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Advances in differential diagnosis and management of growth hormone deficiency in children

Nature reviews. Endocrinology, 2021-10, Vol.17 (10), p.608

2021

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Gut-microbiota in children and adolescents with obesity: inferred functional analysis and machine-learning algorithms to classify microorganisms

Scientific reports, 2023-07, Vol.13 (1), p.11294-11294, Article 11294

2023

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Wolfram syndrome 1 in the Italian population: genotype-phenotype correlations

Pediatric research, 2020-02, Vol.87 (3), p.456-462

2020

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Primary Adrenal Insufficiency in Childhood: Data From a Large Nationwide Cohort

The journal of clinical endocrinology and metabolism, 2021-03, Vol.106 (3), p.762-773

2021

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Infectious diseases associated with pediatric type 1 diabetes mellitus: A narrative review

Frontiers in endocrinology (Lausanne), 2022-08, Vol.13, p.966344-966344

2022

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Abnormalities of pubertal development and gonadal function in Noonan syndrome

Frontiers in endocrinology (Lausanne), 2023-07, Vol.14, p.1213098-1213098

2023

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The Italian registry for patients with Prader-Willi syndrome

Orphanet journal of rare diseases, 2023-02, Vol.18 (1), p.28-28, Article 28

2023

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Characterization of Two Novel Variants of the Steroidogenic Acute Regulatory Protein Identified in a Girl with Classic Lipoid Congenital Adrenal Hyperplasia

International journal of molecular sciences, 2020-08, Vol.21 (17), p.6185

2020

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Growth in Children With Noonan Syndrome and Effects of Growth Hormone Treatment on Adult Height

Frontiers in endocrinology (Lausanne), 2021-12, Vol.12, p.761171-761171

2021

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Pubertal timing in children with Silver Russell syndrome compared to those born small for gestational age

Frontiers in endocrinology (Lausanne), 2022-08, Vol.13, p.975511-975511

2022

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Corrigendum: Pubertal timing in children with Silver Russell syndrome compared to those born small for gestational age

Frontiers in endocrinology (Lausanne), 2023-03, Vol.14, p.1172736-1172736

2023

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Maternal Uniparental Disomy of Chromosome 20 (UPD(20)mat) as Differential Diagnosis of Silver Russell Syndrome: Identification of Three New Cases

Genes, 2021-04, Vol.12 (4), p.588

2021

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IGF1 for the diagnosis of growth hormone deficiency in children and adolescents: a reappraisal

Endocrine Connections, 2020-11, Vol.9 (11), p.1095-1102

2020

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Letter to the Editor: "Forty-One Individuals With Mutations in the AVP-NPII Gene Associated With Familial Neurohypophyseal Diabetes Insipidus."

The journal of clinical endocrinology and metabolism, 2020-07, Vol.105 (7), p.e2675-e2676

2020

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Antibodies Against Hypothalamus and Pituitary Gland in Childhood-Onset Brain Tumors and Pituitary Dysfunction

Frontiers in endocrinology (Lausanne), 2020-02, Vol.11, p.16-16

2020

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A case report of glucose transporter 1 deficiency syndrome with growth hormone deficiency diagnosed before starting ketogenic diet

Italian journal of pediatrics, 2020-08, Vol.46 (1), p.1-119, Article 119

2020

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Accuracy and Limitations of the Growth Hormone (GH) Releasing Hormone-Arginine Retesting in Young Adults With Childhood-Onset GH Deficiency

Frontiers in endocrinology (Lausanne), 2019-07, Vol.10, p.525-525

2019

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Update on bone density measurements and their interpretation in children and adolescents

Baillière's best practice & research. Clinical endocrinology & metabolism, 2018-08, Vol.32 (4), p.477-498

2018

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Approach to the Pediatric Patient: Central Diabetes Insipidus

The journal of clinical endocrinology and metabolism, 2022-04, Vol.107 (5), p.1407-1416

2022

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Central diabetes insipidus in children: Diagnosis and management

Baillière's best practice & research. Clinical endocrinology & metabolism, 2020-09, Vol.34 (5), p.101440, Article 101440

2020

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Sleep disorders in Prader-Willi syndrome, evidence from animal models and humans

Sleep medicine reviews, 2021-06, Vol.57, p.101432-101432, Article 101432

2021

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Gut Microbiota in T1DM-Onset Pediatric Patients: Machine-Learning Algorithms to Classify Microorganisms as Disease Linked

The journal of clinical endocrinology and metabolism, 2020-09, Vol.105 (9), p.e3114-e3126

2020

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Accuracy of Glucagon Testing Across Transition in Young Adults With Childhood-Onset GH Deficiency

The journal of clinical endocrinology and metabolism, 2024-06

2024

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Central adrenal insufficiency in children and adolescents

Baillière's best practice & research. Clinical endocrinology & metabolism, 2018-08, Vol.32 (4), p.425-444

2018

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Sirolimus Therapy in Congenital Hyperinsulinism: A Successful Experience Beyond Infancy

Pediatrics (Evanston), 2015-11, Vol.136 (5), p.e1373

2015

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Advances in differential diagnosis and management of growth hormone deficiency in children

Gut-microbiota in children and adolescents with obesity: inferred functional analysis and machine-learning algorithms to classify microorganisms

Wolfram syndrome 1 in the Italian population: genotype-phenotype correlations

Primary Adrenal Insufficiency in Childhood: Data From a Large Nationwide Cohort

Infectious diseases associated with pediatric type 1 diabetes mellitus: A narrative review

Abnormalities of pubertal development and gonadal function in Noonan syndrome

The Italian registry for patients with Prader-Willi syndrome

Characterization of Two Novel Variants of the Steroidogenic Acute Regulatory Protein Identified in a Girl with Classic Lipoid Congenital Adrenal Hyperplasia

Growth in Children With Noonan Syndrome and Effects of Growth Hormone Treatment on Adult Height

Pubertal timing in children with Silver Russell syndrome compared to those born small for gestational age

Corrigendum: Pubertal timing in children with Silver Russell syndrome compared to those born small for gestational age

Maternal Uniparental Disomy of Chromosome 20 (UPD(20)mat) as Differential Diagnosis of Silver Russell Syndrome: Identification of Three New Cases

IGF1 for the diagnosis of growth hormone deficiency in children and adolescents: a reappraisal

Letter to the Editor: "Forty-One Individuals With Mutations in the AVP-NPII Gene Associated With Familial Neurohypophyseal Diabetes Insipidus."

Antibodies Against Hypothalamus and Pituitary Gland in Childhood-Onset Brain Tumors and Pituitary Dysfunction

A case report of glucose transporter 1 deficiency syndrome with growth hormone deficiency diagnosed before starting ketogenic diet

Accuracy and Limitations of the Growth Hormone (GH) Releasing Hormone-Arginine Retesting in Young Adults With Childhood-Onset GH Deficiency

Update on bone density measurements and their interpretation in children and adolescents

Approach to the Pediatric Patient: Central Diabetes Insipidus

Central diabetes insipidus in children: Diagnosis and management

Sleep disorders in Prader-Willi syndrome, evidence from animal models and humans

Gut Microbiota in T1DM-Onset Pediatric Patients: Machine-Learning Algorithms to Classify Microorganisms as Disease Linked

Accuracy of Glucagon Testing Across Transition in Young Adults With Childhood-Onset GH Deficiency

Central adrenal insufficiency in children and adolescents

Sirolimus Therapy in Congenital Hyperinsulinism: A Successful Experience Beyond Infancy

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