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European Journal of Medical Genetics|September 19, 2016
Human teratogens and genetic phenocopies. Understanding pathogenesis through human genes mutationMatteo Cassina, Giulia A Cagnoli, Daniela Zuccarello, et al.
Prenatal Diagnosis|July 19, 2002
Prenatal ultrasonographic detection of gastrointestinal obstruction: results from 18 European congenital anomaly registriesMartin C H Haeusler, Andrea Berghold, Claude Stoll, et al.
Reproductive Toxicology (Elmsford, N.Y.)|July 16, 2008
The role of toxicology to characterize biomarkers for agrochemicals with potential endocrine activitiesAlberto Mantovani, Francesca Maranghi, Cinzia La Rocca, et al.
Expert Opinion on Drug Safety|July 29, 2010
Migraine therapy during pregnancy and lactationMatteo Cassina, Elena Di Gianantonio, Irene Toldo, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology|December 13, 2017
Prenatal detection of trisomy 8 mosaicism: Pregnancy outcome and follow up of a series of 17 consecutive casesMatteo Cassina, Annapaola Calò, Leonardo Salviati, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology|March 11, 2006
Pregnancy outcome after genetic counselling for prenatal diagnosis of unexpected chromosomal anomalyMaurizio Clementi, Elena Di Gianantonio, Rossella Ponchia, et al.
Autoimmunity Reviews|March 24, 2010
Bisphosphonates in patients with autoimmune rheumatic diseases: Can they be used in women of childbearing age?Inès Losada, Leonardo Sartori, Elena Di Gianantonio, et al.
Drug Safety|April 3, 2009
First-trimester itraconazole exposure and pregnancy outcome: a prospective cohort study of women contacting teratology information services in ItalyMarco De Santis, Elena Di Gianantonio, Elena Cesari, et al.
The Journal of Clinical Endocrinology and Metabolism|July 30, 2010
Treatment of hyperthyroidism in pregnancy and birth defectsMaurizio Clementi, Elena Di Gianantonio, Matteo Cassina, et al.
European Journal of Human Genetics : EJHG|December 15, 2016
A synonymous splicing mutation in the SF3B4 gene segregates in a family with highly variable Nager syndromeMatteo Cassina, Cristina Cerqua, Silvia Rossi, et al.
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