Permanent neonatal diabetes mellitus: prevalence and genetic diagnosis in the SEARCH for Diabetes in Youth Study (Q33912545)

30 July 2017

Permanent neonatal diabetes mellitus: prevalence and genetic diagnosis in the SEARCH for Diabetes in Youth Study (English)

1 reference

permanent neonatal diabetes mellitus

30 July 2017

1 reference

inferred from title

author

Andrew Tym Hattersley

10

SEARCH for Diabetes in Youth Study Group

Andrew Hattersley

0 references

13

SEARCH for Diabetes in Youth Study Group

1 reference

30 July 2017

6

Dana Dabelea

1 reference

30 July 2017

Giuseppina Imperatore

9

Giuseppina Imperatore

1 reference

30 July 2017

Sian Ellard

11

0 references

Catherine Pihoker

2

Catherine Pihoker

1 reference

30 July 2017

7

Beatriz Rodriguez

1 reference

30 July 2017

12

Lisa K Gilliam

1 reference

30 July 2017

3

Lawrence M Dolan

1 reference

30 July 2017

Roopa Kanakatti Shankar

1

1 reference

30 July 2017

Debra Standiford

4

1 reference

30 July 2017

Angela Badaru

5

1 reference

30 July 2017

Mary Helen Black

8

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30 July 2017

10 October 2012

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30 July 2017

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30 July 2017

14

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30 July 2017

3

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30 July 2017

174-180

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Minimal incidence of neonatal/infancy onset diabetes in Italy is 1:90,000 live births

30 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4101463

Permanent diabetes during the first year of life: multiple gene screening in 54 patients

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4101463

Harmonization of glutamic acid decarboxylase and islet antigen-2 autoantibody assays for national institute of diabetes and digestive and kidney diseases consortia

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4101463

Update of mutations in the genes encoding the pancreatic beta-cell K(ATP) channel subunits Kir6.2 (KCNJ11) and sulfonylurea receptor 1 (ABCC8) in diabetes mellitus and hyperinsulinism

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4101463

Diagnosis and treatment of neonatal diabetes: a United States experience

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4101463

Clinical implications of a molecular genetic classification of monogenic beta-cell diabetes

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4101463

The G53D mutation in Kir6.2 (KCNJ11) is associated with neonatal diabetes and motor dysfunction in adulthood that is improved with sulfonylurea therapy

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4101463

Neonatal diabetes mellitus: a disease linked to multiple mechanisms

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4101463

Activating mutations in the ABCC8 gene in neonatal diabetes mellitus

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4101463

Mutations in the Kir6.2 subunit of the KATP channel and permanent neonatal diabetes: new insights and new treatment

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4101463

Activating mutations in the gene encoding the ATP-sensitive potassium-channel subunit Kir6.2 and permanent neonatal diabetes

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4101463

Glucokinase (GCK) mutations in hyper- and hypoglycemia: Maturity-onset diabetes of the young, permanent neonatal diabetes, and hyperinsulinemia of infancy

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4101463

A diabetes-susceptible HLA haplotype is best defined by a combination of HLA-DR and -DQ alleles

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4101463

Mutations in KCNJ11, which encodes Kir6.2, are a common cause of diabetes diagnosed in the first 6 months of life, with the phenotype determined by genotype.

5 July 2018

1 reference

https://api.crossref.org/works/10.1111%2FPEDI.12003

Insulin mutation screening in 1,044 patients with diabetes: mutations in the INS gene are a common cause of neonatal diabetes but a rare cause of diabetes diagnosed in childhood or adulthood

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FPEDI.12003

Switching from insulin to oral sulfonylureas in patients with diabetes due to Kir6.2 mutations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FPEDI.12003

Effective treatment with oral sulfonylureas in patients with diabetes due to sulfonylurea receptor 1 (SUR1) mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FPEDI.12003

KCNJ11 activating mutations are associated with developmental delay, epilepsy and neonatal diabetes syndrome and other neurological features.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FPEDI.12003

SEARCH for Diabetes in Youth: a multicenter study of the prevalence, incidence and classification of diabetes mellitus in youth

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FPEDI.12003

Incidence of diabetes in youth in the United States

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FPEDI.12003

Referral rates for diagnostic testing support an incidence of permanent neonatal diabetes in three European countries of at least 1 in 260,000 live births

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FPEDI.12003

Prevalence of permanent neonatal diabetes in Slovakia and successful replacement of insulin with sulfonylurea therapy in KCNJ11 and ABCC8 mutation carriers

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FPEDI.12003

Improved motor development and good long-term glycaemic control with sulfonylurea treatment in a patient with the syndrome of intermediate developmental delay, early-onset generalised epilepsy and neonatal diabetes associated with the V59M mutation i

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FPEDI.12003

HLA genotyping supports a nonautoimmune etiology in patients diagnosed with diabetes under the age of 6 months

21 January 2018

1 reference

12 December 2020

The burden of diabetes mellitus among US youth: prevalence estimates from the SEARCH for Diabetes in Youth Study

1 reference

12 December 2020

Neonatal diabetes mellitus

1 reference

12 December 2020

Permanent diabetes mellitus in the first year of life

1 reference

12 December 2020

Identifiers

DOI

10.1111/PEDI.12003

1 reference

release_h4blj4meezagpbslg3ofuno4ka

30 July 2017

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/h4blj4meezagpbslg3ofuno4ka

24 November 2022

mapped directly with Wikidata item

PMCID

4101463

1 reference

30 July 2017

1 reference