(Q57499742)

English

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

scientific article published on 01 January 1998

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9 November 2019

Familial hyperinsulinism with apparent autosomal dominant inheritance: clinical and genetic differences from the autosomal recessive variant (English)

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9 November 2019

Benjamin Glaser

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9 November 2019

Charles A Stanley

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9 November 2019

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K Herold

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9 November 2019

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P S Thornton

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9 November 2019

M S Satin-Smith

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9 November 2019

K C Chiu

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9 November 2019

A Nestorowicz

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9 November 2019

M A Permutt

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9 November 2019

L Baker

8

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9 November 2019

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publication date

1 January 1998

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9 November 2019

The Journal of Pediatrics

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9 November 2019

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9 November 2019

9-14

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9 November 2019

1

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9 November 2019

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

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2898%2970477-9

7 January 2021

Nesidioblastosis: evidence for autosomal recessive inheritance

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2898%2970477-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2898%2970477-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2898%2970477-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2898%2970477-9

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2898%2970477-9

7 January 2021

Persistent neonatal hyperinsulinism

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2898%2970477-9

7 January 2021

Short- and long-term use of octreotide in the treatment of congenital hyperinsulinism.

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2898%2970477-9

7 January 2021

Dinucleotide repeat polymorphisms at the D11S419 and CD3D loci

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2898%2970477-9

7 January 2021

Isolation and chromosomal assignment of 100 highly informative human simple sequence repeat polymorphisms

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2898%2970477-9

7 January 2021

Pancreatic and extrapancreatic sulfonylurea receptors

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2898%2970477-9

7 January 2021

Familial hypoglycemia precipitated by amino acids

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2898%2970477-9

7 January 2021

Familial islet-cell adenomatosis

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2898%2970477-9

7 January 2021

Changing concepts of islet cell dysplasia in neonatal and infantile hyperinsulinism

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2898%2970477-9

7 January 2021

Relevance of endocrine pancreas nesidioblastosis to hyperinsulinemic hypoglycemia

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2898%2970477-9

7 January 2021

Nesidioblastosis Associated with Insulin-mediated Hypoglycemia in an Adult

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2898%2970477-9

7 January 2021

Islet cell hyperplasia: an unusual cause of hypoglycemia in an adult.

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2898%2970477-9

7 January 2021

Identifiers

10.1016/S0022-3476(98)70477-9

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9 November 2019

1 reference

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9 November 2019

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