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Recommendations from the Pediatric Endocrine Society for Evaluation and Management of Persistent Hypoglycemia in Neonates, Infants, and Children

The Journal of pediatrics, 2015-08, Vol.167 (2), p.238-245

2015

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Activation of Protein Kinase A (PKA) signaling mitigates congenital hyperinsulinism associated hypoglycemia in the Sur1-/- mouse model

PloS one, 2020-07, Vol.15 (7), p.e0236892-e0236892

2020

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Androgenetic chimerism as an etiology for Beckwith-Wiedemann syndrome: diagnosis and management

Genetics in medicine, 2019-11, Vol.21 (11), p.2644-2649

2019

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The Use of Lanreotide in the Treatment of Congenital Hyperinsulinism

The journal of clinical endocrinology and metabolism, 2022-08, Vol.107 (8), p.e3115-e3120

2022

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What's in a name? That which we call perinatal stress hyperinsulinism by any other name would smell so bitter

Journal of perinatology, 2021-08, Vol.41 (8), p.2110-2110

2021

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Management and Appropriate Use of Diazoxide in Infants and Children with Hyperinsulinism

The journal of clinical endocrinology and metabolism, 2020-12, Vol.105 (12), p.1-3761

2020

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The Role of GLP-1 Signaling in Hypoglycemia due to Hyperinsulinism

Frontiers in endocrinology (Lausanne), 2022-03, Vol.13, p.863184-863184

2022

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Re-Evaluating “Transitional Neonatal Hypoglycemia”: Mechanism and Implications for Management

The Journal of pediatrics, 2015-06, Vol.166 (6), p.1520-1525.e1

2015

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Surgical treatment of congenital hyperinsulinism: Results from 500 pancreatectomies in neonates and children

Journal of pediatric surgery, 2019-01, Vol.54 (1), p.27-32

2019

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Congenital hyperinsulinism in infancy and childhood: challenges, unmet needs and the perspective of patients and families

Orphanet journal of rare diseases, 2022-02, Vol.17 (1), p.61-12, Article 61

2022

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Novel Presentations of Congenital Hyperinsulinism due to Mutations in the MODY genes: HNF1A and HNF4A

The journal of clinical endocrinology and metabolism, 2012-10, Vol.97 (10), p.E2026-E2030

2012

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GATA6 Plays an Important Role in the Induction of Human Definitive Endoderm, Development of the Pancreas, and Functionality of Pancreatic β Cells

Stem cell reports, 2017-03, Vol.8 (3), p.589-604

2017

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Mosaic GLUD1 Mutations Associated with Hyperinsulinism Hyperammonemia Syndrome

Hormone research in paediatrics, 2022-01, Vol.95 (5), p.492-498

2022

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Correction to: Congenital hyperinsulinism in infancy and childhood: challenges, unmet needs and the perspective of patients and families

Orphanet journal of rare diseases, 2022-05, Vol.17 (1), p.205-205, Article 205

2022

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Characterization of the zebrafish as a model of ATP-sensitive potassium channel hyperinsulinism

BMJ open diabetes research & care, 2024-04, Vol.12 (2), p.e003735

2024

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GLP-1 Receptor Antagonist Exendin-(9-39) Elevates Fasting Blood Glucose Levels in Congenital Hyperinsulinism Owing to Inactivating Mutations in the ATP-Sensitive K+ Channel

Diabetes (New York, N.Y.), 2012-10, Vol.61 (10), p.2585-2591

2012

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New approaches to screening and management of neonatal hypoglycemia based on improved understanding of the molecular mechanism of hypoglycemia

Frontiers in pediatrics, 2023-03, Vol.11, p.1071206-1071206

2023

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Case report: Two unexpected cases of DGUOK-related mitochondrial DNA depletion syndrome presenting with hyperinsulinemic hypoglycemia

Frontiers in endocrinology (Lausanne), 2023-11, Vol.14, p.1268135-1268135

2023

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Congenital Hyperinsulinism in Infants with Turner Syndrome: Possible Association with Monosomy X and KDM6A Haploinsufficiency

