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European Journal of Pediatrics|January 27, 2017
Developmental trends of communicative skills in children with chromosome 14 aberrationsLaura Zampini, Paola Zanchi, Berardo Rinaldi, et al.
Clinical, Cosmetic and Investigational Dentistry|January 1, 2016
Scanning electron microscopy analysis of the growth of dental plaque on the surfaces of removable orthodontic aligners after the use of different cleaning methodsLuca Levrini, Francesca Novara, Silvia Margherini, et al.
Case Reports in Obstetrics and Gynecology|September 12, 2014
A Therapeutic Challenge: Liddle's Syndrome Managed with Amiloride during PregnancyAmelia Caretto, Liviana Primerano, Francesca Novara, et al.
Epilepsy & Behavior : E&B|November 20, 2012
22q11.2 Microduplication syndrome and epilepsy with continuous spikes and waves during sleep (CSWS). A case report and review of the literatureGiulia Valvo, Francesca Novara, Paola Brovedani, et al.
European Journal of Medical Genetics|December 3, 2014
Heterozygous deletion of CHL1 gene: detailed array-CGH and clinical characterization of a new case and review of the literatureElisa Tassano, Roberta Biancheri, Laura Denegri, et al.
Leukemia & Lymphoma|September 2, 2011
Three cases of primary cutaneous lymphoblastic lymphoma: microarray-based comparative genomic hybridization and gene expression profiling studies with review of literaturePamela Vezzoli, Francesca Novara, Daniele Fanoni, et al.
Molecular Cytogenetics|January 30, 2014
MECP2 duplication phenotype in symptomatic females: report of three further casesFrancesca Novara, Alessandro Simonati, Federico Sicca, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|March 28, 2013
Neonatal suppression-burst without epileptic seizures: expanding the electroclinical phenotype of STXBP1-related, early-onset encephalopathyMassimo Mastrangelo, Angela Peron, Luigina Spaccini, et al.
European Journal of Human Genetics : EJHG|November 1, 2006
Cortical dysplasia of the left temporal lobe might explain severe expressive-language delay in patients with duplication of the Williams-Beuren locusClaudia Torniero, Bernardo dalla Bernardina, Francesca Novara, et al.
European Journal of Human Genetics : EJHG|March 14, 2008
Dysmorphic features, simplified gyral pattern and 7q11.23 duplication reciprocal to the Williams-Beuren deletionClaudia Torniero, Bernardo Dalla Bernardina, Francesca Novara, et al.
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