(Q50589680)

16 March 2018

title

Protein-induced hyperinsulinaemic hypoglycaemia due to a homozygous HADH mutation in three siblings of a Saudi family. (English)

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16 March 2018

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Sarah E Flanagan

2

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Sian Ellard

object named as

Sian Ellard

3

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author name string

Omer Babiker

1

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16 March 2018

Hesham Al Girim

4

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16 March 2018

Khalid Hussain

5

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Senthil Senniappan

6

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16 March 2018

publication date

25 April 2015

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16 March 2018

Journal of Pediatric Endocrinology and Metabolism

published in

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16 March 2018

volume

28

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16 March 2018

issue

9-10

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16 March 2018

page(s)

1073-1077

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16 March 2018

Short-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: the clinical relevance of an early diagnosis and report of four new cases.

cites work

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https://api.crossref.org/works/10.1515%2FJPEM-2015-0033

The molecular mechanisms, diagnosis and management of congenital hyperinsulinism

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FJPEM-2015-0033

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FJPEM-2015-0033

Neurologic damage in hypoglycemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FJPEM-2015-0033

Hypoglycemic brain injury

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FJPEM-2015-0033

Clinical characteristics and biochemical mechanisms of congenital hyperinsulinism associated with dominant KATP channel mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FJPEM-2015-0033

Hyperinsulinaemic hypoglycaemia: biochemical basis and the importance of maintaining normoglycaemia during management

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FJPEM-2015-0033

Protein-sensitive and fasting hypoglycemia in children with the hyperinsulinism/hyperammonemia syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FJPEM-2015-0033

Persistent hyperinsulinemic hypoglycemia and maturity-onset diabetes of the young due to heterozygous HNF4A mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FJPEM-2015-0033

Clinical and molecular characterisation of 300 patients with congenital hyperinsulinism

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FJPEM-2015-0033

Hyperinsulinaemic hypoglycaemia: genetic mechanisms, diagnosis and management.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FJPEM-2015-0033

3-Hydroxyacyl-coenzyme A dehydrogenase deficiency and hyperinsulinemic hypoglycemia: characterization of a novel mutation and severe dietary protein sensitivity.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FJPEM-2015-0033

Genome-wide homozygosity analysis reveals HADH mutations as a common cause of diazoxide-responsive hyperinsulinemic-hypoglycemia in consanguineous pedigrees

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FJPEM-2015-0033

Congenital hyperinsulinism: current trends in diagnosis and therapy

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FJPEM-2015-0033

Neurochemical changes in the rat occipital cortex and hippocampus after repetitive and profound hypoglycemia during the neonatal period: an ex vivo ¹H magnetic resonance spectroscopy study

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FJPEM-2015-0033

Novel presentations of congenital hyperinsulinism due to mutations in the MODY genes: HNF1A and HNF4A.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FJPEM-2015-0033

21 January 2018

Identifiers

DOI

10.1515/JPEM-2015-0033

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16 March 2018

PubMed ID

25915078

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16 March 2018