(Q43985793)

28 November 2017

Compound heterozygosity for the common sulfonylurea receptor mutations can cause mild diazoxide-sensitive hyperinsulinism (English)

1 reference

28 November 2017

1 reference

3

Dalit Modan-Moses

1 reference

28 November 2017

Benjamin Dekel

1

1 reference

28 November 2017

Daniel Lubin

2

1 reference

28 November 2017

Jacob Quint

4

1 reference

28 November 2017

Benjamin Glaser

5

1 reference

28 November 2017

Joseph Meyerovitch

6

1 reference

28 November 2017

1 April 2002

1 reference

28 November 2017

1 reference

28 November 2017

41

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28 November 2017

183-186

1 reference

28 November 2017

3

1 reference

Hyperinsulinism in infants and children

28 November 2017

1 reference

https://api.crossref.org/works/10.1177%2F000992280204100310

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F000992280204100310

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F000992280204100310

Familial and sporadic hyperinsulinism: histopathologic findings and segregation analysis support a single autosomal recessive disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F000992280204100310

Familial hyperinsulinism caused by an activating glucokinase mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F000992280204100310

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F000992280204100310

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

1 reference

https://api.crossref.org/works/10.1177%2F000992280204100310

Surgical treatment of hyperinsulinaemic hypoglycaemia in infancy and childhood

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F000992280204100310

Functional analyses of novel mutations in the sulfonylurea receptor 1 associated with persistent hyperinsulinemic hypoglycemia of infancy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F000992280204100310

Familial hyperinsulinism with apparent autosomal dominant inheritance: Clinical and genetic differences from the autosomal recessive variant

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F000992280204100310

Genetic heterogeneity in familial hyperinsulinism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F000992280204100310

Intragenic single nucleotide polymorphism haplotype analysis of SUR1 mutations in familial hyperinsulinism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F000992280204100310

10.1177/000992280204100310

21 January 2018

Identifiers

DOI

1 reference

release_n5krnkmhdfektnp3dotnvce3le

28 November 2017

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/n5krnkmhdfektnp3dotnvce3le

mapped directly with Wikidata item

24 November 2022

based on heuristic

1 reference