Publications by authors named "Simona Madeo"

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The burden of extra uterine growth restriction on postnatal growth in very low birth weight preterm newborns.
Laura Lucaccioni, Elisa Pietrella, Giovanni Malmusi, Giulia Cinelli, Francesco Candia, Simona Filomena Madeo

BMC Pediatr· November 2025

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Mometasone Furoate-Induced Iatrogenic Cushing's Syndrome and Secondary Adrenal Insufficiency: A Case Report.
Anna Insalaco, Sara Vandelli, Simona F Madeo, Patrizia Bruzzi, Viola Trevisani

Case Rep Pediatr· June 2025

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Lack of correlation between asprosin serum levels and hyperphagic behavior in subjects with prader-Willi Syndrome.
Maria Felicia Faienza, Mariangela Chiarito, Alessia Aureli, Raffaele Buganza, Domenico Corica, Simona Madeo

J Endocrinol Invest· April 2025

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Endocrine features of Prader-Willi syndrome: a narrative review focusing on genotype-phenotype correlation.
Simona F Madeo, Luca Zagaroli, Sara Vandelli, Valeria Calcaterra, Antonino Crinò

Front Endocrinol (Lausanne)· May 2024

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The Approach to a Child with Dysmorphic Features: What the Pediatrician Should Know.
Silvia Ciancia, Simona Filomena Madeo, Olga Calabrese, Lorenzo Iughetti

Children (Basel)· May 2024

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Deep phenotyping of the neuroimaging and skeletal features in KBG syndrome: a study of 53 patients and review of the literature.
Francesca Peluso, Stefano G Caraffi, Gianluca Contrò, Lara Valeri, Manuela Napoli, Simona F Madeo

J Med Genet· November 2023

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The impact of BMI on long-term anthropometric and metabolic outcomes in girls with idiopathic central precocious puberty treated with GnRHas.
Patrizia Bruzzi, Lara Valeri, Marcello Sandoni, Simona Filomena Madeo, Barbara Predieri

Front Endocrinol (Lausanne)· October 2022

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Copy Number Variation Analysis Increases the Number of Candidate Loci Associated with Pediatric Obesity.
Simona Filomena Madeo, Ilaria Stanghellini, Barbara Predieri, Silvia Ciancia, Francesco Leo

Horm Res Paediatr· March 2022

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Growth hormone deficiency in a child with benign hereditary chorea caused by a mutation of the TITF1/NKX2-1 gene.
Viola Trevisani, Barbara Predieri, Simona Filomena Madeo, Carlo Fusco, Livia Garavelli

J Pediatr Endocrinol Metab· March 2022

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Recurrent NF1 gene variants and their genotype/phenotype correlations in patients with Neurofibromatosis type I.
Matteo Riva, Davide Martorana, Vera Uliana, Edoardo Caleffi, Elena Boschi, Simona Madeo

Genes Chromosomes Cancer· January 2022

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Longitudinal evaluation of endothelial markers in children and adolescents with familial hypercholesterolemia.
Patrizia Bruzzi, Barbara Predieri, Simona Madeo, Francesca Lami, Lorenzo Iughetti

Acta Biomed· November 2021

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EEG Patterns in Patients with Prader-Willi Syndrome.
Maurizio Elia, Irene Rutigliano, Michele Sacco, Simona F Madeo, Malgorzata Wasniewska

Brain Sci· August 2021

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Homozygous n.64C>T mutation in mitochondrial RNA-processing endoribonuclease gene causes cartilage hair hypoplasia syndrome in two siblings.
Licia Lugli, Silvia Ciancia, Emma Bertucci, Laura Lucaccioni, Olga Calabrese, Simona Madeo

Eur J Med Genet· February 2021

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Glycemic Control Improvement in Italian Children and Adolescents With Type 1 Diabetes Followed Through Telemedicine During Lockdown Due to the COVID-19 Pandemic.
Barbara Predieri, Francesco Leo, Francesco Candia, Laura Lucaccioni, Simona F Madeo

Front Endocrinol (Lausanne)· January 2021

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Health-related quality of life and metabolic control in immigrant and Italian children and adolescents with type 1 diabetes and in their parents.
Barbara Predieri, Patrizia Bruzzi, Elena Bigi, Alessandra Boncompagni, Federica Bocchi, Simona F Madeo

Pediatr Diabetes· September 2020

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COVID-19 and Type 1 Diabetes: Concerns and Challenges.
Lorenzo Iughetti, Viola Trevisani, Umberto Cattini, Patrizia Bruzzi, Laura Lucaccioni, Simona Madeo

Acta Biomed· September 2020

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Uniparental disomy and pretreatment IGF-1 may predict elevated IGF-1 levels in Prader-Willi patients on GH treatment.
Viviana Valeria Palmieri, Antonella Lonero, Sarah Bocchini, Gilda Cassano, Alessio Convertino, Simona Filomena Madeo

Growth Horm IGF Res· May 2020

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Endocrine Disrupting Chemicals and Type 1 Diabetes.
Barbara Predieri, Patrizia Bruzzi, Elena Bigi, Silvia Ciancia, Simona F Madeo

Int J Mol Sci· April 2020

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Anthropometric characteristics of newborns with Prader-Willi syndrome.
Alessandro Salvatoni, Alex Moretti, Graziano Grugni, Massimo Agosti, Sara Azzolini, Simona F Madeo

Am J Med Genet A· October 2019

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Isolated hypoaldosteronism as first sign of X-linked adrenal hypoplasia congenita caused by a novel mutation in NR0B1/DAX-1 gene: a case report.
Lorenzo Iughetti, Laura Lucaccioni, Patrizia Bruzzi, Silvia Ciancia, Elena Bigi, Simona Filomena Madeo

BMC Med Genet· June 2019

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Central Precocious Puberty and Response to GnRHa Therapy in Children with Cerebral Palsy and Moderate to Severe Motor Impairment: Data from a Longitudinal, Case-Control, Multicentre, Italian Study.
Patrizia Bruzzi, Maria Francesca Messina, Alessandra Bartoli, Barbara Predieri, Laura Lucaccioni, Simona Filomena Madeo

Int J Endocrinol· July 2017

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Ten-year longitudinal study of thyroid function in children with Down's syndrome.
Lorenzo Iughetti, Barbara Predieri, Patrizia Bruzzi, Flavia Predieri, Giulia Vellani, Simona Filomena Madeo

Horm Res Paediatr· May 2015

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Short stature homeoboxcontaining gene and idiopathic short stature.
Lorenzo Iughetti, Petronilla Appio, Lucia Capone, Simona Madeo, Barbara Predieri

Expert Rev Endocrinol Metab· May 2009

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Low-density lipoprotein oxidizability in children with chronic renal failure.
Lorenzo Iughetti, Cristina Perugini, Barbara Predieri, Simona Madeo, Giorgio Bellomo

Pediatr Int· August 2008

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