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Diagnosis, Genetics, and Therapy of Short Stature in Children: A Growth Hormone Research Society International Perspective

Hormone research in paediatrics, 2019, Vol.92 (1), p.1-14

2019

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Maternal-Fetal and Neonatal Endocrinology: Physiology, Pathophysiology, and Clinical Management

1, 2019

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Challenges in the care of individuals with severe primary insulin-like growth factor-I deficiency (SPIGFD): an international, multi-stakeholder perspective

Orphanet journal of rare diseases, 2023-10, Vol.18 (1), p.1-312, Article 312

2023

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Efficacy and Safety of Weekly Somatrogon vs Daily Somatropin in Children With Growth Hormone Deficiency: A Phase 3 Study

The journal of clinical endocrinology and metabolism, 2022-06, Vol.107 (7), p.e2717-e2728

2022

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Growth Hormone Research Society Workshop Summary: Consensus Guidelines for Recombinant Human Growth Hormone Therapy in Prader-Willi Syndrome

The journal of clinical endocrinology and metabolism, 2013-06, Vol.98 (6), p.E1072-E1087

2013

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A Search for Variables Predicting Cortisol Response to Low-Dose Corticotropin Stimulation Following Supraphysiological Doses of Glucocorticoids

The Journal of pediatrics, 2013-08, Vol.163 (2), p.484-488.e1

2013

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Insulin-like Growth Factor 1, but Not Insulin-Like Growth Factor-Binding Protein 3, Predicts Central Precocious Puberty in Girls 6–8 Years Old: A Retrospective Study

Hormone research in paediatrics, 2021-07, Vol.94 (1-2), p.44-51

2021

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Safety Outcomes During Pediatric GH Therapy: Final Results From the Prospective GeNeSIS Observational Program

The journal of clinical endocrinology and metabolism, 2019-02, Vol.104 (2), p.379-389

2019

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The Efficacy, Safety, and Pharmacology of a Ghrelin O-Acyltransferase Inhibitor for the Treatment of Prader-Willi Syndrome

The journal of clinical endocrinology and metabolism, 2022-05, Vol.107 (6), p.e2373-e2380

2022

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Exploring the Association Between DICER1 Mutations and Differentiated Thyroid Carcinoma

The journal of clinical endocrinology and metabolism, 2014-06, Vol.99 (6), p.E1072-E1077

2014

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Clinical Outcomes and Complications of Pituitary Blastoma

The journal of clinical endocrinology and metabolism, 2021-02, Vol.106 (2), p.351-363

2021

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Intranasal Carbetocin Reduces Hyperphagia, Anxiousness, and Distress in Prader-Willi Syndrome: CARE-PWS Phase 3 Trial

The journal of clinical endocrinology and metabolism, 2023-07, Vol.108 (7), p.1696-1708

2023

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Genetic variations at the human growth hormone receptor (GHR) gene locus are associated with idiopathic short stature

Journal of cellular and molecular medicine, 2017-11, Vol.21 (11), p.2985-2999

2017

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Management of phaeochromocytoma and paraganglioma in patients with germline SDHB pathogenic variants: an international expert Consensus statement

Nature reviews. Endocrinology, 2024-03, Vol.20 (3), p.168

2024

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Safety Outcomes and Near-Adult Height Gain of Growth Hormone-Treated Children with SHOX Deficiency: Data from an Observational Study and a Clinical Trial

Hormone research in paediatrics, 2017-01, Vol.87 (1), p.42-50

2017

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Response to: Does IARS2 Deficiency Cause an Intrinsic Disorder of Bone Development (Skeletal Dysplasia) or Are the Reported Skeletal Changes Secondary to Growth Hormone Deficiency and Neuromuscular Involvement?

