(Q46914816)

26 December 2017

title

Sulfonylurea improves CNS function in a case of intermediate DEND syndrome caused by a mutation in KCNJ11. (English)

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26 December 2017

intermediate DEND syndrome

main subject

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1 reference

1

Wojciech Mlynarski

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26 December 2017

Andrei I Tarasov

2

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Tomasz Klupa

8

Tomasz Klupa

1 reference

26 December 2017

Maciej T Malecki

9

Maciej T Malecki

1 reference

26 December 2017

Iwona Pietrzak

5

Iwona Pietrzak

1 reference

26 December 2017

Agnieszka Gach

3

Agnieszka Gach

1 reference

26 December 2017

author name string

Christophe A Girard

4

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26 December 2017

Lejla Zubcevic

6

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26 December 2017

Jacek Kusmierek

7

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26 December 2017

Frances M Ashcroft

10

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26 December 2017

publication date

1 November 2007

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26 December 2017

Nature Clinical Practice Neurology

published in

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26 December 2017

volume

3

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26 December 2017

issue

11

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26 December 2017

page(s)

640-645

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26 December 2017

Efflux transport of tolbutamide across the blood-brain barrier

cites work

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEURO0640

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/10.1038%2FNCPNEURO0640

7 January 2021

Activating mutations in Kir6.2 and neonatal diabetes: new clinical syndromes, new scientific insights, and new therapy

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEURO0640

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEURO0640

7 January 2021

Transfer to sulphonylurea therapy in adult subjects with permanent neonatal diabetes due to KCNJ11-activating [corrected] mutations: evidence for improvement in insulin sensitivity

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEURO0640

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEURO0640

7 January 2021

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.

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEURO0640

7 January 2021

Molecular basis of Kir6.2 mutations associated with neonatal diabetes or neonatal diabetes plus neurological features

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEURO0640

7 January 2021

Sulphonylurea action revisited: the post-cloning era.

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEURO0640

7 January 2021

Overlapping distribution of K(ATP) channel-forming Kir6.2 subunit and the sulfonylurea receptor SUR1 in rodent brain

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEURO0640

7 January 2021

Distribution and phenotype of neurons containing the ATP-sensitive K+ channel in rat brain

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEURO0640

7 January 2021

Selectivity of repaglinide and glibenclamide for the pancreatic over the cardiovascular K(ATP) channels

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEURO0640

7 January 2021

Single photon emission tomography (SPECT) study of regional cerebral blood flow in normoalbuminuric children and adolescents with type 1 diabetes.

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEURO0640

7 January 2021

Functional analysis of a structural model of the ATP-binding site of the KATP channel Kir6.2 subunit.

1 reference

https://api.crossref.org/works/10.1038%2FNCPNEURO0640

7 January 2021

Identifiers

DOI

10.1038/NCPNEURO0640

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26 December 2017

1 reference

26 December 2017