(Q33700991)

English

Disease progression and search for monogenic diabetes among children with new onset type 1 diabetes negative for ICA, GAD- and IA-2 Antibodies

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Disease progression and search for monogenic diabetes among children with new onset type 1 diabetes negative for ICA, GAD- and IA-2 Antibodies (English)

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

type-1 diabetes

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object named as

Sven Pörksen

1

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object named as

Heidi de Wet

6

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Henrik B Mortensen

object named as

Henrik B Mortensen

17

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object named as

Mikael Knip

16

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Pål R Njølstad

19

object named as

Pål R Njølstad

1 reference

Europe PubMed Central

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28 July 2017

15

object named as

Anders Molven

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28 July 2017

Frances Ashcroft

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object named as

Frances Ashcroft

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28 July 2017

Carine de Beaufort

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object named as

Carine de Beaufort

1 reference

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28 July 2017

author name string

Lene Bjerke Laborie

2

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28 July 2017

Lotte Nielsen

3

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28 July 2017

Marie Louise Max Andersen

4

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28 July 2017

Tone Sandal

5

1 reference

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28 July 2017

Erik Schwarcz

7

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28 July 2017

Jan Aman

8

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28 July 2017

Peter Swift

9

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28 July 2017

Mirjana Kocova

10

1 reference

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28 July 2017

Eugen J Schönle

11

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28 July 2017

Philip Hougaard

13

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28 July 2017

Lars Hansen

18

1 reference

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28 July 2017

Hvidøre Study Group on Childhood Diabetes

20

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28 July 2017

publication date

23 September 2010

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Europe PubMed Central

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28 July 2017

BMC Endocrine Disorders

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Europe PubMed Central

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28 July 2017

10

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16

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28 July 2017

copyright license

Creative Commons Attribution 2.0 Generic

23 September 2010

1 reference

April 2022 Public Data File from Crossref

copyright status

1 reference

April 2022 Public Data File from Crossref

Zinc transporter 8 antibodies complement GAD and IA-2 antibodies in the identification and characterization of adult-onset autoimmune diabetes: Non Insulin Requiring Autoimmune Diabetes (NIRAD) 4.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2955624

21 June 2018

New definition for the partial remission period in children and adolescents with type 1 diabetes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2955624

21 June 2018

Seven mutations in the human insulin gene linked to permanent neonatal/infancy-onset diabetes mellitus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2955624

21 June 2018

Insulin gene mutations as a cause of permanent neonatal diabetes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2955624

21 June 2018

Activating mutations in the ABCC8 gene in neonatal diabetes mellitus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2955624

21 June 2018

A hepatocyte nuclear factor-4 alpha gene (HNF4A) P2 promoter haplotype linked with late-onset diabetes: studies of HNF4A variants in the Norwegian MODY registry

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2955624

21 June 2018

A heterozygous activating mutation in the sulphonylurea receptor SUR1 (ABCC8) causes neonatal diabetes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2955624

21 June 2018

Clinical characteristics, beta-cell function, HLA class II and mutations in MODY genes in non-paediatric subjects with Type 1 diabetes without pancreatic autoantibodies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2955624

21 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2955624

21 June 2018

Molecular mechanisms and clinical pathophysiology of maturity-onset diabetes of the young

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2955624

21 June 2018

Mutations in the hepatocyte nuclear factor-4alpha gene in maturity-onset diabetes of the young (MODY1)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2955624

21 June 2018

Mutations in the hepatocyte nuclear factor-1alpha gene in maturity-onset diabetes of the young (MODY3)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2955624

21 June 2018

Neonatal diabetes mellitus due to complete glucokinase deficiency

1 reference

https://api.crossref.org/works/10.1186%2F1472-6823-10-16

21 January 2018

Permanent neonatal diabetes due to mutations in KCNJ11 encoding Kir6.2: patient characteristics and initial response to sulfonylurea therapy

1 reference

https://api.crossref.org/works/10.1186%2F1472-6823-10-16

21 January 2018

Glibenclamide treatment in permanent neonatal diabetes mellitus due to an activating mutation in Kir6.2.

1 reference

https://api.crossref.org/works/10.1186%2F1472-6823-10-16

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1186%2F1472-6823-10-16

21 January 2018

IA-2 antibodies--a sensitive marker of IDDM with clinical onset in childhood and adolescence. Childhood Diabetes in Finland Study Group.

1 reference

https://api.crossref.org/works/10.1186%2F1472-6823-10-16

21 January 2018

Mutations in the insulin gene can cause MODY and autoantibody-negative type 1 diabetes

1 reference

https://api.crossref.org/works/10.1186%2F1472-6823-10-16

21 January 2018

The spectrum of ABCC8 mutations in Norwegian patients with congenital hyperinsulinism of infancy.

1 reference

https://api.crossref.org/works/10.1186%2F1472-6823-10-16

21 January 2018

Testing for monogenic diabetes among children and adolescents with antibody-negative clinically defined Type 1 diabetes

1 reference

https://api.crossref.org/works/10.1186%2F1472-6823-10-16

21 January 2018

Impact of IDDM2 on disease pathogenesis and progression in children with newly diagnosed type 1 diabetes: reduced insulin antibody titres and preserved beta cell function

1 reference

https://api.crossref.org/works/10.1186%2F1472-6823-10-16

21 January 2018

A novel micro-assay for insulin autoantibodies

1 reference

https://pubmed.ncbi.nlm.nih.gov/20863361

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in ATP-Sensitive K+ Channel Genes Cause Transient Neonatal Diabetes and Permanent Diabetes in Childhood or Adulthood

1 reference

https://pubmed.ncbi.nlm.nih.gov/20863361

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hepatocyte nuclear factor-1 alpha gene mutations and diabetes in Norway

1 reference

https://pubmed.ncbi.nlm.nih.gov/20863361

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Glutamic acid decarboxylase autoantibody assay using 125I-labelled recombinant GAD65 produced in yeast

1 reference

https://pubmed.ncbi.nlm.nih.gov/20863361

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Diabetes-associated autoantibodies in relation to clinical characteristics and natural course in children with newly diagnosed type 1 diabetes. The Childhood Diabetes In Finland Study Group

1 reference

https://pubmed.ncbi.nlm.nih.gov/20863361

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1186/1472-6823-10-16

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Dimensions Publication ID

0 references

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

ResearchGate publication ID

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