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Ontogeny of Hypothalamus-Pituitary Gonadal Axis and Minipuberty: An Ongoing Debate?

Frontiers in endocrinology (Lausanne), 2020-04, Vol.11, p.187-187

2020

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X-linked adrenoleukodystrophy and primary adrenal insufficiency

Frontiers in endocrinology (Lausanne), 2023-11, Vol.14, p.1309053-1309053

2023

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"Impact of COVID-19 pandemic lockdown on early onset of puberty: experience of an Italian tertiary center"

Italian journal of pediatrics, 2021-03, Vol.47 (1), p.52-52, Article 52

2021

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The Bones of Children With Obesity

Frontiers in endocrinology (Lausanne), 2020-04, Vol.11, p.200-200

2020

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Analysis of the AIRE Gene Promoter in Patients Affected by Autoimmune Polyendocrine Syndromes

International journal of molecular sciences, 2024-03, Vol.25 (5), p.2656

2024

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Sedentary lifestyle and precocious puberty in girls during the COVID-19 pandemic: an Italian experience

Endocrine Connections, 2022-02, Vol.11 (2), p.1-10

2022

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COVID-19 pandemic phases and female precocious puberty: The experience of the past 4 years (2019 through 2022) in an Italian tertiary center

Frontiers in endocrinology (Lausanne), 2023-02, Vol.14, p.1132769-1132769

2023

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Low Levels of Serum Total Vitamin B12 Are Associated with Worse Metabolic Phenotype in a Large Population of Children, Adolescents and Young Adults, from Underweight to Severe Obesity

International journal of molecular sciences, 2023-12, Vol.24 (23), p.16588

2023

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Adrenal crisis in infants and young children with adrenal insufficiency: Management and prevention

Frontiers in endocrinology (Lausanne), 2023-02, Vol.14, p.1133376-1133376

2023

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Insulin Clearance at the Pubertal Transition in Youth with Obesity and Steatosis Liver Disease

International journal of molecular sciences, 2023-10, Vol.24 (19), p.14963

2023

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Effect of p53 activation through targeting MDM2/MDM4 heterodimer on T regulatory and effector cells in the peripheral blood of Type 1 diabetes patients

PloS one, 2020-01, Vol.15 (1), p.e0228296-e0228296

2020

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A rare occurrence of non-classic congenital adrenal hyperplasia and type 1 diabetes mellitus in a girl with Prader-Willi Syndrome: Case report and review of the literature

Frontiers in endocrinology (Lausanne), 2023-04, Vol.14, p.1148318-1148318

2023

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Low Birthweight Increases the Likelihood of Severe Steatosis in Pediatric Non-Alcoholic Fatty Liver Disease

The American journal of gastroenterology, 2017-08, Vol.112 (8), p.1277-1286

2017

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Biallelic Inactivating TUB Variants Cause Retinal Ciliopathy Impairing Biogenesis and the Structure of the Primary Cilium

International journal of molecular sciences, 2022-12, Vol.23 (23), p.14656

2022

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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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Case report: Long term response to growth hormone in a child with Silver-Russell syndrome-like phenotype due to a novel paternally inherited IGF2 variant

Frontiers in endocrinology (Lausanne), 2024-03, Vol.15, p.1364234

2024

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Use of GLP-1 receptor agonists in Prader-Willi Syndrome: report of six cases

Diabetes care, 2014-04, Vol.37 (4), p.e76-e77

2014

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Water Balance and ‘Salt Wasting' in the First Year of Life: The Role of Aldosterone-Signaling Defects

Hormone research in paediatrics, 2016-01, Vol.86 (3), p.143-153

2016

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Expression of PD-1 Molecule on Regulatory T Lymphocytes in Patients with Insulin-Dependent Diabetes Mellitus

International journal of molecular sciences, 2015-09, Vol.16 (9), p.22584-22605

2015

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Analysis of a series of Italian APECED patients with autoimmune hepatitis and gastro-enteropathies

