Evidence map›Paper›PMID 34093443›Full record

ArticleFrontiers in endocrinology2021

Case Report: Neonatal Diabetes Mellitus Caused by a Novel

Shira London, Elisa De Franco, Ghadir Elias-Assad, Marie Noufi Barhoum, Clari Felszer, Marina Paniakov, Scott A Weiner, Yardena Tenenbaum-Rakover

Open access · goldAbstract readCase Reports
In one paragraph

Article in Frontiers in endocrinology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

15 citing papers in PubMed, 19 citations in OpenAlex.

  1. A Novel Renal Manifestation inJournal of medical cases · 2026
    Article
  2. Glis3 Is a Modifier of Cyst Progression in Autosomal Dominant Polycystic Kidney Disease.Journal of the American Society of Nephrology : JASN · 2026
    Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Insulin Delivery Technology for Treatment of Infants with Neonatal Diabetes Mellitus: A Systematic Review.Diabetes therapy : research, treatment and education of diabetes and related disorders · 2024
    Review
  9. Article
  10. Article
  11. Neonatal Diabetes, Congenital Hypothyroidism, and Congenital Glaucoma Coexistence: A Case ofJournal of clinical research in pediatric endocrinology · 2023
    Article
  12. Article
  13. Article
  14. Review
  15. 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

8 authors at 3 institutions in 2 countries.

Shira LondonPediatric Endocrine Institute, Ha'Emek Medical Center, Afula, Israel.
Elisa De FrancoInstitute of Biomedical and Clinical Science, College of Medicine and Health, University of Exeter, Exeter, United Kingdom.
Ghadir Elias-AssadPediatric Endocrine Institute, Ha'Emek Medical Center, Afula, Israel.
Marie Noufi BarhoumPediatric Endocrine Institute, Ha'Emek Medical Center, Afula, Israel.
Clari FelszerNeonatal Intensive Care Unit, Ha'Emek Medical Center, Afula, Israel.
Marina PaniakovNeonatal Intensive Care Unit, Ha'Emek Medical Center, Afula, Israel.
Scott A WeinerNeonatal Intensive Care Unit, Ha'Emek Medical Center, Afula, Israel.
Yardena Tenenbaum-RakoverPediatric Endocrine Institute, Ha'Emek Medical Center, Afula, Israel.
Emek Medical Center · ILBar-Ilan University · ILUniversity of Exeter · GB

Funding

Wellcome Trust
6 · The paper itself

Abstract

Background: Mutations in Cases: We describe non-identical twins born to consanguineous parents presenting with NDM, congenital hypothyroidism, congenital glaucoma, hepatic cholestasis, cystic kidney and delayed psychomotor development. Sequence analysis of Conclusions: This report highlights the importance of early molecular diagnosis for appropriate management of NDM. We describe a novel nonsense mutation of

Indexed as

MutationBiomarkersBlood GlucoseChild, PreschoolCongenital HypothyroidismDiabetes MellitusDNA-Binding ProteinsFemaleGene Expression RegulationHumansInfant, NewbornInfant, Newborn, DiseasesMalePhenotypePrognosisRepressor ProteinsBiomarkersBlood GlucoseDNA-Binding ProteinsGLIS3 protein, humanRepressor ProteinsTrans-Activatorscongenital glaucomacongenital hypothyroidismGLIS3 mutationneonatal diabetesβ-cell development

Identifiers

PMID34093443
PMCPMC8169976
OpenAlexW3162566132

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.