Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Alterations of neonatal thyroid function.

Acta paediatrica (Oslo, Norway : 1992). Supplement - 1 Feb 1999

Grüters A, Krude H, Biebermann H, Liesenkötter K P, Schöneberg T, Gudermann T

Abstract excerpt

Recent progress has been made in understanding the pathogenesis of neonatal thyroid disorders. Autosomal recessive inheritance of mutations of the thyroid peroxidase and thyroglobulin genes has been described in some patients with congenital hypothyroidism (CH) and a family history of CH. Autosom...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Hyperthyroidism
Share to Hypothyroidism
Share to Mass Screening

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Primary Prevention

Share to Thyroid Function Tests

Share to Thyroid Gland

Share to Thyrotropin

Share to Congenital Hypothyroidism

Source

Identifiers

PMID: 10102047
DOI: 10.1111/j.1651-2227.1999.tb14346.x

Genes

PAX8

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-10102047-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Alterations of neonatal thyroid function.PMID 10102047Read ↗

Neonatal thyroid disorders.Semantic proximity Read ↗

Molecular pathogenesis of neonatal hypothyroidism.Semantic proximity Read ↗

Thyroglobulin gene mutations and other genetic defects associated with congenital hypothyroidism.Semantic proximity Read ↗

Hyperthyroidism in early infancy: pathogenesis, clinical features and diagnosis with a focus on neonatal hyperthyroidism.Semantic proximity Read ↗

Genetics of congenital hypothyroidism.Semantic proximity Read ↗

Prevalence and course of thyroid dysfunction in neonates at high risk of Graves' disease or with non-autoimmune hyperthyroidism.Semantic proximity Read ↗

Extreme phenotypic variability of thyroid dysgenesis in six new cases of congenital hypothyroidism due to PAX8 gene loss-of-function mutations.Semantic proximity Read ↗

Heterogeneous phenotype in children affected by non-autoimmune hypothyroidism: an update.Semantic proximity Read ↗

Genetics of congenital hypothyroidism: Modern conceptsSemantic proximity Read ↗

Update on Neonatal Isolated Hyperthyrotropinemia: A Systematic Review.Semantic proximity Read ↗

Extrathyroidal congenital defects in children with congenital hypothyroidism - observations from a single paediatric centre in Central Europe with a review of literature.Semantic proximity Read ↗

[Genetic of congenital hypothyroidism].Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.