Publications by authors named "Laura Filonzi"

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The Changing Epidemiology of Sudden Infant Death Syndrome: A 15-Year Overview Comparing Italian and European Data.
Matteo Manfredini, Serafina Perrone, Alessia Ardenghi, Anna Maria Lavezzi, Virginia Beretta, Laura Filonzi

Health Sci Rep· March 2025

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Hypoxic ischemic brain injury: animal models reveal new mechanisms of melatonin-mediated neuroprotection.
Serafina Perrone, Silvia Carloni, Valentina Giovanna Dell'Orto, Laura Filonzi, Virginia Beretta

Rev Neurosci· April 2024

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Molecular Barcoding: A Tool to Guarantee Correct Seafood Labelling and Quality and Preserve the Conservation of Endangered Species.
Laura Filonzi, Alessia Ardenghi, Pietro Maria Rontani, Andrea Voccia, Claudio Ferrari

Foods· June 2023

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Vascular Endothelial Growth Factor as Molecular Target for Bronchopulmonary Dysplasia Prevention in Very Low Birth Weight Infants.
Serafina Perrone, Sara Manti, Luca Buttarelli, Chiara Petrolini, Giovanni Boscarino, Laura Filonzi

Int J Mol Sci· February 2023

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Molecular Polymorphisms of Vascular Endothelial Growth Factor Gene and Bronchopulmonary Dysplasia in Very Low Birth Weight Infants.
Laura Filonzi, Serafina Perrone, Maria Luisa Tataranno, Cinzia Magnani, Harold Dadomo

Dis Markers· September 2022

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Efficiency of DNA Mini-Barcoding to Assess Mislabeling in Commercial Fish Products in Italy: An Overview of the Last Decade.
Laura Filonzi, Marina Vaghi, Alessia Ardenghi, Pietro Maria Rontani, Andrea Voccia

Foods· June 2021

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Detoxification genes polymorphisms in SIDS exposed to tobacco smoke.
Laura Filonzi, Cinzia Magnani, Anna Maria Lavezzi, Marina Vaghi, Luana Nosetti

Gene· March 2018

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Null alleles of microsatellites for Manila clam Ruditapes philippinarum.
Stefania Chiesa, Livia Lucentini, Rosa Freitas, Francesco Nonnis Marzano, Claudio Ferrari, Laura Filonzi

Anim Genet· February 2016

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Molecular barcoding of an atypical cyprinid population assessed by cytochrome B gene sequencing.
Stefania Chiesa, Laura Filonzi, Marina Vaghi, Riccardo Papa, Francesco Nonnis Marzano

Zoolog Sci· May 2013

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Serotonin transporter role in identifying similarities between SIDS and idiopathic ALTE.
Laura Filonzi, Cinzia Magnani, Luana Nosetti, Luigi Nespoli, Camilla Borghi

Pediatrics· July 2012

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Confirmed association between monoamine oxidase A molecular polymorphisms and Sudden Infant Death Syndrome.
Laura Filonzi, Cinzia Magnani, Francesco Nonnis Marzano

Neurogenetics· February 2011

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Evidence that polymorphic deletion of the glutathione S-transferase gene, GSTM1, is associated with esophageal atresia.
Laura Filonzi, Cinzia Magnani, Gian Luigi de' Angelis, Sara Dallaglio, Francesco Nonnis Marzano

Birth Defects Res A Clin Mol Teratol· September 2010

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Association of dopamine transporter and monoamine oxidase molecular polymorphisms with sudden infant death syndrome and stillbirth: new insights into the serotonin hypothesis.
Laura Filonzi, Cinzia Magnani, Anna Maria Lavezzi, Guido Rindi, Stefano Parmigiani

Neurogenetics· February 2009

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Genes regulating the serotonin metabolic pathway in the brain stem and their role in the etiopathogenesis of the sudden infant death syndrome.
Francesco Nonnis Marzano, Milena Maldini, Laura Filonzi, Anna Maria Lavezzi, Stefano Parmigiani

Genomics· June 2008

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