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Impaired Growth during Childhood in Patients with Primary Ciliary Dyskinesia

International Journal of Endocrinology, 2013-01, Vol.2013, p.731423-5

2013

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Update on Age at Menarche in Italy: Toward the Leveling Off of the Secular Trend

Journal of adolescent health, 2010-03, Vol.46 (3), p.238-244

2010

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Menstrual pattern and menstrual disorders among adolescents: an update of the Italian data

Italian journal of pediatrics, 2012-08, Vol.38 (1), p.38-38, Article 38

2012

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The levelling-off of the secular trend of age at menarche among Italian girls

Heliyon, 2020-06, Vol.6 (6), p.e04222-e04222, Article e04222

2020

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Transient Neonatal Zinc Deficiency Caused by a Heterozygous G87R Mutation in the Zinc Transporter ZnT-2 (SLC30A2) Gene in the Mother Highlighting the Importance of Zn2+ for Normal Growth and Development

International journal of endocrinology, 2013-01, Vol.2013

2013

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Onset of menstrual cycle and menses features among secondary school girls in Italy: A questionnaire study on 3,783 students

Indian journal of endocrinology and metabolism, 2014-11, Vol.18 (Suppl 1), p.S84-S92

2014

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Early onset of puberty during COVID-19 pandemic lockdown: experience from two Pediatric Endocrinology Italian Centers

Journal of pediatric endocrinology & metabolism : JPEM, 2023-03, Vol.36 (3), p.290

2023

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Primary Dysmenorrhea in Adolescents: Prevalence, Impact and Recent Knowledge

Pediatric endocrinology reviews : PER, 2015-12, Vol.13 (2), p.512

2015

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Transient Neonatal Zinc Deficiency Caused by a Heterozygous G87R Mutation in the Zinc Transporter ZnT-2 (SLC30A2) Gene in the Mother Highlighting the Importance of Zn 2+ for Normal Growth and Development

International journal of endocrinology, 2013, Vol.2013, p.1-8

2013

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Molecular analysis of the GNAS1 gene for the correct diagnosis of Albright hereditary osteodystrophy and pseudohypoparathyroidism

Pediatric research, 2003-05, Vol.53 (5), p.749-755

2003

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The natural history of the normal/mild elevated TSH serum levels in children and adolescents with Hashimoto's thyroiditis and isolated hyperthyrotropinaemia: a 3-year follow-up

Clinical endocrinology (Oxford), 2012-03, Vol.76 (3), p.394-398

2012

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A Family with Complete Resistance to Thyrotropin-Releasing Hormone

The New England journal of medicine, 2009-02, Vol.360 (7), p.731-734

2009

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Thyroid Function and Structure Are Affected in Childhood Obesity

The journal of clinical endocrinology and metabolism, 2008-12, Vol.93 (12), p.4749-4754

2008

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Frequency of genetic defects in combined pituitary hormone deficiency: a systematic review and analysis of a multicentre Italian cohort

Clinical endocrinology (Oxford), 2015-12, Vol.83 (6), p.849-860

2015

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Efficacy of long-term growth hormone therapy in short non-growth hormone-deficient children

Journal of pediatric endocrinology & metabolism : JPEM, 2017-02, Vol.30 (2), p.197

2017

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Age at Menarche and Menstrual Abnormalities in Adolescence: Does it Matter? The Evidence from a Large Survey among Italian Secondary Schoolgirls

Indian journal of pediatrics, 2019-02, Vol.86 (Suppl 1), p.34-41

2019

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Is retesting in growth hormone deficient children really useful?

