Clinical presentation and management of children with diffuse and focal hyperinsulinism: a review of 223 cases. - Wikidata - wikimedia - TriplyDB

Clinical presentation and management of children with diffuse and focal hyperinsulinism: a review of 223 cases.

Clinical presentation and management of children with diffuse and focal hyperinsulinism: a review of 223 cases.

http://www.wikidata.org/entity/Q37275929

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Monoallelic ABCC8 mutations are a common cause of diazoxide-unresponsive diffuse form of congenital hyperinsulinism Long-term medical treatment in congenital hyperinsulinism: a descriptive analysis in a large cohort of patients from different clinical centers The Diagnosis and Management of Hyperinsulinaemic Hypoglycaemia Clinical and molecular data from 61 Brazilian cases of Congenital Hyperinsulinemic Hypoglycemia.High Risk of Diabetes and Neurobehavioral Deficits in Individuals With Surgically Treated Hyperinsulinism.Enhanced Islet Cell Nucleomegaly Defines Diffuse Congenital Hyperinsulinism in Infancy but Not Other Forms of the Disease Late Presentation of Fulminant Necrotizing Enterocolitis in a Child with Hyperinsulinism on Octreotide Therapy Clinical practice guidelines for congenital hyperinsulinism.A Novel Homozygous Mutation in the KCNJ11 Gene of a Neonate with Congenital Hyperinsulinism and Successful Management with Sirolimus.Diagnosis and treatment of hyperinsulinaemic hypoglycaemia and its implications for paediatric endocrinology.Clinical and Genetic Characteristics, Management and Long-Term Follow-Up of Turkish Patients with Congenital Hyperinsulinism.Functional and Metabolomic Consequences of KATP Channel Inactivation in Human Islets.18F-DOPA PET/CT and 68Ga-DOTANOC PET/CT scans as diagnostic tools in focal congenital hyperinsulinism: a blinded evaluation.A Multicenter Experience with Long-Acting Somatostatin Analogues in Patients with Congenital Hyperinsulinism.Formal Neurocognitive Testing in 60 Patients with Congenital Hyperinsulinism.Population pharmacokinetics of exendin-(9-39) and clinical dose selection in patients with congenital hyperinsulinism.Congenital Hyperinsulinism: Diagnosis and Treatment Update.A unique allosteric insulin receptor monoclonal antibody that prevents hypoglycemia in the SUR-1(/( mouse model of KATP hyperinsulinism.The Role of KCNQ1 Mutations and Maternal Beta Blocker Use During Pregnancy in the Growth of Children With Long QT Syndrome.Clinical Diversity in Focal Congenital Hyperinsulinism in Infancy Correlates With Histological Heterogeneity of Islet Cell Lesions Intraoperative Ultrasound: A Tool to Support Tissue-Sparing Curative Pancreatic Resection in Focal Congenital Hyperinsulinism

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P2860

Clinical presentation and management of children with diffuse and focal hyperinsulinism: a review of 223 cases.

http://www.wikidata.org/entity/Q37275929

description

article científic

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article scientifique

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articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on 20 September 2013

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vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

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name

Clinical presentation and mana ...... linism: a review of 223 cases.

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Clinical presentation and mana ...... linism: a review of 223 cases.

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type

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Clinical presentation and mana ...... linism: a review of 223 cases.

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Clinical presentation and mana ...... linism: a review of 223 cases.

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prefLabel

Clinical presentation and mana ...... linism: a review of 223 cases.

@en

Clinical presentation and mana ...... linism: a review of 223 cases.

@nl

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The Journal of Clinical Endocrinology and Metabolism

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Clinical presentation and mana ...... ulinism: a review of 223 cases

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Enyo Dzata

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Kara E Snider

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Katherine Lord

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Paul R Gallagher

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P2860

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

Postnatal glucose homeostasis in late-preterm and term infants.

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

Glucose metabolism in 105 children and adolescents after pancreatectomy for congenital hyperinsulinism.

Genotype and phenotype correlations in 417 children with congenital hyperinsulinism

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

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

Morphological mosaicism of the pancreatic islets: a novel anatomopathological form of persistent hyperinsulinemic hypoglycemia of infancy.

Monogenic hyperinsulinemic hypoglycemia: current insights into the pathogenesis and management.

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10.1210/JC.2013-2094

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