Publications by authors named "Roberta Oneda"

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Obstructive sleep apnea syndrome (OSAS) in children with Class III malocclusion: involvement of the PHOX2B gene.
Anna Maria Lavezzi, Valentina Casale, Roberta Oneda, Silvia Gioventù, Luigi Matturri

Sleep Breath· December 2013

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Sudden death of an infant with cardiac, nervous system and genetic involvement--a case report.
Donatella Mecchia, Valentina Casale, Roberta Oneda, Luigi Matturri, Anna Maria Lavezzi

Diagn Pathol· September 2013

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Investigation of 5-HTT expression using quantitative real-time PCR in the human brain in SIDS Italian cases.
Valentina Casale, Roberta Oneda, Luigi Matturri, Anna Maria Lavezzi

Exp Mol Pathol· February 2013

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Developmental alterations of the respiratory human retrotrapezoid nucleus in sudden unexplained fetal and infant death.
Anna M Lavezzi, Debra E Weese-Mayer, Margaret Y Yu, Lawrence J Jennings, Melissa F Corna, Roberta Oneda

Auton Neurosci· September 2012

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Optimisation of postmortem tissue preservation and alternative protocol for serotonin transporter gene polymorphisms amplification in SIDS and SIUD cases.
Valentina Casale, Roberta Oneda, Anna Maria Lavezzi, Luigi Matturri

Exp Mol Pathol· February 2010

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Sudden infant death syndrome and sudden intrauterine unexplained death: correlation between hypoplasia of raphé nuclei and serotonin transporter gene promoter polymorphism.
Anna M Lavezzi, Valentina Casale, Roberta Oneda, Debra E Weese-Mayer, Luigi Matturri

Pediatr Res· July 2009

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A UV-sensitive syndrome patient with a specific CSA mutation reveals separable roles for CSA in response to UV and oxidative DNA damage.
Tiziana Nardo, Roberta Oneda, Graciela Spivak, Bruno Vaz, Laurent Mortier

Proc Natl Acad Sci U S A· April 2009

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