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

Steroid disorders in children: congenital adrenal hyperplasia and apparent mineralocorticoid excess.

Proceedings of the National Academy of Sciences of the United States of America - 26 Oct 1999

New M I, Wilson R C

Abstract excerpt

Our research team and laboratories have concentrated on two inherited endocrine disorders, congenital adrenal hyperplasia (CAH) and apparent mineralocorticoid excess, in thier investigations of the pathophysiology of adrenal steroid hormone disorders in children. CAH refers to a family of inherited disorders in which defects occur in one of the enzymatic steps required to synthesize cortisol from cholesterol in...

Read the complete abstract on PubMed

Topics

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

Share to Adrenal Hyperplasia, Congenital
Share to Cytochrome P-450 Enzyme System

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Dexamethasone

Share to Infant, Newborn

Share to Mineralocorticoids

Share to Neonatal Screening

Share to Prenatal Diagnosis

Share to Steroid 21-Hydroxylase

Source

Open in PubMed Open full text

Identifiers

PMID: 10536001
DOI: 10.1073/pnas.96.22.12790
PMCID: PMC23101

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Steroid disorders in children: congenital adrenal hyperplasia and apparent mineralocorticoid excess.PMID 10536001Read ↗

An update of congenital adrenal hyperplasia.Semantic proximity Read ↗

Congenital Adrenal Hyperplasia-Current Insights in Pathophysiology, Diagnostics, and Management.Semantic proximity Read ↗

Congenital adrenal hyperplasia.Semantic proximity Read ↗

Congenital adrenal hyperplasias.Semantic proximity Read ↗

Congenital adrenal hyperplasia: biochemical and molecular perspectives.Semantic proximity Read ↗

Congenital adrenal hyperplasia due to 21 hydroxylase deficiency: from birth to adulthood.Semantic proximity Read ↗

Update on diagnosis and management of congenital adrenal hyperplasia due to 21-hydroxylase deficiencySemantic proximity Read ↗

Clinical and molecular review of atypical congenital adrenal hyperplasiaSemantic proximity Read ↗

Diagnosis and management of classical congenital adrenal hyperplasia.Semantic proximity Read ↗

Steroid 21-hydroxylase deficiency in congenital adrenal hyperplasia.Semantic proximity Read ↗

Congenital adrenal hyperplasia: update on prenatal diagnosis and treatment.Semantic proximity Read ↗

Congenital adrenal hyperplasia. Molecular insights learned from patients.Semantic proximity Read ↗

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