Minerva endocrinologica, 2017-12, Vol.42 (4), p.325

2017

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Menstrual Cycle and Headache in Teenagers

Indian journal of pediatrics, 2019-02, Vol.86 (Suppl 1), p.25-33

2019

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Germline Prokineticin Receptor 2 (PROKR2) Variants Associated With Central Hypogonadism Cause Differental Modulation of Distinct Intracellular Pathways

The journal of clinical endocrinology and metabolism, 2014-03, Vol.99 (3), p.E458-E463

2014

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Emerging Effects of Early Environmental Factors over Genetic Background for Type 1 Diabetes Susceptibility: Evidence from a Nationwide Italian Twin Study

The journal of clinical endocrinology and metabolism, 2012-08, Vol.97 (8), p.E1483-E1491

2012

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New understandings of the genetic basis of isolated idiopathic central hypogonadism

Asian journal of andrology, 2012-01, Vol.14 (1), p.49-56

2012

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Clinical heterogeneity and diagnostic delay of autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome

Clinical immunology (Orlando, Fla.), 2011-04, Vol.139 (1), p.6-11

2011

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Characterizing Short Stature by Insulin-like Growth Factor Axis Status and Genetic Associations: Results From the Prospective, Cross-sectional, Epidemiogenetic EPIGROW Study

The journal of clinical endocrinology and metabolism, 2013-06, Vol.98 (6), p.E1122-E1130

2013

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Profound T-cell defects in Dubowitz syndrome

Pediatric allergy and immunology, 2014-08, Vol.25 (5), p.511-513

2014

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De novo deletion of chromosome 2q24.2 region in a mentally retarded boy with muscular hypotonia

European journal of medical genetics, 2011-05, Vol.54 (3), p.361-364

2011

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Impaired Growth during Childhood in Patients with Primary Ciliary Dyskinesia

Update on Age at Menarche in Italy: Toward the Leveling Off of the Secular Trend

Menstrual pattern and menstrual disorders among adolescents: an update of the Italian data

The levelling-off of the secular trend of age at menarche among Italian girls

Transient Neonatal Zinc Deficiency Caused by a Heterozygous G87R Mutation in the Zinc Transporter ZnT-2 (SLC30A2) Gene in the Mother Highlighting the Importance of Zn2+ for Normal Growth and Development

Onset of menstrual cycle and menses features among secondary school girls in Italy: A questionnaire study on 3,783 students

Early onset of puberty during COVID-19 pandemic lockdown: experience from two Pediatric Endocrinology Italian Centers

Primary Dysmenorrhea in Adolescents: Prevalence, Impact and Recent Knowledge

Transient Neonatal Zinc Deficiency Caused by a Heterozygous G87R Mutation in the Zinc Transporter ZnT-2 (SLC30A2) Gene in the Mother Highlighting the Importance of Zn 2+ for Normal Growth and Development

Molecular analysis of the GNAS1 gene for the correct diagnosis of Albright hereditary osteodystrophy and pseudohypoparathyroidism

The natural history of the normal/mild elevated TSH serum levels in children and adolescents with Hashimoto's thyroiditis and isolated hyperthyrotropinaemia: a 3-year follow-up

A Family with Complete Resistance to Thyrotropin-Releasing Hormone

Thyroid Function and Structure Are Affected in Childhood Obesity

Frequency of genetic defects in combined pituitary hormone deficiency: a systematic review and analysis of a multicentre Italian cohort

Efficacy of long-term growth hormone therapy in short non-growth hormone-deficient children

Age at Menarche and Menstrual Abnormalities in Adolescence: Does it Matter? The Evidence from a Large Survey among Italian Secondary Schoolgirls

Is retesting in growth hormone deficient children really useful?

Menstrual Cycle and Headache in Teenagers

Germline Prokineticin Receptor 2 (PROKR2) Variants Associated With Central Hypogonadism Cause Differental Modulation of Distinct Intracellular Pathways

Emerging Effects of Early Environmental Factors over Genetic Background for Type 1 Diabetes Susceptibility: Evidence from a Nationwide Italian Twin Study

New understandings of the genetic basis of isolated idiopathic central hypogonadism

Clinical heterogeneity and diagnostic delay of autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome

Characterizing Short Stature by Insulin-like Growth Factor Axis Status and Genetic Associations: Results From the Prospective, Cross-sectional, Epidemiogenetic EPIGROW Study

Profound T-cell defects in Dubowitz syndrome

De novo deletion of chromosome 2q24.2 region in a mentally retarded boy with muscular hypotonia

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