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46,XX DSD due to Androgen Excess in Monogenic Disorders of Steroidogenesis: Genetic, Biochemical, and Clinical Features

International journal of molecular sciences, 2019-09, Vol.20 (18), p.4605

2019

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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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Auxological and endocrine findings in narcolepsy type 1: seventeen-year follow-up from a pediatric endocrinology center

Frontiers in endocrinology (Lausanne), 2023-06, Vol.14, p.1037398-1037398

2023

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Normative Basal Values of Hormones and Proteins of Gonadal and Adrenal Functions from Birth to Adulthood

Sexual development, 2018-01, Vol.12 (1-3), p.50-94

2018

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Comparison between Liquid and Tablet Formulations of Levothyroxine in the Initial Treatment of Congenital Hypothyroidism

The Journal of pediatrics, 2013-06, Vol.162 (6), p.1264-1269.e2

2013

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Premature Pubarche: Time to Revise the Diagnostic Approach?

Journal of clinical medicine, 2023-03, Vol.12 (6), p.2187

2023

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Congenital Adrenal Hyperplasias Presenting in the Newborn and Young Infant

Frontiers in pediatrics, 2020-12, Vol.8, p.593315-593315

2020

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Testicular Adrenal Rest Tumors in Congenital Adrenal Hyperplasia: Study of a Cohort of Patients from a Single Italian Center

Children (Basel), 2023-08, Vol.10 (9), p.1457

2023

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Severe obesity and cardiometabolic risk in children: comparison from two international classification systems

PloS one, 2013-12, Vol.8 (12), p.e83793-e83793

2013

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Characterization of deletions at 9p affecting the candidate regions for sex reversal and deletion 9p syndrome by MLPA

European journal of human genetics : EJHG, 2009-11, Vol.17 (11), p.1439-1447

2009

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Friction Forces during Sliding of Various Brackets for Malaligned Teeth: An In Vitro Study

TheScientificWorld, 2013-01, Vol.2013 (1), p.871423

2013

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The delocalisation of mafia organisations and the construction of a European law against organised crime

Global crime, 2016-01, Vol.17 (1), p.99-121

Balsamo, Antonio

2016

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CYP21 Genotype, Adult Height, and Pubertal Development in 55 Patients Treated for 21-Hydroxylase Deficiency

The journal of clinical endocrinology and metabolism, 2003-12, Vol.88 (12), p.5680-5688

2003

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Growing Up with Type 1 Narcolepsy: Its Anthropometric and Endocrine Features

Journal of clinical sleep medicine, 2016-12, Vol.12 (12), p.1649-1657

2016

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Italian cross-sectional growth charts for height, weight and BMI (2 to 20 yr)

Journal of endocrinological investigation, 2006-07, Vol.29 (7), p.581-593

2006

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High prevalence of precocious puberty and obesity in childhood narcolepsy with cataplexy

Sleep (New York, N.Y.), 2013-02, Vol.36 (2), p.175-181

2013

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Prevalence of pathogenetic MC4R mutations in Italian children with early onset obesity, tall stature and familial history of obesity

BMC medical genetics, 2009-03, Vol.10 (1), p.25-25, Article 25

2009

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Changes over time in sex assignment for disorders of sex development

Pediatrics (Evanston), 2014-09, Vol.134 (3), p.e710

2014

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Mutational and functional studies on NR5A1 gene in 46,XY disorders of sex development: identification of six novel loss of function mutations

Fertility and sterility, 2018-06, Vol.109 (6), p.1105-1113

2018

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Real-World Estimates of Adrenal Insufficiency–Related Adverse Events in Children With Congenital Adrenal Hyperplasia

The journal of clinical endocrinology and metabolism, 2021-01, Vol.106 (1), p.e192-e203

2021

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Comment on “Complete Androgen Insensitivity Syndrome: Optimizing Diagnosis and Management”

Case reports in obstetrics and gynecology, 2014-01, Vol.2014, p.285715-3

2014

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Functional characterization of naturally occurring NR3C2 gene mutations in Italian patients suffering from pseudohypoaldosteronism type 1

European journal of endocrinology, 2007-02, Vol.156 (2), p.249

2007

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Birth length and weight in congenital adrenal hyperplasia according to the different phenotypes

European journal of pediatrics, 2006-06, Vol.165 (6), p.380-383

2006

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Diagnosis, treatment and prevention of pediatric obesity: consensus position statement of the Italian Society for Pediatric Endocrinology and Diabetology and the Italian Society of Pediatrics

Italian journal of pediatrics, 2018-07, Vol.44 (1), p.88-88, Article 88

2018

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46,XX DSD due to Androgen Excess in Monogenic Disorders of Steroidogenesis: Genetic, Biochemical, and Clinical Features

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

Auxological and endocrine findings in narcolepsy type 1: seventeen-year follow-up from a pediatric endocrinology center

Treatment of congenital adrenal hyperplasia in children aged 0-3 years: a retrospective multicenter analysis of salt supplementation, glucocorticoid and mineralocorticoid medication, growth and blood pressure

Normative Basal Values of Hormones and Proteins of Gonadal and Adrenal Functions from Birth to Adulthood

Comparison between Liquid and Tablet Formulations of Levothyroxine in the Initial Treatment of Congenital Hypothyroidism

Premature Pubarche: Time to Revise the Diagnostic Approach?

Congenital Adrenal Hyperplasias Presenting in the Newborn and Young Infant

Testicular Adrenal Rest Tumors in Congenital Adrenal Hyperplasia: Study of a Cohort of Patients from a Single Italian Center

Severe obesity and cardiometabolic risk in children: comparison from two international classification systems

Characterization of deletions at 9p affecting the candidate regions for sex reversal and deletion 9p syndrome by MLPA

Friction Forces during Sliding of Various Brackets for Malaligned Teeth: An In Vitro Study

The delocalisation of mafia organisations and the construction of a European law against organised crime

CYP21 Genotype, Adult Height, and Pubertal Development in 55 Patients Treated for 21-Hydroxylase Deficiency

Growing Up with Type 1 Narcolepsy: Its Anthropometric and Endocrine Features

Italian cross-sectional growth charts for height, weight and BMI (2 to 20 yr)

High prevalence of precocious puberty and obesity in childhood narcolepsy with cataplexy

Prevalence of pathogenetic MC4R mutations in Italian children with early onset obesity, tall stature and familial history of obesity

Changes over time in sex assignment for disorders of sex development

Mutational and functional studies on NR5A1 gene in 46,XY disorders of sex development: identification of six novel loss of function mutations

Real-World Estimates of Adrenal Insufficiency–Related Adverse Events in Children With Congenital Adrenal Hyperplasia

Comment on “Complete Androgen Insensitivity Syndrome: Optimizing Diagnosis and Management”

Functional characterization of naturally occurring NR3C2 gene mutations in Italian patients suffering from pseudohypoaldosteronism type 1

Birth length and weight in congenital adrenal hyperplasia according to the different phenotypes

Diagnosis, treatment and prevention of pediatric obesity: consensus position statement of the Italian Society for Pediatric Endocrinology and Diabetology and the Italian Society of Pediatrics

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