(Q44124704)

30 November 2017

Facial appearance in persistent hyperinsulinemic hypoglycemia (English)

1 reference

30 November 2017

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3

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30 November 2017

Valérie Cormier-Daire

object named as

Valérie Cormier-Daire

2

0 references

Claire Nihoul-Fékété

8

object named as

Claire Nihoul-Fékété

1 reference

30 November 2017

Pascale de Lonlay

1

1 reference

30 November 2017

Guy Touati

4

1 reference

30 November 2017

Alice Goldenberg

5

1 reference

30 November 2017

Jean-Christophe Fournet

6

1 reference

30 November 2017

Francis Brunelle

7

1 reference

30 November 2017

Jacques Rahier

9

1 reference

30 November 2017

Claudine Junien

10

1 reference

30 November 2017

Jean-Jacques Robert

11

1 reference

30 November 2017

Jean-Marie Saudubray

12

1 reference

30 November 2017

1 August 2002

1 reference

American Journal of Medical Genetics Part A

30 November 2017

1 reference

30 November 2017

111

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30 November 2017

130-133

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30 November 2017

2

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Somatic deletion of the imprinted 11p15 region in sporadic persistent hyperinsulinemic hypoglycemia of infancy is specific of focal adenomatous hyperplasia and endorses partial pancreatectomy

30 November 2017

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10463

Clinical features of 52 neonates with hyperinsulinism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10463

Familial hyperinsulinism caused by an activating glucokinase mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10463

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10463

Hyperinsulinism in infants and children

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10463

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10463

Neonatal and infantile hypoglycemia due to insulin excess: new aspects of diagnosis and surgical management

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10463

Mutations in the sulfonylurea receptor gene in familial persistent hyperinsulinemic hypoglycemia of infancy

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10463

Mutation of the pancreatic islet inward rectifier Kir6.2 also leads to familial persistent hyperinsulinemic hypoglycemia of infancy

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10463

Paternal mutation of the sulfonylurea receptor (SUR1) gene and maternal loss of 11p15 imprinted genes lead to persistent hyperinsulinism in focal adenomatous hyperplasia

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FAJMG.10463

21 January 2018

Identifiers

DOI

10.1002/AJMG.10463

1 reference

30 November 2017

1 reference