(Q51471646)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21518169%20AND%20SRC:MED&resulttype=core&format=json

29 January 2020

title

Familial occurrence of neonatal diabetes with duplications in chromosome 6q24: treatment with sulfonylurea and 40-yr follow-up (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21518169%20AND%20SRC:MED&resulttype=core&format=json

29 January 2020

7

1 reference

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29 January 2020

Deborah Jg Mackay

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21518169%20AND%20SRC:MED&resulttype=core&format=json

29 January 2020

Karen Temple

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21518169%20AND%20SRC:MED&resulttype=core&format=json

29 January 2020

1

Oddmund Søvik

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21518169%20AND%20SRC:MED&resulttype=core&format=json

29 January 2020

6

Anders Molven

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21518169%20AND%20SRC:MED&resulttype=core&format=json

29 January 2020

author name string

Oystein Aagenaes

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21518169%20AND%20SRC:MED&resulttype=core&format=json

29 January 2020

Stig Å Eide

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21518169%20AND%20SRC:MED&resulttype=core&format=json

29 January 2020

publication date

24 April 2011

1 reference

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29 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21518169%20AND%20SRC:MED&resulttype=core&format=json

29 January 2020

volume

13

1 reference

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29 January 2020

issue

2

1 reference

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29 January 2020

page(s)

155-162

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21518169%20AND%20SRC:MED&resulttype=core&format=json

Neonatal hyperglycaemia: case report with plasma insulin studies

29 January 2020

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-5448.2011.00776.X

Transient neonatal diabetes mellitus in sibs

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-5448.2011.00776.X

Aetiology of transient neonatal diabetes

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-5448.2011.00776.X

Refinement of the 6q chromosomal region implicated in transient neonatal diabetes

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-5448.2011.00776.X

Transient neonatal diabetes, a disorder of imprinting.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-5448.2011.00776.X

The C42R mutation in the Kir6.2 (KCNJ11) gene as a cause of transient neonatal diabetes, childhood diabetes, or later-onset, apparently type 2 diabetes mellitus.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-5448.2011.00776.X

Activating mutations in the ABCC8 gene in neonatal diabetes mellitus

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-5448.2011.00776.X

Transient and permanent neonatal diabetes

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-5448.2011.00776.X

Quantitative analysis of SNRPN(correction of SRNPN) gene methylation by pyrosequencing as a diagnostic test for Prader-Willi syndrome and Angelman syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-5448.2011.00776.X

Beta-cell dysfunction in classic transient neonatal diabetes is characterized by impaired insulin response to glucose but normal response to glucagon.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-5448.2011.00776.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-5448.2011.00776.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-5448.2011.00776.X

Long-term course of neonatal diabetes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-5448.2011.00776.X

Genetic and epigenetic defects at the 6q24 imprinted locus in a cohort of 13 patients with transient neonatal diabetes: new hypothesis raised by the finding of a unique case with hemizygotic deletion in the critical region

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-5448.2011.00776.X

Epimutation of the TNDM locus and the Beckwith–Wiedemann syndrome centromeric locus in individuals with transient neonatal diabetes mellitus

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-5448.2011.00776.X

10.1111/J.1399-5448.2011.00776.X

21 January 2018

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21518169%20AND%20SRC:MED&resulttype=core&format=json

29 January 2020

1 reference