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Endocrine Disorders in Children with Brain Tumors: At Diagnosis, after Surgery, Radiotherapy and Chemotherapy

Children (Basel), 2022-10, Vol.9 (11), p.1617

2022

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Risk of thyroid neoplasms in patients with 22q11.2 deletion and DiGeorge-like syndromes: an insight for follow-up

Frontiers in endocrinology (Lausanne), 2023-08, Vol.14, p.1209577-1209577

2023

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Homozygous HESX1 and COL1A1 Gene Variants in a Boy with Growth Hormone Deficiency and Early Onset Osteoporosis

International journal of molecular sciences, 2021-01, Vol.22 (2), p.750

2021

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Relationship of CYP21A2 genotype and serum 17-hydroxyprogesterone and cortisol levels in a large cohort of Italian children with premature pubarche

European journal of endocrinology, 2011-08, Vol.165 (2), p.307-314

2011

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Bone and body composition analyzed by Dual-energy X-ray Absorptiometry (DXA) in clinical and nutritional evaluation of young patients with Cystic Fibrosis: a cross-sectional study

BMC pediatrics, 2009-09, Vol.9 (1), p.61-61, Article 61

2009

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Partially Reversible Hypopituitarism in an Adolescent with a Rathke Cleft Cyst

Clinical Pediatric Endocrinology, 2012, Vol.21(4), pp.75-80

2012

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Partially Reversible Hypopituitarism in an Adolescent with a Rathke Cleft Cyst

Clinical Pediatric Endocrinology, 2012-10, Vol.21 (4), p.75-80

2012

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Noonan Syndrome Growth Charts and Genotypes: 15-Year Longitudinal Single-Centre Study

Hormone research in paediatrics, 2024-07, p.1-13

2024

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Towards an individualized management of pubertal induction in girls with hypogonadism: insight into the best replacement outcomes from a large multicentre registry

European journal of endocrinology, 2023-06, Vol.188 (6), p.467-476

2023

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Thyroid carcinoma in two patients with ataxia‐telangiectasia: Tailored diagnostic and therapeutic use of radioiodine

Pediatric blood & cancer, 2023-10, Vol.70 (10), p.e30535-n/a

2023

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Management of Childhood-onset Craniopharyngioma in Italy: A Multicenter, 7-Year Follow-up Study of 145 Patients

The journal of clinical endocrinology and metabolism, 2022-02, Vol.107 (3), p.e1020-e1031

2022

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Nocturnal hypoglycaemia in ACTH and GH deficient children: role of continuous glucose monitoring

Clinical endocrinology (Oxford), 2013-08, Vol.79 (2), p.232-237

2013

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Polycystic ovary syndrome in pediatric obesity and diabetes

Minerva Pediatrics, 2021-12, Vol.73 (6), p.523

2021

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Usefulness of iodine-123 whole-body scan in planning iodine-131 treatment of the differentiated thyroid carcinoma in children and adolescence

Nuclear medicine communications, 2018-12, Vol.39 (12), p.1121-1128

2018

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Epidemiology, Presentation and Long-Term Evolution of Graves' Disease in Children, Adolescents and Young Adults with Turner Syndrome

Hormone research in paediatrics, 2014-01, Vol.81 (4), p.245-250

2014

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Efficacy and safety of growth hormone treatment in children with short stature: the Italian cohort of the GeNeSIS clinical study

Journal of endocrinological investigation, 2016-06, Vol.39 (6), p.667-677

2016

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Obese Children with Low Birth Weight Demonstrate Impaired β-Cell Function during Oral Glucose Tolerance Test

The journal of clinical endocrinology and metabolism, 2009-11, Vol.94 (11), p.4448-4452

2009

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Smart-web support: a new tool to help information sharing in managing complex paediatric diseases. Study protocol.

