, University of Turin, 10126 Turin, Italy.ORCID 0000-0003-2040-9228
Raffaele BuganzaPediatric Endocrinology Unit, Regina Margherita Children's Hospital, 10126 Turin, Italy.
Patrizia MatarazzoPediatric Endocrinology Unit, Regina Margherita Children's Hospital, 10126 Turin, Italy.
Gerdi TuliPediatric Endocrinology Unit, Regina Margherita Children's Hospital, 10126 Turin, Italy.
Michele PinonPediatric Gastroenterology Unit, Regina Margherita Children's Hospital, 10126 Turin, Italy.
Pier Luigi CalvoPediatric Gastroenterology Unit, Regina Margherita Children's Hospital, 10126 Turin, Italy.
Davide MontinPediatric Immunology and Rheumatology, Regina Margherita Children's Hospital, 10126 Turin, Italy.
Francesco LicciardiPediatric Immunology and Rheumatology, Regina Margherita Children's Hospital, 10126 Turin, Italy.
Luisa De SanctisPediatric Endocrinology Unit, Regina Margherita Children's Hospital, 10126 Turin, Italy.
Ospedale Regina Margherita · ITUniversity of Turin · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED), caused by mutations in the

Indexed as

SiblingsAdolescentChildChild, PreschoolCOVID-19FemaleHumansInfantInfant, NewbornMaleMutationPhenotypePolyendocrinopathies, AutoimmuneAIRE geneautoimmune polyendocrinopathy–candidiasis–ectodermal dystrophy (APECED)genotype–phenotype correlation

Identifiers

PMID33530632
PMCPMC7912139
OpenAlexW3125430479

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.