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Pediatric Radiology|December 6, 2012
Unilateral ectopic parotid gland in CHARGE syndromeFrancesca Ormitti, Elisa Ventura, Andrea Bacciu, et al.
Acta Bio-Medica : Atenei Parmensis|February 11, 2011
Apparent life threatening event and gastric antral ulcer in a full-term infant: any possible relationship?Pier Luigi Bacchini, Enzo Romanini, Cinzia Magnani, et al.
Acta Bio-Medica : Atenei Parmensis|October 30, 2013
Are there any strategies to improve neonatal outcomes associated with epidural analgesia in labor?Marta Armani, Carla Gaggiano, Sara Dallaglio, et al.
Italian Journal of Pediatrics|February 4, 2012
Mandibular distraction in neonates: indications, technique, resultsEnrico Sesenna, Alice S Magri, Cinzia Magnani, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|August 27, 2010
Evidence that polymorphic deletion of the glutathione S-transferase gene, GSTM1, is associated with esophageal atresiaLaura Filonzi, Cinzia Magnani, Gian Luigi de' Angelis, et al.
Gene|January 14, 2018
Detoxification genes polymorphisms in SIDS exposed to tobacco smokeLaura Filonzi, Cinzia Magnani, Anna Maria Lavezzi, et al.
Archives of Gynecology and Obstetrics|September 3, 2010
Craniosynostosis: prenatal diagnosis by means of ultrasound and SSSE-MRI. Family series with report of neurodevelopmental outcome and review of the literatureGabriele Tonni, Marco Panteghini, Andrea Rossi, et al.
American Journal of Medical Genetics. Part A|December 6, 2011
SMC1A codon 496 mutations affect the cellular response to genotoxic treatmentsLinda Mannini, Stefania Menga, Alessandra Tonelli, et al.
Pediatrics|June 20, 2012
Serotonin transporter role in identifying similarities between SIDS and idiopathic ALTELaura Filonzi, Cinzia Magnani, Luana Nosetti, et al.
Human Genetics|October 29, 2018
Lowry-Wood syndrome: further evidence of association with RNU4ATAC, and correlation between genotype and phenotypeIvan Shelihan, Sophie Ehresmann, Cinzia Magnani, et al.
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