Recenti progressi in medicina, 2016-11, Vol.107 (11), p.586

2016

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Non-conventional use of growth hormone therapy

Acta pædiatrica (Oslo), 2006-07, Vol.95, p.9-13

2006

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Cardiovascular fitness, insulin resistance and metabolic syndrome in severely obese prepubertal Italian children

Hormone research, 2008-01, Vol.70 (6), p.349-356

2008

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Bone and body composition analyzed by Dual-energy X-ray Absorptiometry

BMC pediatrics, 2009-09, Vol.9, p.61

2009

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Non-conventional use of growth hormone therapy

Acta Paediatrica, 2006-07, Vol.95 (S452), p.9-13

2006

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Blood Pressure and Left Ventricular Characteristics in Young Patients with Classical Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency

International journal of pediatric endocrinology, 2009, Vol.2009, p.1-6

2009

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Deletion of chromosome 1q24-1q32 and combined pituitary hormone deficiency type 4: Insight into the challenges of genotype-phenotype correlation

Endocrine Abstracts, 2020-08

2020

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Pubertal induction in girls with hypogonadism: insight into estrogen replacement therapy outcomes and optimization of progesterone introduction

Endocrine Abstracts, 2022-05

2022

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Endocrine Disorders in Children with Brain Tumors: At Diagnosis, after Surgery, Radiotherapy and Chemotherapy

Risk of thyroid neoplasms in patients with 22q11.2 deletion and DiGeorge-like syndromes: an insight for follow-up

Homozygous HESX1 and COL1A1 Gene Variants in a Boy with Growth Hormone Deficiency and Early Onset Osteoporosis

Relationship of CYP21A2 genotype and serum 17-hydroxyprogesterone and cortisol levels in a large cohort of Italian children with premature pubarche

Bone and body composition analyzed by Dual-energy X-ray Absorptiometry (DXA) in clinical and nutritional evaluation of young patients with Cystic Fibrosis: a cross-sectional study

Partially Reversible Hypopituitarism in an Adolescent with a Rathke Cleft Cyst

Partially Reversible Hypopituitarism in an Adolescent with a Rathke Cleft Cyst

Noonan Syndrome Growth Charts and Genotypes: 15-Year Longitudinal Single-Centre Study

Towards an individualized management of pubertal induction in girls with hypogonadism: insight into the best replacement outcomes from a large multicentre registry

Thyroid carcinoma in two patients with ataxia‐telangiectasia: Tailored diagnostic and therapeutic use of radioiodine

Management of Childhood-onset Craniopharyngioma in Italy: A Multicenter, 7-Year Follow-up Study of 145 Patients

Nocturnal hypoglycaemia in ACTH and GH deficient children: role of continuous glucose monitoring

Polycystic ovary syndrome in pediatric obesity and diabetes

Usefulness of iodine-123 whole-body scan in planning iodine-131 treatment of the differentiated thyroid carcinoma in children and adolescence

Epidemiology, Presentation and Long-Term Evolution of Graves' Disease in Children, Adolescents and Young Adults with Turner Syndrome

Efficacy and safety of growth hormone treatment in children with short stature: the Italian cohort of the GeNeSIS clinical study

Obese Children with Low Birth Weight Demonstrate Impaired β-Cell Function during Oral Glucose Tolerance Test

Smart-web support: a new tool to help information sharing in managing complex paediatric diseases. Study protocol.

Non-conventional use of growth hormone therapy

Cardiovascular fitness, insulin resistance and metabolic syndrome in severely obese prepubertal Italian children

Bone and body composition analyzed by Dual-energy X-ray Absorptiometry

Non-conventional use of growth hormone therapy

Blood Pressure and Left Ventricular Characteristics in Young Patients with Classical Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency

Deletion of chromosome 1q24-1q32 and combined pituitary hormone deficiency type 4: Insight into the challenges of genotype-phenotype correlation

Pubertal induction in girls with hypogonadism: insight into estrogen replacement therapy outcomes and optimization of progesterone introduction

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