Mitotane for 21-hydroxylase deficiency in an infertile man.

doi:10.1056/NEJMc1410041

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

Community

Back to search

Article

Mitotane for 21-hydroxylase deficiency in an infertile man.

The New England journal of medicine - 20 Nov 2014

Bry-Gauillard Hélène, Cartes Alejandra, Young Jacques

Abstract excerpt

No abstract is available from the source.

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 Antineoplastic Agents, Hormonal
Share to Azoospermia
Share to Gonadotropins

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Hormones

Share to Steroid 21-Hydroxylase

Share to Testicular Neoplasms

Share to Testis

Source

Open in PubMed

Identifiers

PMID: 25409392
DOI: 10.1056/NEJMc1410041

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 8 closest

Mitotane for 21-hydroxylase deficiency in an infertile man.PMID 25409392Read ↗

[Current data on the molecular biology of 21-hydroxylase deficiency. Diagnostic applications].Semantic proximity Read ↗

Psychosis in a male pseudohermaphrodite with 17-hydroxylase deficiency.Semantic proximity Read ↗

An overview of molecular diagnosis of steroid 21-hydroxylase deficiency.Semantic proximity Read ↗

Two brothers with non-classical 21-hydroxylase deficiency: to treat or not to treat?Semantic proximity Read ↗

[21-Hydroxylase deficiency (nonclassical type)].Semantic proximity Read ↗

[21-Hydroxylase deficiency (classical type)].Semantic proximity Read ↗

Functional consequences of a novel point mutation in the CYP21A2 gene identified in a Chinese Han patient with nonclassic 21-hydroxylase deficiency.Semantic proximity Read ↗

[11Beta-hydroxylase deficiency].Semantic proximity Read ↗

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