Evidence map›Paper›PMID 39126042›Full record

ArticleInternational journal of molecular sciences2024

Patients with Thyroid Dyshormonogenesis and

Noelia Baz-Redón, María Antolín, María Clemente, Ariadna Campos, Eduard Mogas, Mónica Fernández-Cancio, Elisenda Zafon, Elena García-Arumí, Laura Soler, Núria González-Llorens and 3 more

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Review
  5. 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

13 authors.

Noelia Baz-RedónGrowth and Development Group, Vall d'Hebron Research Institute (VHIR), Hospital Universitari Vall d'Hebron, 08035 Barcelona, Spain.ORCID 0000-0003-1704-3413
María AntolínDepartment of Clinical and Molecular Genetics and Rare Disease, Hospital Universitari Vall d'Hebron, 08035 Barcelona, Spain.
María ClementeGrowth and Development Group, Vall d'Hebron Research Institute (VHIR), Hospital Universitari Vall d'Hebron, 08035 Barcelona, Spain.
Ariadna CamposGrowth and Development Group, Vall d'Hebron Research Institute (VHIR), Hospital Universitari Vall d'Hebron, 08035 Barcelona, Spain.
Eduard MogasGrowth and Development Group, Vall d'Hebron Research Institute (VHIR), Hospital Universitari Vall d'Hebron, 08035 Barcelona, Spain.ORCID 0000-0001-8501-5364
Mónica Fernández-CancioGrowth and Development Group, Vall d'Hebron Research Institute (VHIR), Hospital Universitari Vall d'Hebron, 08035 Barcelona, Spain.
Elisenda ZafonDepartment of Clinical and Molecular Genetics and Rare Disease, Hospital Universitari Vall d'Hebron, 08035 Barcelona, Spain.
Elena García-ArumíCentro de Investigación Biomédica en Red de Enfermedades Raras (CIBERER), Instituto de Salud Carlos III, 28029 Madrid, Spain.
Laura SolerPediatric Endocrinology Section, Hospital Universitari Vall d'Hebron, 08035 Barcelona, Spain.
Núria González-LlorensPediatric Endocrinology Section, Hospital Universitari Vall d'Hebron, 08035 Barcelona, Spain.ORCID 0000-0003-0550-4665
Cristina Aguilar-RieraPediatric Endocrinology Section, Hospital Universitari Vall d'Hebron, 08035 Barcelona, Spain.ORCID 0000-0001-5256-3743
Núria Camats-TarruellaGrowth and Development Group, Vall d'Hebron Research Institute (VHIR), Hospital Universitari Vall d'Hebron, 08035 Barcelona, Spain.ORCID 0000-0002-4863-8201
Diego YesteGrowth and Development Group, Vall d'Hebron Research Institute (VHIR), Hospital Universitari Vall d'Hebron, 08035 Barcelona, Spain.ORCID 0000-0002-6620-6525

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Thyroid dyshormonogenesis (THD) is a heterogeneous group of genetic diseases caused by the total or partial defect in the synthesis or secretion of thyroid hormones. Genetic variants in

Indexed as

Dual OxidasesGenetic Association StudiesCongenital HypothyroidismFemaleGenotypeHumansInfant, NewbornMaleMutationNeonatal ScreeningPhenotypeThyroid DysgenesisThyroxineDual OxidasesDUOX2 protein, humanThyroxineCHcongenital hypothyroidismdual oxidase 2DUOX2phenotypic variabilitythyroid dyshormonogenesis

Identifiers

PMID39126042
PMCPMC11313534

What OpenQuestion holds

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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.