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

Nephrogenic diabetes insipidus.

The American journal of medicine - 1 Nov 1998

Bichet D G

Abstract excerpt

In nephrogenic diabetes insipidus, the kidney is unable to concentrate urine despite normal or elevated concentrations of the antidiuretic hormone arginine vasopressin (AVP). In congenital nephrogenic diabetes insipidus (NDI), the obvious clinical manifestations of the disease, that is polyuria and polydipsia, are present at birth and need to be immediately recognized to avoid severe episodes of dehydration. Most...

Read the complete abstract on PubMed

Topics

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

Share to Aquaporins
Share to Diabetes Insipidus, Nephrogenic
Share to AVP gene

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

Share to GTP-Binding Proteins

Share to Mutation

Share to Protein Binding

Share to Protein Structure, Tertiary

Share to Receptors, Vasopressin

Source

Identifiers

PMID: 9831428
DOI: 10.1016/s0002-9343(98)00301-5

Genes

AQP2
AVP
AVPR2

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

Nephrogenic diabetes insipidus.PMID 9831428Read ↗

Nephrogenic diabetes insipidus.Semantic proximity Read ↗

Nephrogenic diabetes insipidus.Semantic proximity Read ↗

Genetic forms of nephrogenic diabetes insipidus (NDI): Vasopressin receptor defect (X-linked) and aquaporin defect (autosomal recessive and dominant).Semantic proximity Read ↗

V2R mutations and nephrogenic diabetes insipidus.Semantic proximity Read ↗

Genetic basis of nephrogenic diabetes insipidus.Semantic proximity Read ↗

Physiopathology and diagnosis of nephrogenic diabetes insipidus.Semantic proximity Read ↗

Hereditary Nephrogenic Diabetes Insipidus: Pathophysiology and Possible Treatment. An Update.Semantic proximity Read ↗

GENETICS IN ENDOCRINOLOGY Pathophysiology, diagnosis and treatment of familial nephrogenic diabetes insipidus.Semantic proximity Read ↗

[Nephrogenic diabetes insipidus].Semantic proximity Read ↗

Congenital nephrogenic diabetes insipidus: the current state of affairs.Semantic proximity Read ↗

Nephrogenic diabetes insipidus: essential insights into the molecular background and potential therapies for treatment.Semantic proximity Read ↗

Vasopressin receptor mutations causing nephrogenic diabetes insipidus.Semantic proximity Read ↗

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