(Q51576109)

7 April 2018

title

A syndrome of congenital hyperinsulinism and hyperammonemia. (English)

1 reference

7 April 2018

author

Gerard Berry

3

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7 April 2018

Charles A Stanley

1 reference

ORCID Public Data File 2021

author name string

Weinzimer SA

1

1 reference

7 April 2018

Stanley CA

2

1 reference

7 April 2018

Yudkoff M

4

1 reference

7 April 2018

Tuchman M

5

1 reference

7 April 2018

Thornton PS

6

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7 April 2018

language of work or name

English

0 references

publication date

1 April 1997

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7 April 2018

The Journal of Pediatrics

published in

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7 April 2018

volume

130

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7 April 2018

page(s)

661-664

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7 April 2018

issue

4

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7 April 2018

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

cites work

1 reference

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Nesidioblastosis: evidence for autosomal recessive inheritance

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2897%2970256-7

Persistent hyperinsulinemic hypoglycemia of infancy (“nesidioblastosis”): Autosomal recessive inheritance in 7 pedigrees

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2897%2970256-7

Cloning of the beta cell high-affinity sulfonylurea receptor: a regulator of insulin secretion

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2897%2970256-7

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2897%2970256-7

Familial hyperinsulinism maps to chromosome 11p14-15.1, 30 cM centromeric to the insulin gene

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2897%2970256-7

Glycemic response to glucagon during fasting hypoglycemia: an aid in the diagnosis of hyperinsulinism.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2897%2970256-7

N-acetylglutamate synthetase (NAGS) deficiency: diagnosis, clinical observations and treatment

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2897%2970256-7

Late-onset form of partial N-acetylglutamate synthetase deficiency

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2897%2970256-7

N ‐acetylglutamate synthetase deficiency: Clinical and laboratory observations

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2897%2970256-7

N-acetylglutamate synthetase deficiency: diagnosis, management and follow-up of a rare disorder of ammonia detoxication

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2897%2970256-7

Partial N-acetylglutamate synthetase deficiency: a new case with uncontrollable movement disorders

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2897%2970256-7

Normal N-acetylglutamate concentration measured in liver from a new patient with N-acetylglutamate synthetase deficiency: physiologic and biochemical implications

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2897%2970256-7

L-leucine and a nonmetabolized analogue activate pancreatic islet glutamate dehydrogenase

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2897%2970256-7

Insulin release: reconciliation of the receptor and metabolic hypotheses. Nutrient receptors in islet cells

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2897%2970256-7

10.1016/S0022-3476(97)70256-7

7 January 2021

Identifiers

DOI

1 reference

7 April 2018

PubMed ID

9108870

1 reference

7 April 2018