The hyperinsulinism/hyperammonemia syndrome (Q34624296)

3 August 2017

The hyperinsulinism/hyperammonemia syndrome (English)

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3 August 2017

Charles A Stanley

2

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author name string

Andrew A Palladino

series ordinal

1

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3 August 2017

1 September 2010

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Reviews in Endocrine and Metabolic Disorders

3 August 2017

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3 August 2017

11

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3 August 2017

3

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3 August 2017

171-178

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https://scigraph.springernature.com/pub.10.1007/s11154-010-9146-0

3 August 2017

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cites work

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

1 reference

12 December 2020

Mechanism of hyperinsulinism in short-chain 3-hydroxyacyl-CoA dehydrogenase deficiency involves activation of glutamate dehydrogenase

1 reference

12 December 2020

Hyperinsulinism and hyperammonemia syndrome: report of twelve unrelated patients

1 reference

12 December 2020

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

1 reference

12 December 2020

Systemic activation of glutamate dehydrogenase increases renal ammoniagenesis: implications for the hyperinsulinism/hyperammonemia syndrome

1 reference

12 December 2020

Hyperinsulinism-hyperammonaemia syndrome: novel mutations in the GLUD1 gene and genotype-phenotype correlations

1 reference

12 December 2020

Neurological aspects of hyperinsulinism-hyperammonaemia syndrome

1 reference

12 December 2020

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

1 reference

12 December 2020

Expression, purification and characterization of human glutamate dehydrogenase (GDH) allosteric regulatory mutations

1 reference

12 December 2020

Functional hyperactivity of hepatic glutamate dehydrogenase as a cause of the hyperinsulinism/hyperammonemia syndrome: effect of treatment

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12 December 2020

Regulation of leucine-stimulated insulin secretion and glutamine metabolism in isolated rat islets

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12 December 2020

L-glutamate dehydrogenases: distribution, properties and mechanism.

1 reference

12 December 2020

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

1 reference

12 December 2020

Acute insulin responses to leucine in children with the hyperinsulinism/hyperammonemia syndrome

1 reference

12 December 2020

Hyperinsulinism/hyperammonemia syndrome in children with regulatory mutations in the inhibitory guanosine triphosphate-binding domain of glutamate dehydrogenase

1 reference

12 December 2020

Biochemical evaluation of a patient with a familial form of leucine-sensitive hypoglycemia and concomitant hyperammonemia

1 reference

12 December 2020

Untangling the glutamate dehydrogenase allosteric nightmare

1 reference

12 December 2020

Familial hypoglycemia precipitated by amino acids

1 reference

12 December 2020

Myoclonic absence epilepsy with photosensitivity and a gain of function mutation in glutamate dehydrogenase

1 reference

12 December 2020

Short term regulation of ureagenesis

1 reference

12 December 2020

Molecular basis and characterization of the hyperinsulinism/hyperammonemia syndrome: predominance of mutations in exons 11 and 12 of the glutamate dehydrogenase gene. HI/HA Contributing Investigators

1 reference

12 December 2020

A syndrome of congenital hyperinsulinism and hyperammonemia.

1 reference

12 December 2020

Structures of bovine glutamate dehydrogenase complexes elucidate the mechanism of purine regulation

1 reference

12 December 2020

10.1007/S11154-010-9146-0

Identifiers

DOI

1 reference

PubMed ID

20936362

Dimensions Publication ID

3 August 2017

0 references

1 reference

PubMed ID

20936362