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

Precision medicine in KCNJ11 permanent neonatal diabetes.

The lancet. Diabetes & endocrinology - 1 Aug 2018

Greeley Siri Atma W, Letourneau Lisa R, Philipson Louis H

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 Cohort Studies
Share to Diabetes Mellitus
Share to KCNJ11 gene
Share to Mutation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Precision Medicine

Source

Open in PubMed Open full text

Identifiers

PMID: 29880307
DOI: 10.1016/S2213-8587(18)30138-4
PMCID: PMC6345272

Genes

KCNJ11

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Precision medicine in KCNJ11 permanent neonatal diabetes.PMID 29880307Read ↗

Personalized precision medicine in extreme preterm infants with transient neonatal diabetes mellitus.Semantic proximity Read ↗

Genetics and neonatal diabetes: towards precision medicine.Semantic proximity Read ↗

KCNJ11 activating mutations are associated with developmental delay, epilepsy and neonatal diabetes syndrome and other neurological featuresSemantic proximity Read ↗

Monogenic diabetes: a gateway to precision medicine in diabetes.Semantic proximity Read ↗

Utilizing the KCNJ11 Gene Mutations in Spotting Egyptian Patients With Permanent Neonatal Diabetes Who Can Benefit From Treatment Shift.Semantic proximity Read ↗

Precision Medicine and Rare Genetic Variants.Semantic proximity Read ↗

From diagnostic testing to precision medicine: the evolving role of genomics in cardiac channelopathies and cardiomyopathies in childrenSemantic proximity Read ↗

Atypical cerebral palsy: genomics analysis enables precision medicineSemantic proximity Read ↗

YIPF5 mutations cause neonatal diabetes and microcephaly: progress for precision medicine and mechanistic understanding.Semantic proximity Read ↗

Fresh insight into neonatal diabetes mutations.Semantic proximity Read ↗

Role of Actionable Genes in Pursuing a True Approach of Precision Medicine in Monogenic Diabetes.Semantic proximity Read ↗

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

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