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 three patients from the same family. Expanding the genotype of this disease.

Anales de pediatria - 1 Aug 2021

Herrera Azabache Katia, Muñoz Bermúdez Zoraya, Ferrández Mengual David, Nso-Roca Ana Pilar

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 Congenital Hyperinsulinism
Share to Genotype

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 34373074
DOI: 10.1016/j.anpede.2020.07.017

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 · 12 closest

Congenital hyperinsulinism in three patients from the same family. Expanding the genotype of this disease.PMID 34373074Read ↗

A little bit of everything: molecular genetics of congenital hyperinsulinism.Semantic proximity Read ↗

Genetics of congenital hyperinsulinemic hypoglycemia.Semantic proximity Read ↗

Congenital hyperinsulinism disorders: Genetic and clinical characteristicsSemantic proximity Read ↗

Molecular genetics and phenotype of 26 Vietnamese patients with congenital hyperinsulinismSemantic proximity Read ↗

Congenital hyperinsulinism presenting with different clinical, biochemical and molecular genetic spectra.Semantic proximity Read ↗

Genetics of congenital hyperinsulinism.Semantic proximity Read ↗

Congenital hyperinsulinism.Semantic proximity Read ↗

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

Molecular genetics, correlation between genotype and phenotype of 65 Vietnames patients with congenital hyperinsulinismSemantic proximity Read ↗

Comprehensive clinical and molecular characterization with long-term outcomes in 40 patients with congenital hyperinsulinismSemantic proximity Read ↗

Genetics of neonatal hyperinsulinism.Semantic proximity Read ↗

Familial hyperinsulinism caused by an activating glucokinase mutation.Semantic proximity Read ↗

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