(Q46853690)

25 December 2017

title

Molecular and immunohistochemical analyses of the focal form of congenital hyperinsulinism (English)

1 reference

25 December 2017

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Charles A Stanley

7

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author name string

Mariko Suchi

1

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25 December 2017

Courtney M MacMullen

2

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25 December 2017

Paul S Thornton

3

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25 December 2017

N Scott Adzick

4

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25 December 2017

Arupa Ganguly

5

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25 December 2017

Eduardo D Ruchelli

6

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25 December 2017

publication date

1 January 2006

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25 December 2017

number of pages

8

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inferred from page(s)

published in

Modern Pathology

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25 December 2017

volume

19

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25 December 2017

issue

1

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25 December 2017

page(s)

122-129

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25 December 2017

Beta cell nesidioblastosis in idiopathic hypoglycemia of infancy

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7 January 2021

The basic structural lesion of persistent neonatal hypoglycaemia with hyperinsulinism: deficiency of pancreatic D cells or hyperactivity of B cells?

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Genetics of neonatal hyperinsulinism.

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Familial hyperinsulinism caused by an activating glucokinase mutation

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

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7 January 2021

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

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7 January 2021

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

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7 January 2021

Reconstitution of IKATP: an inward rectifier subunit plus the sulfonylurea receptor

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7 January 2021

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

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7 January 2021

A nonsense mutation in the inward rectifier potassium channel gene, Kir6.2, is associated with familial hyperinsulinism

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https://api.crossref.org/works/10.1038%2FMODPATHOL.3800497

7 January 2021

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

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7 January 2021

Mutations in the sulonylurea receptor gene are associated with familial hyperinsulinism in Ashkenazi Jews.

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7 January 2021

A multidisciplinary approach to the focal form of congenital hyperinsulinism leads to successful treatment by partial pancreatectomy

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7 January 2021

Congenital Hyperinsulinism

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7 January 2021

Somatic deletion of the imprinted 11p15 region in sporadic persistent hyperinsulinemic hypoglycemia of infancy is specific of focal adenomatous hyperplasia and endorses partial pancreatectomy

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7 January 2021

Paternal mutation of the sulfonylurea receptor (SUR1) gene and maternal loss of 11p15 imprinted genes lead to persistent hyperinsulinism in focal adenomatous hyperplasia

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7 January 2021

Relaxation of imprinted genes in human cancer.

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Relaxation of insulin-like growth factor II gene imprinting implicated in Wilms' tumour

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7 January 2021

Imprinting of the gene encoding a human cyclin-dependent kinase inhibitor, p57KIP2, on chromosome 11p15

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7 January 2021

Cloning of p57KIP2, a cyclin-dependent kinase inhibitor with unique domain structure and tissue distribution

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7 January 2021

p57KIP2, a structurally distinct member of the p21CIP1 Cdk inhibitor family, is a candidate tumor suppressor gene

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p57(KIP2) expression in normal islet cells and in hyperinsulinism of infancy.

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7 January 2021

Preoperative evaluation of infants with focal or diffuse congenital hyperinsulinism by intravenous acute insulin response tests and selective pancreatic arterial calcium stimulation

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7 January 2021

Beta-cell proliferation and apoptosis in the developing normal human pancreas and in hyperinsulinism of infancy

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7 January 2021

Histopathology of congenital hyperinsulinism: retrospective study with genotype correlations

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7 January 2021

Conformation-sensitive gel electrophoresis for rapid detection of single-base differences in double-stranded PCR products and DNA fragments: evidence for solvent-induced bends in DNA heteroduplexes

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7 January 2021

Sensitivity of conformation sensitive gel electrophoresis in detecting mutations in Marfan syndrome and related conditions

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7 January 2021

10.1038/MODPATHOL.3800497

Identifiers

DOI

1 reference

25 December 2017

1 reference

25 December 2017