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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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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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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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Visual interpretation, not SUV ratios, is the ideal method to interpret 18F-DOPA PET scans to aid in the cure of patients with focal congenital hyperinsulinism

PloS one, 2020-10, Vol.15 (10), p.e0241243

2020

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Neonates at risk for hypoglycemia: associated neurological outcomes

The Journal of pediatrics, 2016-03, Vol.170, p.341-344

Thornton, Paul S., MB, BCh

2016

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Hyperinsulinemic Hypoglycemia Associated with a CaV1.2 Variant with Mixed Gain- and Loss-of-Function Effects

International journal of molecular sciences, 2022-07, Vol.23 (15), p.8097

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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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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Pancreatic uptake and radiation dosimetry of 6-[18F]fluoro-L-DOPA from PET imaging studies in infants with congenital hyperinsulinism

PloS one, 2017-11, Vol.12 (11), p.e0186340

2017

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Approach to the Patient: Investigation of pediatric hypoglycemia in the emergency department - a practical algorithm

The journal of clinical endocrinology and metabolism, 2024-02, Vol.109 (7), p.e1513-e1521

2024

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Weekly Lonapegsomatropin in Treatment-Naïve Children With Growth Hormone Deficiency: The Phase 3 heiGHt Trial

The journal of clinical endocrinology and metabolism, 2021-11, Vol.106 (11), p.3184-3195

2021

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Familial Hyperinsulinism Caused by an Activating Glucokinase Mutation

The New England journal of medicine, 1998-01, Vol.338 (4), p.226-230

1998

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Dasiglucagon for the Treatment of Congenital Hyperinsulinism: A Randomized Phase 3 Trial in Infants and Children

The journal of clinical endocrinology and metabolism, 2024-03, Vol.109 (4), p.1071-1079

2024

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Clinical and Molecular Characterization of a Dominant Form of Congenital Hyperinsulinism Caused by a Mutation in the High-Affinity Sulfonylurea Receptor

Diabetes (New York, N.Y.), 2003-09, Vol.52 (9), p.2403-2410

2003

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The GLOW Study does not light up the true Pediatric Endocrine Society recommendations for management of hypoglycemia in newborns

The Journal of pediatrics, 2020-10, Vol.225, p.279-279

2020

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Congenital Hyperinsulinism: An Historical Perspective

Hormone research in paediatrics, 2022, Vol.95 (6), p.631-637

2022

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

Journal of pediatric surgery, 2004-03, Vol.39 (3), p.270-275

2004

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The Incidence and Etiology of Previously Undiagnosed Hypoglycemic Disorders in the Emergency Department

Pediatric emergency care, 2020-07, Vol.36 (7), p.322

2020

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Safety and Efficacy of Lonapegsomatropin in Children With Growth Hormone Deficiency: enliGHten Trial 2-Year Results

The journal of clinical endocrinology and metabolism, 2022-06, Vol.107 (7), p.e2680-e2689

2022

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Response to Letter to the Editor From L. Sävendahl et al: "Weekly Lonapegsomatropin in Treatment-Naïve Children With Growth Hormone Deficiency: The Phase 3 heiGHt Trial"

The journal of clinical endocrinology and metabolism, 2022-02, Vol.107 (3), p.e1333-e1334

2022

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Response to Letter to the Editor From Malozowski: "Weekly Lonapegsomatropin in Treatment-Naïve Children With Growth Hormone Deficiency: The Phase 3 heiGHt Trial"

The journal of clinical endocrinology and metabolism, 2022-04, Vol.107 (5), p.e2215-e2216

2022

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International Guidelines for the Diagnosis and Management of Hyperinsulinism

Hormone research in paediatrics, 2023-07, Vol.97 (3), p.279-298

2023

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PRACTICE VARIATION IN THE MANAGEMENT OF GIRLS AND BOYS WITH DELAYED PUBERTY

Endocrine practice, 2020-03, Vol.26 (3), p.267-284

2020

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Treatment Threshold for Neonatal Hypoglycemia

The New England journal of medicine, 2020-06, Vol.382 (23), p.2272-2274

2020

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Switching to Weekly Lonapegsomatropin from Daily Somatropin in Children with Growth Hormone Deficiency: The fliGHt Trial

Hormone research in paediatrics, 2022-08, Vol.95 (3), p.233-243

2022

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

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

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

Visual interpretation, not SUV ratios, is the ideal method to interpret 18F-DOPA PET scans to aid in the cure of patients with focal congenital hyperinsulinism

Neonates at risk for hypoglycemia: associated neurological outcomes

Hyperinsulinemic Hypoglycemia Associated with a CaV1.2 Variant with Mixed Gain- and Loss-of-Function Effects

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

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

Pancreatic uptake and radiation dosimetry of 6-[18F]fluoro-L-DOPA from PET imaging studies in infants with congenital hyperinsulinism

Approach to the Patient: Investigation of pediatric hypoglycemia in the emergency department - a practical algorithm

Weekly Lonapegsomatropin in Treatment-Naïve Children With Growth Hormone Deficiency: The Phase 3 heiGHt Trial

Familial Hyperinsulinism Caused by an Activating Glucokinase Mutation

Dasiglucagon for the Treatment of Congenital Hyperinsulinism: A Randomized Phase 3 Trial in Infants and Children

Clinical and Molecular Characterization of a Dominant Form of Congenital Hyperinsulinism Caused by a Mutation in the High-Affinity Sulfonylurea Receptor

The GLOW Study does not light up the true Pediatric Endocrine Society recommendations for management of hypoglycemia in newborns

Congenital Hyperinsulinism: An Historical Perspective

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

The Incidence and Etiology of Previously Undiagnosed Hypoglycemic Disorders in the Emergency Department

Safety and Efficacy of Lonapegsomatropin in Children With Growth Hormone Deficiency: enliGHten Trial 2-Year Results

Response to Letter to the Editor From L. Sävendahl et al: "Weekly Lonapegsomatropin in Treatment-Naïve Children With Growth Hormone Deficiency: The Phase 3 heiGHt Trial"

Response to Letter to the Editor From Malozowski: "Weekly Lonapegsomatropin in Treatment-Naïve Children With Growth Hormone Deficiency: The Phase 3 heiGHt Trial"

International Guidelines for the Diagnosis and Management of Hyperinsulinism

PRACTICE VARIATION IN THE MANAGEMENT OF GIRLS AND BOYS WITH DELAYED PUBERTY

Treatment Threshold for Neonatal Hypoglycemia

Switching to Weekly Lonapegsomatropin from Daily Somatropin in Children with Growth Hormone Deficiency: The fliGHt Trial

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