Frontiers in immunology, 2023-06, Vol.14, p.1172369-1172369

2023

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Metreleptin for the treatment of progressive encephalopathy with/without lipodystrophy (PELD) in a child with progressive myoclonic epilepsy: a case report

Italian journal of pediatrics, 2020-10, Vol.46 (1), p.158-158, Article 158

2020

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Case report: Management of pediatric gigantism caused by the TADopathy, X-linked acrogigantism

Frontiers in endocrinology (Lausanne), 2024-02, Vol.15, p.1345363

2024

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Mutations in the NHEJ Component XRCC4 Cause Primordial Dwarfism

American journal of human genetics, 2015-03, Vol.96 (3), p.412-424

2015

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Identification of GAD65 AA 114-122 reactive 'memory-like' NK cells in newly diagnosed Type 1 diabetic patients by HLA-class I pentamers

PloS one, 2017-12, Vol.12 (12), p.e0189615-e0189615

2017

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Autoimmune Thyroid Diseases in Children

Journal of Thyroid Research, 2011-01, Vol.2011, p.675703-13

2011

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Ontogeny of Hypothalamus-Pituitary Gonadal Axis and Minipuberty: An Ongoing Debate?

X-linked adrenoleukodystrophy and primary adrenal insufficiency

"Impact of COVID-19 pandemic lockdown on early onset of puberty: experience of an Italian tertiary center"

The Bones of Children With Obesity

Analysis of the AIRE Gene Promoter in Patients Affected by Autoimmune Polyendocrine Syndromes

Sedentary lifestyle and precocious puberty in girls during the COVID-19 pandemic: an Italian experience

COVID-19 pandemic phases and female precocious puberty: The experience of the past 4 years (2019 through 2022) in an Italian tertiary center

Low Levels of Serum Total Vitamin B12 Are Associated with Worse Metabolic Phenotype in a Large Population of Children, Adolescents and Young Adults, from Underweight to Severe Obesity

Adrenal crisis in infants and young children with adrenal insufficiency: Management and prevention

Insulin Clearance at the Pubertal Transition in Youth with Obesity and Steatosis Liver Disease

Effect of p53 activation through targeting MDM2/MDM4 heterodimer on T regulatory and effector cells in the peripheral blood of Type 1 diabetes patients

A rare occurrence of non-classic congenital adrenal hyperplasia and type 1 diabetes mellitus in a girl with Prader-Willi Syndrome: Case report and review of the literature

Low Birthweight Increases the Likelihood of Severe Steatosis in Pediatric Non-Alcoholic Fatty Liver Disease

Biallelic Inactivating TUB Variants Cause Retinal Ciliopathy Impairing Biogenesis and the Structure of the Primary Cilium

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

Case report: Long term response to growth hormone in a child with Silver-Russell syndrome-like phenotype due to a novel paternally inherited IGF2 variant

Use of GLP-1 receptor agonists in Prader-Willi Syndrome: report of six cases

Water Balance and ‘Salt Wasting' in the First Year of Life: The Role of Aldosterone-Signaling Defects

Expression of PD-1 Molecule on Regulatory T Lymphocytes in Patients with Insulin-Dependent Diabetes Mellitus

Analysis of a series of Italian APECED patients with autoimmune hepatitis and gastro-enteropathies

Metreleptin for the treatment of progressive encephalopathy with/without lipodystrophy (PELD) in a child with progressive myoclonic epilepsy: a case report

Case report: Management of pediatric gigantism caused by the TADopathy, X-linked acrogigantism

Mutations in the NHEJ Component XRCC4 Cause Primordial Dwarfism

Identification of GAD65 AA 114-122 reactive 'memory-like' NK cells in newly diagnosed Type 1 diabetic patients by HLA-class I pentamers

Autoimmune Thyroid Diseases in Children

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