Human mutation, 2015-03, Vol.36 (3), p.389-389

2015

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Bioinactive ACTH Causing Glucocorticoid Deficiency

The journal of clinical endocrinology and metabolism, 2013-02, Vol.98 (2), p.736-742

2013

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50 years ago in the Journal of Pediatrics: autoimmune disorders of endocrine glands

The Journal of pediatrics, 2013-12, Vol.163 (6), p.1669-1669

2013

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Screening a large pediatric cohort with GH deficiency for mutations in genes regulating pituitary development and GH secretion: Frequencies, phenotypes and growth outcomes

EBioMedicine, 2018-10, Vol.36, p.390-400

2018

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Isosexual precocious pseudopuberty during mitotane treatment in a child with adrenocortical carcinoma: A case report

Pediatric hematology oncology journal, 2024-06, Vol.9 (2), p.74-77

2024

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Genomic Imprinting in Turner Syndrome: Effects on Response to Growth Hormone and on Risk of Sensorineural Hearing Loss

The journal of clinical endocrinology and metabolism, 2006-08, Vol.91 (8), p.3002-3010

2006

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Cortical thickness correlates of socioemotional difficulties in adults with Turner syndrome

Psychoneuroendocrinology, 2014-06, Vol.44, p.30-34

2014

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Abnormal motor cortex excitability is associated with reduced cortical thickness in X monosomy

Human brain mapping, 2013-04, Vol.34 (4), p.936-944

2013

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Diagnosis, Genetics, and Therapy of Short Stature in Children: A Growth Hormone Research Society International Perspective

Maternal-Fetal and Neonatal Endocrinology: Physiology, Pathophysiology, and Clinical Management

Challenges in the care of individuals with severe primary insulin-like growth factor-I deficiency (SPIGFD): an international, multi-stakeholder perspective

Efficacy and Safety of Weekly Somatrogon vs Daily Somatropin in Children With Growth Hormone Deficiency: A Phase 3 Study

Growth Hormone Research Society Workshop Summary: Consensus Guidelines for Recombinant Human Growth Hormone Therapy in Prader-Willi Syndrome

A Search for Variables Predicting Cortisol Response to Low-Dose Corticotropin Stimulation Following Supraphysiological Doses of Glucocorticoids

Insulin-like Growth Factor 1, but Not Insulin-Like Growth Factor-Binding Protein 3, Predicts Central Precocious Puberty in Girls 6–8 Years Old: A Retrospective Study

Safety Outcomes During Pediatric GH Therapy: Final Results From the Prospective GeNeSIS Observational Program

Pituitary blastoma: a pathognomonic feature of germ-line DICER1 mutations

The Efficacy, Safety, and Pharmacology of a Ghrelin O-Acyltransferase Inhibitor for the Treatment of Prader-Willi Syndrome

Exploring the Association Between DICER1 Mutations and Differentiated Thyroid Carcinoma

Clinical Outcomes and Complications of Pituitary Blastoma

Intranasal Carbetocin Reduces Hyperphagia, Anxiousness, and Distress in Prader-Willi Syndrome: CARE-PWS Phase 3 Trial

Genetic variations at the human growth hormone receptor (GHR) gene locus are associated with idiopathic short stature

Management of phaeochromocytoma and paraganglioma in patients with germline SDHB pathogenic variants: an international expert Consensus statement

Mutation in The Nuclear-Encoded Mitochondrial Isoleucyl-tRNA Synthetase IARS2 in Patients with Cataracts, Growth Hormone Deficiency with Short Stature, Partial Sensorineural Deafness, and Peripheral Neuropathy or with Leigh Syndrome

Safety Outcomes and Near-Adult Height Gain of Growth Hormone-Treated Children with SHOX Deficiency: Data from an Observational Study and a Clinical Trial

Response to: Does IARS2 Deficiency Cause an Intrinsic Disorder of Bone Development (Skeletal Dysplasia) or Are the Reported Skeletal Changes Secondary to Growth Hormone Deficiency and Neuromuscular Involvement?

Bioinactive ACTH Causing Glucocorticoid Deficiency

50 years ago in the Journal of Pediatrics: autoimmune disorders of endocrine glands

Screening a large pediatric cohort with GH deficiency for mutations in genes regulating pituitary development and GH secretion: Frequencies, phenotypes and growth outcomes

Isosexual precocious pseudopuberty during mitotane treatment in a child with adrenocortical carcinoma: A case report

Genomic Imprinting in Turner Syndrome: Effects on Response to Growth Hormone and on Risk of Sensorineural Hearing Loss

Cortical thickness correlates of socioemotional difficulties in adults with Turner syndrome

Abnormal motor cortex excitability is associated with reduced cortical thickness in X monosomy

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