(Q51374595)

4 April 2018

title

Persistently autoantibody negative (PAN) type 1 diabetes mellitus in children. (English)

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4 April 2018

1 reference

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Maria E Craig

6

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Sian Ellard

object named as

Sian Ellard

2

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Andrew Tym Hattersley

10

object named as

Andrew T Hattersley

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4 April 2018

9

George S Eisenbarth

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4 April 2018

author name string

Shihab Hameed

1

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Helen J Woodhead

3

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Kristen A Neville

4

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Jan L Walker

5

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Taylor Armstrong

7

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Liping Yu

8

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Charles F Verge

11

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publication date

6 September 2010

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4 April 2018

published in

Pediatric Diabetes

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volume

12

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issue

3 Pt 1

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page(s)

142-149

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4 April 2018

A genetic diagnosis of HNF1A diabetes alters treatment and improves glycaemic control in the majority of insulin-treated patients.

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-5448.2010.00681.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-5448.2010.00681.X

Best practice guidelines for the molecular genetic diagnosis of maturity-onset diabetes of the young

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-5448.2010.00681.X

beta-cell genes and diabetes: molecular and clinical characterization of mutations in transcription factors

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-5448.2010.00681.X

Emerging epidemic of type 2 diabetes in youth

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-5448.2010.00681.X

The cation efflux transporter ZnT8 (Slc30A8) is a major autoantigen in human type 1 diabetes

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-5448.2010.00681.X

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%2FJ.1399-5448.2010.00681.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.1399-5448.2010.00681.X

Insulin gene mutations as cause of diabetes in children negative for five type 1 diabetes autoantibodies

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-5448.2010.00681.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1399-5448.2010.00681.X

10.1111/J.1399-5448.2010.00681.X

21 January 2018

Identifiers

DOI

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4 April 2018

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4 April 2018