ReviewEndocrinology and metabolism clinics of North America2017
Defects of Thyroid Hormone Synthesis and Action.
Review in Endocrinology and metabolism clinics of North America, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.
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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.
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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.
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Who cites it
10 citing papers in PubMed, 37 citations in OpenAlex.
- Interesting neuroimaging findings in a child with hyperlipidemia: a case report.BMC pediatrics · 2026Article
- New insights into the hypothalamic-pituitary-thyroid axis: a transcriptome- and proteome-wide association study.European thyroid journal · 2024Article
- Effects of the Sex Factor on Mouse Iodine Intake: Interactions between the Gut Microbiota Composition and Metabolic Syndromes.ACS omega · 2021Article
- Analysis of Mutation Spectra of 28 Pathogenic Genes Associated With Congenital Hypothyroidism in the Chinese Han Population.Frontiers in endocrinology · 2021Article
- Article
- Congenital hypothyroidism due to thyroglobulin deficiency: a case report with a novel mutation in TG gene.Annals of pediatric endocrinology & metabolism · 2019Article
- Implications of NaJournal of the Endocrine Society · 2019Review
- Clinical genetics of defects in thyroid hormone synthesis.Annals of pediatric endocrinology & metabolism · 2018Article
- Mutation screening in the genes PAX-8, NKX2-5, TSH-R, HES-1 in cohort of 63 Brazilian children with thyroid dysgenesis.Archives of endocrinology and metabolism · 2018Article
- A novel mutation in the TG gene (G2322S) causing congenital hypothyroidism in a Sudanese family: a case report.BMC medical genetics · 2018Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
2 authors at 1 institution in 1 country.
Funding
Abstract
Congenital hypothyroidism (CH) is the most common inborn endocrine disorder and causes significant morbidity. To date, we are only aware of the molecular basis responsible for the defects in a small portion of patients with CH. A better understanding of the pathophysiology of these cases at the genetic and molecular basis provides useful information for proper counseling to patients and their families a well as for the development of better targeted therapies. This article provides a succinct outline of the pathophysiology and genetics of the known causes of thyroid dysgenesis, dyshormonogenesis, and syndrome of impaired sensitivity to thyroid hormone.
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Registered trials
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.