Evidence map›Paper›PMID 36874254›Full record

ArticleFrontiers in pediatrics2022

Case Report: A novel

Irina N Artamonova, Anna M Zlotina, Olga R Ismagilova, Tatyana A Levko, Natalia Yu Kolbina, Aleksandr V Bryzzhin, Andrey P Smorodin, Alexandr V Borodin, Ekaterina A Mamaeva, Anna A Sukhotskaya and 5 more

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

Article 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 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.5field-weighted citation impact, top 43% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Pulmonary hypertension associated with nonparenchymal restrictive lung diseases.European respiratory review : an official journal of the European Respiratory Society · 2026
    Review
  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

15 authors at 2 institutions in 1 country.

Irina N ArtamonovaInstitute of Perinatology and Pediatrics, Almazov National Medical Research Centre, Saint-Petersburg, Russia.
Anna M ZlotinaInstitute of Molecular Biology and Genetics, Almazov National Medical Research Centre, Saint-Petersburg, Russia.
Olga R IsmagilovaFederal State Budgetary Scientific Institution, Research Centre for Medical Genetics (RCMG), Moscow, Russia.
Tatyana A LevkoDepartment of Pediatric and Medical Rehabilitation, Almazov National Medical Research Centre, Saint-Petersburg, Russia.
Natalia Yu KolbinaDepartment of Pediatric and Medical Rehabilitation, Almazov National Medical Research Centre, Saint-Petersburg, Russia.
Aleksandr V BryzzhinPediatric Anesthesiology and Intensive Care Unit, Almazov National Medical Research Centre, Saint-Petersburg, Russia.
Andrey P SmorodinPediatric Surgery Anesthesiology and Intensive Care Unit Almazov National Medical Research Centre, Saint-Petersburg, Russia.
Alexandr V BorodinWorld-Class Research Centre for Personalized Medicine, Research Centre of Unknown, Rare and Genetically Determined Diseases, Almazov National Medical Research Centre, Saint-Petersburg, Russia.
Ekaterina A MamaevaInstitute of Perinatology and Pediatrics, Almazov National Medical Research Centre, Saint-Petersburg, Russia.
Anna A SukhotskayaDepartment of Pediatric Surgery for Congenital Malformations, Almazov National Medical Research Centre, Saint-Petersburg, Russia.
Ilya M KagantsovDepartment of Pediatric Surgery for Congenital Malformations, Institute of Perinatology and Pediatrics, Almazov National Medical Research Centre, Saint-Petersburg, Russia.
Daria A MalyshevaDepartment of Pediatric Surgery for Congenital Malformations, Almazov National Medical Research Centre, Saint-Petersburg, Russia.
Elena S VasichkinaWorld-Class Research Centre for Personalized Medicine, Research Centre of Unknown, Rare and Genetically Determined Diseases, Almazov National Medical Research Centre, Saint-Petersburg, Russia.
Tatiana M PervuninaInstitute of Perinatology and Pediatrics, World-Class Research Centre for Personalized Medicine, Research Centre of Unknown, Rare and Genetically Determined Diseases, Almazov National Medical Research Centre, Saint-Petersburg, Russia.
Natalia A PetrovaWorld-Class Research Centre for Personalized Medicine, Research Centre of Unknown, Rare and Genetically Determined Diseases, Institute of Perinatology and Pediatrics, Almazov National Medical Research Centre, Saint-Petersburg, Russia.
Federal Almazov North-West Medical Research Centre · RUResearch Centre for Medical Genetics · RU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Congenital central hypoventilation syndrome (CCHS) is a rare disease characterized by central alveolar hypoventilation and impaired autonomic regulation, caused by pathogenic variants of Case description: We present a clinical case of a girl with a novel Conclusion: Detection of a novel

Indexed as

congenital central hypoventilation syndrome (CCHS)genotype–phenotype correlationHirschsprung diseasenovel mutationPHOX2Bpolyalanine sequence

Identifiers

PMID36874254
PMCPMC9975566
OpenAlexW4320918268

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.