Clinical presentation and management of children with diffuse and focal hyperinsulinism: a review of 223 cases. (Q37275929)

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22 February 2020

title

Clinical presentation and management of children with diffuse and focal hyperinsulinism: a review of 223 cases (English)

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22 February 2020

5

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22 February 2020

author name string

Katherine Lord

1

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22 February 2020

Enyo Dzata

2

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22 February 2020

Kara E Snider

3

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22 February 2020

Paul R Gallagher

4

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22 February 2020

language of work or name

English

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publication date

20 September 2013

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The Journal of Clinical Endocrinology and Metabolism

22 February 2020

published in

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22 February 2020

volume

98

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22 February 2020

page(s)

E1786-9

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issue

11

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Genotype and phenotype correlations in 417 children with congenital hyperinsulinism

22 February 2020

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3816257

Glucose metabolism in 105 children and adolescents after pancreatectomy for congenital hyperinsulinism

6 September 2017

1 reference

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Morphological mosaicism of the pancreatic islets: a novel anatomopathological form of persistent hyperinsulinemic hypoglycemia of infancy

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3816257

Postnatal glucose homeostasis in late-preterm and term infants

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3816257

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

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3816257

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

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3816257

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

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3816257

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

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3816257

Monogenic hyperinsulinemic hypoglycemia: current insights into the pathogenesis and management

6 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3816257

26 June 2018

Identifiers

DOI

10.1210/JC.2013-2094

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22 February 2020

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22 February 2020

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