Article

Neonatal diabetes as an isolated manifestation of ipex: an expanding spectrum of disease phenotype with FOXP3 mutation

2015-01-01

Abstract excerpt

No abstract is available from the source.

Topics

Open a Topic to create a Post that cites this publication.

Identifiers and source

Literature Corpus work: 40d2933d-c01f-59b6-9330-ec2c3e7b57e2
DOI: 10.1186/1687-9856-2015-s1-p11
PMCID: PMC4429078

Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest

Neonatal diabetes as an isolated manifestation of ipex: an expanding spectrum of disease phenotype with FOXP3 mutationDOI 10.1186/1687-9856-2015-s1-p11Read

A Case Report of IPEX Syndrome with Neonatal Diabetes Mellitus and Congenital Hypothyroidism as the Initial Presentation, and a Systematic Review of neonatal IPEX.Semantic proximity Read

Congenital Diabetes: Comprehensive Genetic Testing Allows for Improved Diagnosis and Treatment of Diabetes and Other Associated Features.Semantic proximity Read

Clinical heterogeneity in patients with FOXP3 mutations presenting with permanent neonatal diabetes.Semantic proximity Read

FOXP3 mutations causing early‐onset insulin‐requiring diabetes but without other features of immune dysregulation, polyendocrinopathy, enteropathy, X‐linked syndromeSemantic proximity Read

Wolcott-Rallison syndrome: pathogenic insights into neonatal diabetes from new mutation and expression studies of EIF2AK3.Semantic proximity Read

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

Neonatal diabetes mellitus around the world: Update 2024.Semantic proximity Read

Update in neonatal diabetes.Semantic proximity Read

Entities and frequency of neonatal diabetes: data from the diabetes documentation and quality management system (DPV).Semantic proximity Read

Infantile presentation of MODY 3 diabetes.Semantic proximity Read

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

Genetic and clinical heterogeneity of permanent neonatal diabetes mellitus: a single tertiary centre experience.Semantic proximity Read