Hormone research in paediatrics, 2018-01, Vol.89 (6), p.413-422

2018

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Congenital Hyperinsulinism: A Practical Guide to Diagnosis and Management

1st ed. 2019., 2019

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Congenital hyperinsulinism in children with paternal 11p uniparental isodisomy and Beckwith–Wiedemann syndrome

Journal of medical genetics, 2016-01, Vol.53 (1), p.53-61

2016

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Neonatal Diabetes and Congenital Malabsorptive Diarrhea Attributable to a Novel Mutation in the Human Neurogenin-3 Gene Coding Sequence

The journal of clinical endocrinology and metabolism, 2011-07, Vol.96 (7), p.1960-1965

2011

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Congenital hyperinsulinism disorders: Genetic and clinical characteristics

American journal of medical genetics. Part C, Seminars in medical genetics, 2019-12, Vol.181 (4), p.682-692

2019

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Congenital Hyperinsulinism and Hypopituitarism Attributable to a Mutation in FOXA2

The journal of clinical endocrinology and metabolism, 2018-03, Vol.103 (3), p.1042-1047

2018

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Continuous Glucose Monitoring Systems: Are They Useful for Evaluating Glycemic Control in Children with Hyperinsulinism?

Hormone research in paediatrics, 2019-01, Vol.92 (5), p.319-327

2019

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Recommendations from the Pediatric Endocrine Society for Evaluation and Management of Persistent Hypoglycemia in Neonates, Infants, and Children

Activation of Protein Kinase A (PKA) signaling mitigates congenital hyperinsulinism associated hypoglycemia in the Sur1-/- mouse model

Androgenetic chimerism as an etiology for Beckwith-Wiedemann syndrome: diagnosis and management

The Use of Lanreotide in the Treatment of Congenital Hyperinsulinism

What's in a name? That which we call perinatal stress hyperinsulinism by any other name would smell so bitter

Management and Appropriate Use of Diazoxide in Infants and Children with Hyperinsulinism

The Role of GLP-1 Signaling in Hypoglycemia due to Hyperinsulinism

Re-Evaluating “Transitional Neonatal Hypoglycemia”: Mechanism and Implications for Management

Surgical treatment of congenital hyperinsulinism: Results from 500 pancreatectomies in neonates and children

Congenital hyperinsulinism in infancy and childhood: challenges, unmet needs and the perspective of patients and families

Novel Presentations of Congenital Hyperinsulinism due to Mutations in the MODY genes: HNF1A and HNF4A

GATA6 Plays an Important Role in the Induction of Human Definitive Endoderm, Development of the Pancreas, and Functionality of Pancreatic β Cells

Mosaic GLUD1 Mutations Associated with Hyperinsulinism Hyperammonemia Syndrome

Correction to: Congenital hyperinsulinism in infancy and childhood: challenges, unmet needs and the perspective of patients and families

Characterization of the zebrafish as a model of ATP-sensitive potassium channel hyperinsulinism

GLP-1 Receptor Antagonist Exendin-(9-39) Elevates Fasting Blood Glucose Levels in Congenital Hyperinsulinism Owing to Inactivating Mutations in the ATP-Sensitive K+ Channel

New approaches to screening and management of neonatal hypoglycemia based on improved understanding of the molecular mechanism of hypoglycemia

Case report: Two unexpected cases of DGUOK-related mitochondrial DNA depletion syndrome presenting with hyperinsulinemic hypoglycemia

Congenital Hyperinsulinism in Infants with Turner Syndrome: Possible Association with Monosomy X and KDM6A Haploinsufficiency

Congenital Hyperinsulinism: A Practical Guide to Diagnosis and Management

Congenital hyperinsulinism in children with paternal 11p uniparental isodisomy and Beckwith–Wiedemann syndrome

Neonatal Diabetes and Congenital Malabsorptive Diarrhea Attributable to a Novel Mutation in the Human Neurogenin-3 Gene Coding Sequence

Congenital hyperinsulinism disorders: Genetic and clinical characteristics

Congenital Hyperinsulinism and Hypopituitarism Attributable to a Mutation in FOXA2

Continuous Glucose Monitoring Systems: Are They Useful for Evaluating Glycemic Control in Children with Hyperinsulinism?

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