(Q36604826)

15 August 2017

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title

Molecular mechanisms of neonatal hyperinsulinism (English)

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15 August 2017

10

Claire Nihoul-Fékété

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Christine Bellanné-Chantelot

15 August 2017

2

object named as

Christine Bellanné-Chantelot

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15 August 2017

13

Pascale de Lonlay

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15 August 2017

Irina Giurgea

1

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15 August 2017

Maria Ribeiro

3

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15 August 2017

Laurence Hubert

4

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15 August 2017

Christine Sempoux

5

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15 August 2017

Jean-Jacques Robert

6

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15 August 2017

Oliver Blankenstein

7

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15 August 2017

Kahlid Hussain

8

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15 August 2017

Francis Brunelle

9

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Jacques Rahier

11

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Francis Jaubert

12

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publication date

26 September 2006

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15 August 2017

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15 August 2017

volume

66

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15 August 2017

issue

6

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15 August 2017

page(s)

289-296

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Hypoglycemia in infancy and childhood. Part I

15 August 2017

cites work

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Practical management of hyperinsulinism in infancy

21 January 2018

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Clinical features of 52 neonates with hyperinsulinism.

21 January 2018

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Mutations in the sulonylurea receptor gene are associated with familial hyperinsulinism in Ashkenazi Jews.

21 January 2018

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Familial hyperinsulinism caused by an activating glucokinase mutation

21 January 2018

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Hyperinsulinism and hyperammonemia in infants with regulatory mutations of the glutamate dehydrogenase gene

21 January 2018

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Hyperinsulinism in short-chain L-3-hydroxyacyl-CoA dehydrogenase deficiency reveals the importance of beta-oxidation in insulin secretion

21 January 2018

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Facial appearance in persistent hyperinsulinemic hypoglycemia

21 January 2018

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Central nervous system hyperexcitability associated with glutamate dehydrogenase gain of function mutations

21 January 2018

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Heterogeneity of persistent hyperinsulinaemic hypoglycaemia. A series of 175 cases

21 January 2018

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Clinical and genetic heterogeneity in congenital hyperinsulinism

21 January 2018

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Long-term treatment of persistent hyperinsulinaemic hypoglycaemia of infancy with diazoxide: a retrospective review of 77 cases and analysis of efficacy-predicting criteria.

21 January 2018

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Factitious hyperinsulinism leading to pancreatectomy: severe forms of Munchausen syndrome by proxy

21 January 2018

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BPDZ 154 activates adenosine 5'-triphosphate-sensitive potassium channels: in vitro studies using rodent insulin-secreting cells and islets isolated from patients with hyperinsulinism

21 January 2018

1 reference

Genetics of neonatal hyperinsulinism.

21 January 2018

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Hyperinsulinism in infancy: from basic science to clinical disease.

21 January 2018

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Mutations in the genes encoding the pancreatic beta-cell KATP channel subunits Kir6.2 (KCNJ11) and SUR1 (ABCC8) in diabetes mellitus and hyperinsulinism

21 January 2018

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Mutation spectra of ABCC8 gene in Spanish patients with Hyperinsulinism of Infancy (HI).

21 January 2018

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Unbalanced expression of 11p15 imprinted genes in focal forms of congenital hyperinsulinism: association with a reduction to homozygosity of a mutation in ABCC8 or KCNJ11

21 January 2018

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Persistent hyperinsulinaemic hypoglycaemia of infancy: a heterogeneous syndrome unrelated to nesidioblastosis

21 January 2018

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Epigenetic alterations of H19 and LIT1 distinguish patients with Beckwith-Wiedemann syndrome with cancer and birth defects

21 January 2018

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Paradoxical NSD1 mutations in Beckwith-Wiedemann syndrome and 11p15 anomalies in Sotos syndrome

21 January 2018

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Uniparental paternal disomy in a genetic cancer-predisposing syndrome

21 January 2018

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Disruption of insulin-like growth factor 2 imprinting in Beckwith-Wiedemann syndrome

21 January 2018

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An imprinted gene p57KIP2 is mutated in Beckwith-Wiedemann syndrome

21 January 2018

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Congenital hyperinsulinism and mosaic abnormalities of the ploidy

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1159/000095938

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release_q6rrtpgtjfh3xlfjv6axucquyi

15 August 2017

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/q6rrtpgtjfh3xlfjv6axucquyi

mapped directly with Wikidata item

24 November 2022

based on heuristic

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