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

Clinical and molecular genetics of neonatal diabetes due to mutations in the insulin gene.

Reviews in endocrine & metabolic disorders - 1 Sept 2010

Støy Julie, Steiner Donald F, Park Soo-Young, Ye Honggang, Philipson Louis H, Bell Graeme I

Abstract excerpt

Over the last decade our insight into the causes of neonatal diabetes has greatly expanded. Neonatal diabetes was once considered a variant of type 1 diabetes that presented early in life. Recent advances in our understanding of this disorder have established that neonatal diabetes is not an auto...

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 Diabetes Mellitus, Type 1
Share to Infant, Newborn

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Infant, Newborn, Diseases

Share to Insulin

Share to Models, Biological

Share to Molecular Biology

Share to Proinsulin

Source

Open in PubMed Open full text

Identifiers

PMID: 20938745
DOI: 10.1007/s11154-010-9151-3
PMCID: PMC2974937

Genes

INS
ABCC8
KCNJ11

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-20938745-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Clinical and molecular genetics of neonatal diabetes due to mutations in the insulin gene.PMID 20938745Read ↗

Neonatal diabetes: an expanding list of genes allows for improved diagnosis and treatment.Semantic proximity Read ↗

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

Emerging technologies in pediatrics: the paradigm of neonatal diabetes mellitus.Semantic proximity Read ↗

[Neonatal diabetes mellitus].Semantic proximity Read ↗

Permanent neonatal diabetes mellitus--the importance of diabetes differential diagnosis in neonates and infants.Semantic proximity Read ↗

Update in neonatal diabetes.Semantic proximity Read ↗

Neonatal Diabetes Mellitus: An Update on Diagnosis and Management.Semantic proximity Read ↗

Diabetes mellitus in neonates and infants: genetic heterogeneity, clinical approach to diagnosis, and therapeutic options.Semantic proximity Read ↗

Identification of insulin gene variants in neonatal diabetes.Semantic proximity Read ↗

In celebration of a century with insulin - Update of insulin gene mutations in diabetes.Semantic proximity Read ↗

[Neonatal diabetes mellitus].Semantic proximity Read ↗

Heterozygous missense mutations in the insulin gene are linked to permanent diabetes appearing in the neonatal period or in early infancy: a report from the French ND (Neonatal Diabetes) Study Group.Semantic proximity Read ↗

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