Publications by authors named "Cinzia Magnani"

34 Publications

Lowry-Wood syndrome: further evidence of association with RNU4ATAC, and correlation between genotype and phenotype.

Hum Genet 2018 Dec 27;137(11-12):905-909. Epub 2018 Oct 27.

Divisions of Medical Genetics, Department of Pediatrics, CHU Sainte-Justine, Université de Montréal, Montreal, QC, Canada.

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December 2018

Detoxification genes polymorphisms in SIDS exposed to tobacco smoke.

Gene 2018 Mar 9;648:1-4. Epub 2018 Jan 9.

Department of Chemistry, Life Sciences and Environmental Sustainability, University of Parma, Parco Area delle Scienze 11/A, Parma, Italy. Electronic address:

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March 2018

Universal newborn hearing screening: the experience of the University Hospital of Parma.

Acta Biomed 2015 Dec 15;86(3):273-7. Epub 2015 Dec 15.

Neonatology and Neonatal Intensive Care Unit, Maternal and Child Department, University of Parma - Parma, Italy.

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December 2015

Neonatal forearm compartment syndrome: look for cerebral stroke.

J Pediatr 2014 Feb 16;164(2):427.e1. Epub 2013 Nov 16.

Child Neuropsychiatry Unit, Neuroscience Department, Parma University, Parma, Italy.

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February 2014

Unilateral ectopic parotid gland in CHARGE syndrome.

Pediatr Radiol 2013 Jan 5;43(2):247-51. Epub 2012 Dec 5.

Department of Neuroradiology, Azienda Ospedaliero-Universitaria di Parma, Via Gramsci 14, 43126 Parma, Italy.

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January 2013

Serotonin transporter role in identifying similarities between SIDS and idiopathic ALTE.

Pediatrics 2012 Jul 18;130(1):e138-44. Epub 2012 Jun 18.

Department of Evolutionary and Functional Biology, University of Parma, Parma, Italy.

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July 2012

Mandibular distraction in neonates: indications, technique, results.

Ital J Pediatr 2012 Feb 2;38. Epub 2012 Feb 2.

Maxillo-Facial Surgery Division, Head and Neck Department, University and Hospital of Parma, Parma, Italy.

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February 2012

SMC1A codon 496 mutations affect the cellular response to genotoxic treatments.

Am J Med Genet A 2012 Jan 2;158A(1):224-8. Epub 2011 Dec 2.

Istituto di Ricerca Genetica e Biomedica, Consiglio Nazionale delle Ricerche, Pisa, Italy.

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January 2012

Apparent life threatening event and gastric antral ulcer in a full-term infant: any possible relationship?

Acta Biomed 2010 Sep;81(2):144-6

Department of Gynecology, Obstetrics and Neonatological Sciences, University Hospital, Parma, Italy.

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September 2010

Craniosynostosis: prenatal diagnosis by means of ultrasound and SSSE-MRI. Family series with report of neurodevelopmental outcome and review of the literature.

Arch Gynecol Obstet 2011 Apr 2;283(4):909-16. Epub 2010 Sep 2.

Division of Obstetrics and Gynecology, Prenatal Diagnostic Center, Guastalla Civil Hospital, AUSL Reggio Emilia, Via Donatori Sangue, 1, 42016 Guastalla (Reggio Emilia), Italy.

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April 2011

Evidence that polymorphic deletion of the glutathione S-transferase gene, GSTM1, is associated with esophageal atresia.

Birth Defects Res A Clin Mol Teratol 2010 Sep;88(9):743-7

Department of Evolutionary and Functional Biology, University of Parma, Parma, Italy.

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September 2010

Congenital cervical teratoma: a case report.

J Oral Maxillofac Surg 2010 Mar 18;68(3):667-70. Epub 2009 Nov 18.

Head and Neck Department, Maxillo-Facial Surgery Division, University and Hospital of Parma, Parma, Italy.

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March 2010