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

Molecular and clinical features of KATP -channel neonatal diabetes mellitus in Japan.

Pediatric diabetes - 1 Nov 2017

Hashimoto Yukiko, Dateki Sumito, Hirose Masakazu, Satomura Kenichi, Sawada Hirotake, Mizuno Haruo, Sugihara Shigetaka, Maruyama Koichi, Urakami Tatsuhiko, Sugawara Hidenori, Shirai Kenji, Yorifuji Tohru

Abstract excerpt

BACKGROUND: There are few reports pertaining to Asian patients with neonatal diabetes mellitus (NDM) caused by activating mutations in the ATP-sensitive potassium channel genes (KATP-NDM). OBJECTIVES: To elucidate the characteristics of Japanese patients with KATP-NDM. METHODS: By the amplification and direct sequencing of all exons and exon-intron boundaries of the KCNJ11 and ABCC8 genes, 25 patients with...

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 Drug Monitoring

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Glyburide

Share to Hyperglycemia

Share to Hypoglycemia

Share to Infant, Newborn, Diseases

Share to Psychomotor Disorders

Share to Sulfonylurea Receptors

Source

Identifiers

PMID: 27681997
DOI: 10.1111/pedi.12447

Genes

ABCC8
KCNJ11

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Molecular and clinical features of KATP -channel neonatal diabetes mellitus in Japan.PMID 27681997Read ↗

Genotype-phenotype correlation of KATP channel gene defects causing permanent neonatal diabetes in Indian patients.Semantic proximity Read ↗

Clinical and Genetic Characteristics of ABCC8 Nonneonatal Diabetes Mellitus: A Systematic Review.Semantic proximity Read ↗

DEND Syndrome with Heterozygous KCNJ11 Mutation Successfully Treated with Sulfonylurea.Semantic proximity Read ↗

KATP Channel Mutations and Neonatal Diabetes.Semantic proximity Read ↗

Clinical characteristics and molecular genetic analysis of 22 patients with neonatal diabetes from the South-Eastern region of Turkey: predominance of non-KATP channel mutations.Semantic proximity Read ↗

Genetic Analysis and Follow-Up of 25 Neonatal Diabetes Mellitus Patients in China.Semantic proximity Read ↗

Clinical and molecular characterization of neonatal diabetes and monogenic syndromic diabetes in Asian Indian children.Semantic proximity Read ↗

A novel mutation causing DEND syndrome: a treatable channelopathy of pancreas and brain.Semantic proximity Read ↗

Epidemiology, clinical characteristics, and genetic etiology of neonatal diabetes in Japan.Semantic proximity Read ↗

Clinical features and partial proportional molecular genetics in neonatal diabetes mellitus: a retrospective analysis in southwestern China.Semantic proximity Read ↗

Characterization of ABCC8 and KCNJ11 gene mutations and phenotypes in Korean patients with congenital hyperinsulinism.Semantic proximity Read ↗

Clinical and Molecular Characterization of Children with Neonatal Diabetes Mellitus at a Tertiary Care Center in Northern India.Semantic proximity Read ↗

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