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Article

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

The Journal of clinical endocrinology and metabolism - 1 Jun 1998

Hufnagel M, Eichmann D, Stieh J, Santer R

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Share to ATP-Binding Cassette Transporters
Share to Hyperinsulinism
Share to Hypoglycemia
Share to Infant

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

Share to Potassium Channels

Share to Potassium Channels, Inwardly Rectifying

Share to Receptors, Drug

Share to Sulfonylurea Receptors

Source

Identifiers

PMID: 9626165
DOI: 10.1210/jc.83.6.2215-a

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

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Research trail→

Click a neighbor to travelStep 1 · 12 closest

Further evidence for a dominant form of familial persistent hyperinsulinemic hypoglycemia of infancy: a family with documented hyperinsulinemia in two generations.PMID 9626165Read ↗

Familial persistent hyperinsulinemic hypoglycemia of infancy and mutations in the sulfonylurea receptor.Semantic proximity Read ↗

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

[Persistent hyperinsulinemic hypoglycemia of infancy (PHHI)].Semantic proximity Read ↗

Hyperinsulinism in infancy: understanding the pathophysiology.Semantic proximity Read ↗

Congenital hyperinsulinism disorders: Genetic and clinical characteristicsSemantic proximity Read ↗

Congenital hyperinsulinism in three patients from the same family. Expanding the genotype of this disease.Semantic proximity Read ↗

Persistent hyperinsulinemic hypoglycemia of infancy.Semantic proximity Read ↗

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

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

Increased plasma incretin concentrations identifies a subset of patients with persistent congenital hyperinsulinism without KATP channel gene defects.Semantic proximity Read ↗

[PHHI (persistent hyperinsulinemic hypoglycemia of infancy)].Semantic proximity Read ↗

Genetic mutations as a cause of hyperinsulinemic hypoglycemia in children.Semantic proximity Read ↗

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