Nateglinide is Effective for Diabetes Mellitus with Reactive Hypoglycemia in a Child with a Compound Heterozygous ABCC8 Mutation.

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ABCC8 R1420H Loss-of-Function Variant in a Southwest American Indian Community: Association With Increased Birth Weight and Doubled Risk of Type 2 Diabetes.

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Nateglinide is Effective for Diabetes Mellitus with Reactive Hypoglycemia in a Child with a Compound Heterozygous ABCC8 Mutation.

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2012 nî lūn-bûn

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2012年学术文章

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Nateglinide is Effective for D ...... d Heterozygous ABCC8 Mutation.

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Nateglinide is Effective for D ...... d Heterozygous ABCC8 Mutation.

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type

Item

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Nateglinide is Effective for D ...... d Heterozygous ABCC8 Mutation.

@en

Nateglinide is Effective for D ...... d Heterozygous ABCC8 Mutation.

@nl

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Nateglinide is Effective for D ...... d Heterozygous ABCC8 Mutation.

@en

Nateglinide is Effective for D ...... d Heterozygous ABCC8 Mutation.

@nl

P1476

Nateglinide is Effective for D ...... d Heterozygous ABCC8 Mutation.

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Akiko Saito-Hakoda

http://www.w3.org/2001/XMLSchema#string

Ikuma Fujiwara

http://www.w3.org/2001/XMLSchema#string

Junko Kanno

http://www.w3.org/2001/XMLSchema#string

Shigeo Kure

http://www.w3.org/2001/XMLSchema#string

Tohru Yorifuji

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P2860

Mutation of the pancreatic islet inward rectifier Kir6.2 also leads to familial persistent hyperinsulinemic hypoglycemia of infancy

Inactivation of the first nucleotide-binding fold of the sulfonylurea receptor, and familial persistent hyperinsulinemic hypoglycemia of infancy

Glucose induces closure of single potassium channels in isolated rat pancreatic beta-cells

Dysregulation of insulin secretion in children with congenital hyperinsulinism due to sulfonylurea receptor mutations

Molecular and clinical analysis of Japanese patients with persistent congenital hyperinsulinism: predominance of paternally inherited monoallelic mutations in the KATP channel genes.

ATP-sensitive potassium channelopathies: focus on insulin secretion

Postprandial reactive hypoglycemia.

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

Abnormalities of pancreatic islets by targeted expression of a dominant-negative KATP channel.

Novel de novo mutation in sulfonylurea receptor 1 presenting as hyperinsulinism in infancy followed by overt diabetes in early adolescence

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45-52

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scholarly article

case report

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10.1297/CPE.21.45

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http://www.w3.org/2001/XMLSchema#string

P478

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2012-07-25T00:00:00Z

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255707495

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23926410

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P921

hypoglycemia

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3687649

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Nateglinide is Effective for Diabetes Mellitus with Reactive Hypoglycemia in a Child with a Compound Heterozygous ABCC8 Mutation.

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P2860

P2860

Nateglinide is Effective for Diabetes Mellitus with Reactive Hypoglycemia in a Child with a Compound Heterozygous ABCC8 Mutation.

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P1433

P1476

P2093

P2860

P304

P31

P356

P433

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P5875

P698

P921

P932

P356

P1433

P1476

P2093

P2860

P304

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P356

P433

P478

P577

P5875

P698

P921

P932