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

Familial persistent hyperinsulinemic hypoglycemia of infancy and mutations in the sulfonylurea receptor.

The New England journal of medicine - 6 Mar 1997

Dunne M J, Kane C, Shepherd R M, Sanchez J A, James R F, Johnson P R, Aynsley-Green A, Lu S, Clement J P, Lindley K J, Seino S, Aguilar-Bryan L

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 Hyperinsulinism
Share to Hypoglycemia
Share to Insulin Secretion
Share to Islets of Langerhans

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Potassium Channels, Inwardly Rectifying

Share to Receptors, Drug

Share to Sulfonylurea Compounds

Share to Sulfonylurea Receptors

Source

Identifiers

PMID: 9041101
DOI: 10.1056/NEJM199703063361005

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Familial persistent hyperinsulinemic hypoglycemia of infancy and mutations in the sulfonylurea receptor.PMID 9041101Read ↗

Further evidence for a dominant form of familial persistent hyperinsulinemic hypoglycemia of infancy: a family with documented hyperinsulinemia in two generations.Semantic proximity Read ↗

Hyperinsulinemic hypoglycemia of infancy. Recent insights into ATP-sensitive potassium channels, sulfonylurea receptors, molecular mechanisms, and treatment.Semantic proximity Read ↗

Congenital hyperinsulinism disorders: Genetic and clinical characteristicsSemantic proximity Read ↗

The molecular basis of persistent hyperinsulinemic hypoglycemia of infancy and its pathologic substrates.Semantic proximity Read ↗

Genetics of congenital hyperinsulinemic hypoglycemia.Semantic proximity Read ↗

Familial hyperinsulinism and pancreatic beta-cell ATP-sensitive potassium channels.Semantic proximity Read ↗

An autosomal dominant form of familial persistent hyperinsulinemic hypoglycemia of infancy, not linked to the sulfonylurea receptor locus.Semantic proximity Read ↗

Clinical and genetic heterogeneity in congenital hyperinsulinism.Semantic proximity Read ↗

Novel de novo mutation in sulfonylurea receptor 1 presenting as hyperinsulinism in infancy followed by overt diabetes in early adolescence.Semantic proximity Read ↗

Congenital Hyperinsulinism.Semantic proximity Read ↗

Persistent hyperinsulinemic hypoglycemia of infancy due to homozygous KCNJ11 (T294M) mutation.Semantic proximity Read ↗

Hyperinsulinism of infancy: novel ABCC8 and KCNJ11 mutations and evidence for additional locus heterogeneity.Semantic proximity Read ↗

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