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

[Congenital hyperinsulinism in the north-east Netherlands. Clinical features and DNA diagnostics in 22 children].

Nederlands tijdschrift voor geneeskunde - 1 Jan 2011

Verheul Jorieke C, Ris-Stalpers Carrie, Bikker Hennie, Bakker-van Waarde Willie M, Noordam Cees

Abstract excerpt

OBJECTIVE: To describe the clinical features and relevant genetic mutations in 22 children with congenital hyperinsulinism in the north-east Netherlands. DESIGN: Retrospective, descriptive study. METHOD: Children born between June 1988 and June 2009, who were presented at the academic medical centres of Nijmegen and Groningen were included. They were clinically suspected of having congenital hyperinsulinism and...

Read the complete abstract on PubMed

Topics

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

Share to ATP-Binding Cassette Transporters
Share to Congenital Hyperinsulinism

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Diazoxide

Share to DNA Mutational Analysis

Share to Infant, Newborn

Share to Pancreatectomy

Share to Pedigree

Share to Potassium Channels, Inwardly Rectifying

Source

Identifiers

PMID: 21835061

Genes

ABCC8
GCK
GLUD1
KCNJ11

Variants

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.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Congenital hyperinsulinism in the north-east Netherlands. Clinical features and DNA diagnostics in 22 children].PMID 21835061Read ↗

Investigating Genetic Mutations in a Large Cohort of Iranian Patients with Congenital HyperinsulinismSemantic proximity Read ↗

[Clinical features and genetic analysis of seven patients with congenital hyperinsulinism].Semantic proximity Read ↗

Clinical characteristics and phenotype-genotype analysis in Turkish patients with congenital hyperinsulinism; predominance of recessive KATP channel mutations.Semantic proximity Read ↗

Clinical and molecular characterisation of 300 patients with congenital hyperinsulinism.Semantic proximity Read ↗

Genetic and Clinical Characterisation of Congenital Hyperinsulinism: Identification of a Novel ABCC8 Variant.Semantic proximity Read ↗

Characterization of the ABCC8 gene mutation and phenotype in patients with congenital hyperinsulinism in western Saudi Arabia.Semantic proximity Read ↗

[Congenital hyperinsulinism--new causes and clinical variations].Semantic proximity Read ↗

Clinical and genetic characterization of congenital hyperinsulinism in Spain.Semantic proximity Read ↗

Clinical and genetic evaluation of patients with KATP channel mutations from the German registry for congenital hyperinsulinism.Semantic proximity Read ↗

Congenital hyperinsulinism in Chinese patients: 5-yr treatment outcome of 95 clinical cases with genetic analysis of 55 cases.Semantic proximity Read ↗

[Analysis of genetic variants in four children with congenital hyperinsulinemia].Semantic proximity Read ↗

Current Status of Childhood Hyperinsulinemic Hypoglycemia in Turkey.Semantic proximity Read ↗

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