Publications by authors named "Carlo Corbetta"

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A new approach to study stochastic epigenetic mutations in sperm methylome of Vietnam war veterans directly exposed to Agent Orange.
Luigi Corsaro, Davide Sacco, Carlo Corbetta, Davide Gentilini, Alice Faversani

Environ Epigenet· November 2024

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Fifteen Years of Iodine Prophylaxis in Italy: Results of a Nationwide Surveillance (Period 2015-2019).
Simona De Angelis, Emanuela Medda, Daniela Rotondi, Maria Masocco, Valentina Minardi, Carlo Corbetta

J Clin Endocrinol Metab· January 2024

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Newborn Screening for Congenital Hypothyroidism: the Benefit of Using Differential TSH Cutoffs in a 2-Screen Program.
Silvana Caiulo, Carlo Corbetta, Marianna Di Frenna, Emanuela Medda, Simona De Angelis

J Clin Endocrinol Metab· January 2021

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Phenotypic spectrum of short-chain enoyl-Coa hydratase-1 (ECHS1) deficiency.
Silvia Masnada, Cecilia Parazzini, Paolo Bini, Mario Barbarini, Luisella Alberti, Carlo Corbetta

Eur J Paediatr Neurol· September 2020

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The Italian External Quality Assessment Program for Cystic Fibrosis Sweat Chloride Test: Does Active Participation Improve the Quality?
Marco Salvatore, Annalisa Amato, Giovanna Floridia, Federica Censi, Gianluca Ferrari, Carlo Corbetta

Int J Environ Res Public Health· May 2020

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A New Targeted CFTR Mutation Panel Based on Next-Generation Sequencing Technology.
Marco Lucarelli, Luigi Porcaro, Alice Biffignandi, Lucy Costantino, Valentina Giannone, Carlo Corbetta

J Mol Diagn· September 2017

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The Italian pilot external quality assessment program for cystic fibrosis sweat test.
Marco Salvatore, Giovanna Floridia, Annalisa Amato, Federica Censi, Claudio Carta, Carlo Corbetta

Clin Biochem· May 2016

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A column-switching HPLC-MS/MS method for mucopolysaccharidosis type I analysis in a multiplex assay for the simultaneous newborn screening of six lysosomal storage disorders.
Antonina Gucciardi, Elisa Legnini, Iole Maria Di Gangi, Carlo Corbetta, Rosella Tomanin

Biomed Chromatogr· August 2014

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Evolution of thyroid function in preterm infants detected by screening for congenital hypothyroidism.
Maria Cristina Vigone, Silvana Caiulo, Marianna Di Frenna, Stefano Ghirardello, Carlo Corbetta

J Pediatr· June 2014

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Congenital hypothyroidism with eutopic thyroid gland: analysis of clinical and biochemical features at diagnosis and after re-evaluation.
Sarah Rabbiosi, Maria Cristina Vigone, Francesca Cortinovis, Ilaria Zamproni, Laura Fugazzola, Carlo Corbetta

J Clin Endocrinol Metab· April 2013

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Congenital hypothyroidism due to defects of thyroid development and mild increase of TSH at screening: data from the Italian National Registry of infants with congenital hypothyroidism.
Antonella Olivieri, Carlo Corbetta, Giovanna Weber, Maria Cristina Vigone, Cristina Fazzini

J Clin Endocrinol Metab· April 2013

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Cystic fibrosis newborn screening: distribution of blood immunoreactive trypsinogen concentrations in hypertrypsinemic neonates.
Valentina Paracchini, Manuela Seia, Sara Raimondi, Lucy Costantino, Patrizia Capasso, Carlo Corbetta

JIMD Rep· February 2013

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Common criteria among States for storage and use of dried blood spot specimens after newborn screening.
Carlo Petrini, Antonella Olivieri, Carlo Corbetta, Roberto Cerone, Giuliano D'Agnolo

Ann Ist Super Sanita· November 2012

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Metabolic screening for the newborn.
Rossella Parini, Carlo Corbetta

J Matern Fetal Neonatal Med· October 2011

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Storage and use of residual newborn screening dot blood samples in Italy.
Carlo Petrini, Antonella Olivieri, Carlo Corbetta, Roberto Cerone, Giuliano D'Agnolo

Ital J Pediatr· May 2011

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Newborn of mothers affected by autoimmune thyroiditis: the importance of thyroid function monitoring in the first months of life.
Rosanna Rovelli, Maria Cristina Vigone, Chiara Giovanettoni, Arianna Passoni, Ludovica Maina, Carlo Corbetta

Ital J Pediatr· March 2010

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Pp65 antigenemia, plasma real-time PCR and DBS test in symptomatic and asymptomatic cytomegalovirus congenitally infected newborns.
Sandro Binda, Antonella Mammoliti, Valeria Primache, Patrizia Didò, Carlo Corbetta

BMC Infect Dis· February 2010

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A 7-year experience with low blood TSH cutoff levels for neonatal screening reveals an unsuspected frequency of congenital hypothyroidism (CH).
Carlo Corbetta, Giovanna Weber, Francesca Cortinovis, Davide Calebiro, Arianna Passoni

Clin Endocrinol (Oxf)· November 2009

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European best practice guidelines for cystic fibrosis neonatal screening.
Carlo Castellani, Kevin W Southern, Keith Brownlee, Jeannette Dankert Roelse, Alistair Duff, Carlo Corbetta

J Cyst Fibros· May 2009

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Borderline sweat test: Utility and limits of genetic analysis for the diagnosis of cystic fibrosis.
Manuela Seia, Lucy Costantino, Valentina Paracchini, Luigi Porcaro, Patrizia Capasso, Carlo Corbetta

Clin Biochem· May 2009

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Glucose metabolism and diet-based prevention of liver dysfunction in MPV17 mutant patients.
Rossella Parini, Francesca Furlan, Luigi Notarangelo, Antonella Spinazzola, Graziella Uziel, Carlo Corbetta

J Hepatol· January 2009

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Neonatal thyroid function in Seveso 25 years after maternal exposure to dioxin.
Andrea Baccarelli, Sara M Giacomini, Carlo Corbetta, Maria Teresa Landi, Matteo Bonzini

PLoS Med· July 2008

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Identification of the 5T-12TG allele of the cystic fibrosis transmembrane conductance regulator gene in hypertrypsinaemic newborns.
Rita Padoan, Carlo Corbetta, Alessandra Bassotti, Manuela Seia

Acta Paediatr· July 2006

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A wider role for congenital cytomegalovirus infection in sensorineural hearing loss.
Maria Barbi, Sandro Binda, Simona Caroppo, Umberto Ambrosetti, Carlo Corbetta

Pediatr Infect Dis J· January 2003

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Negative sweat test in hypertrypsinaemic infants with cystic fibrosis carrying rare CFTR mutations.
Rita Padoan, Alessandra Bassotti, Manuela Seia, Carlo Corbetta

Eur J Pediatr· April 2002

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