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

Analysis of clinical and genetic characteristics of Chinese children with congenital hyperinsulinemia that is spontaneously relieved.

Endocrine - 1 Apr 2021

Xu Zi-di, Hui Pei-Pei, Zhang Wei, Zeng Qiao, Zhang Lin, Liu Min, Yan Jie, Wu Yu-Jun, Sang Yan-Mei

Abstract excerpt

OBJECTIVE: This study aimed to analyze the clinical and genetic characteristics of Chinese children with congenital hyperinsulinemia (CHI) that is spontaneously relieved. METHODS: The patient group comprised 200 children with CHI that were treated at the Beijing Children's Hospital from January 2006 to December 2018. The patients were divided into two groups according to their prognosis: the spontaneous remission...

Read the complete abstract on PubMed

Topics

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

Share to Child
Share to China
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

Share to Mutation

Source

Open in PubMed Open full text

Identifiers

PMID: 33502730
DOI: 10.1007/s12020-020-02585-x
PMCID: PMC8087546

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

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

Analysis of clinical and genetic characteristics of Chinese children with congenital hyperinsulinemia that is spontaneously relieved.PMID 33502730Read ↗

Diagnosis and treatment of a newborn with congenital hyperinsulinemia:Case report and literature reviewSemantic proximity Read ↗

Congenital hyperinsulinism in infancy and childhood: challenges, unmet needs and the perspective of patients and familiesSemantic proximity Read ↗

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

Genetic characteristics and long-term follow-up of 11 patients with congenital hyperinsulinism followed in a single center.Semantic proximity Read ↗

Evaluation and management of neonatal onset hyperinsulinemic hypoglycemia: a single neonatal center experience.Semantic proximity Read ↗

Molecular Characterization and Management of Congenital Hyperinsulinism: A Tertiary Centre Experience.Semantic proximity Read ↗

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

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

Diagnosis, treatment and genetic analysis of two cases of congenital hyperinsulinemic hypoglycemia caused by GCK gene mutation.Semantic proximity Read ↗

Congenital hyperinsulinism: current trends in diagnosis and therapySemantic proximity Read ↗

Congenital hyperinsulinism: recent updates on molecular mechanisms, diagnosis and management.Semantic proximity Read ↗

Clinical and genetic characteristics of patients with congenital hyperinsulinism in 21 non-consanguineous families from Serbia.Semantic proximity Read ↗

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