Evidence map›Paper›PMID 37892364›Full record

ArticleChildren (Basel, Switzerland)2023

Phenotype of Idiopathic Infantile Hypercalcemia Associated with the Heterozygous Pathogenic Variant of

Teofana Otilia Bizerea-Moga, Flavia Chisavu, Cristina Ilies, Orsolya Olah, Otilia Marginean, Mihai Gafencu, Gabriela Doros, Ramona Stroescu

Open access · goldAbstract readCase Reports
In one paragraph

Article in Children (Basel, Switzerland), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

4 citing papers in PubMed, 7 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. 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

8 authors at 1 institution in 1 country.

Teofana Otilia Bizerea-MogaDepartment XI of Pediatrics-1st Pediatric Discipline, Center for Research on Growth and Developmental Disorders in Children, 'Victor Babeș' University of Medicine and Pharmacy Timișoara, Eftimie Murgu Sq. No. 2, 300041 Timișoara, Romania.ORCID 0000-0002-1599-5579
Flavia Chisavu4th Pediatric Clinic, 'Louis Țurcanu' Children's Clinical sand Emergency Hospital, Iosif Nemoianu 2, 300011 Timișoara, Romania.ORCID 0000-0001-9456-4517
Cristina Ilies1st Pediatric Clinic, 'Louis Țurcanu' Children's Clinical and Emergency Hospital, Iosif Nemoianu 2, 300011 Timișoara, Romania.ORCID 0000-0003-4440-5133
Orsolya Olah1st Pediatric Clinic, 'Louis Țurcanu' Children's Clinical and Emergency Hospital, Iosif Nemoianu 2, 300011 Timișoara, Romania.
Otilia MargineanDepartment XI of Pediatrics-1st Pediatric Discipline, Center for Research on Growth and Developmental Disorders in Children, 'Victor Babeș' University of Medicine and Pharmacy Timișoara, Eftimie Murgu Sq. No. 2, 300041 Timișoara, Romania.ORCID 0000-0003-2313-7643
Mihai Gafencu4th Pediatric Clinic, 'Louis Țurcanu' Children's Clinical sand Emergency Hospital, Iosif Nemoianu 2, 300011 Timișoara, Romania.ORCID 0000-0002-9029-5919
Gabriela Doros4th Pediatric Clinic, 'Louis Țurcanu' Children's Clinical sand Emergency Hospital, Iosif Nemoianu 2, 300011 Timișoara, Romania.ORCID 0000-0003-2277-4034
Ramona StroescuDepartment XI of Pediatrics-1st Pediatric Discipline, Center for Research on Growth and Developmental Disorders in Children, 'Victor Babeș' University of Medicine and Pharmacy Timișoara, Eftimie Murgu Sq. No. 2, 300041 Timișoara, Romania.ORCID 0000-0002-4403-0581
Victor Babeș University of Medicine and Pharmacy Timișoara · RO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Idiopathic infantile hypercalcemia (IIH) is a rare genetic disease, also called hypersensitivity to vitamin D3. The molecular heterogeneity allows for the differentiation between the two forms; IIH type 1 caused by

Indexed as

CYP24A1idiopathic infantile hypercalcemianephrocalcinosisSLC34A1

Identifiers

PMID37892364
PMCPMC10605249
OpenAlexW4387701906

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.