Evidence map›Paper›PMID 35410112›Full record

ArticleJournal of clinical research in pediatric endocrinology2023

Neonatal Diabetes, Congenital Hypothyroidism, and Congenital Glaucoma Coexistence: A Case of

Emre Sarıkaya, Mustafa Kendirci, Mikail Demir, Munis Dündar

Abstract readCase Reports
In one paragraph

Article in Journal of clinical research in pediatric endocrinology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
–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

10 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. A Novel Renal Manifestation inJournal of medical cases · 2026
    Article
  3. Article
  4. Review
  5. Review
  6. Neonatal and Syndromic Forms of Diabetes.Current diabetes reports · 2025
    Review
  7. Article
  8. Neonatal diabetes mellitus around the world: Update 2024.Journal of diabetes investigation · 2024
    Review
  9. Article
  10. 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

4 authors.

Emre SarıkayaErciyes University Faculty of Medicine, Department of Pediatric Endocrinology, Kayseri, TurkeyORCID 0000-0002-7355-5408
Mustafa KendirciErciyes University Faculty of Medicine, Department of Pediatric Endocrinology, Kayseri, TurkeyORCID 0000-0002-2100-3628
Mikail DemirErciyes University Faculty of Medicine, Department of Medical Genetics, Kayseri, TurkeyORCID 0000-0001-8411-5179
Munis DündarErciyes University Faculty of Medicine, Department of Medical Genetics, Kayseri, TurkeyORCID 0000-0003-0969-4611

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Neonatal diabetes and congenital hypothyroidism (CH) syndrome is a rare condition caused by homozygous or compound heterozygous mutations in the

Indexed as

Bone Diseases, MetabolicCongenital HypothyroidismDeafnessDiabetes MellitusGlaucomaInfant, Newborn, DiseasesDNA-Binding ProteinsHumansInfant, NewbornMaleMutationRepressor ProteinsSyndromeTrans-ActivatorsTranscription FactorsDNA-Binding ProteinsGLIS3 protein, humanRepressor ProteinsTrans-ActivatorsTranscription Factorscongenital glaucomacongenital hypothyroidismGLIS3neonatal diabetes

Identifiers

PMID35410112
PMCPMC10683540

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.