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American Journal of Medical Genetics. Part A|March 28, 2017
ZC4H2 deletions can cause severe phenotype in female carriersCristina Zanzottera, Donatella Milani, Enrico Alfei, et al.Cancers|June 10, 2023
The Role of Adhesion Molecules and Extracellular Vesicles in an In Vitro Model of the Blood-Brain Barrier for Metastatic DiseaseChiara Vasco, Ambra Rizzo, Chiara Cordiglieri, et al.Journal of Experimental & Clinical Cancer Research : CR|June 8, 2017
In vitro antineoplastic effects of brivaracetam and lacosamide on human glioma cellsAmbra Rizzo, Sara Donzelli, Vita Girgenti, et al.Journal of Neuro-Oncology|September 6, 2013
Circulating T regulatory cells migration and phenotype in glioblastoma patients: an in vitro studyChiara Vasco, Alessandra Canazza, Ambra Rizzo, et al.Nutrition and Cancer|September 21, 2020
MR-Spectroscopy and Survival in Mice with High Grade Glioma Undergoing Unrestricted Ketogenic DietEmilio Ciusani, Chiara Vasco, Ambra Rizzo, et al.Stem Cell Research|January 12, 2021
Generation of two human iPSC lines, FINCBi002-A and FINCBi003-A, carrying heteroplasmic macrodeletion of mitochondrial DNA causing Pearson's syndromeCamille Peron, Roberta Mauceri, Angelo Iannielli, et al.Journal of Autism and Developmental Disorders|January 4, 2021
CGH Findings in Children with Complex and Essential Autistic Spectrum DisorderSilvia Annunziata, Sara Bulgheroni, Stefano D'Arrigo, et al.Stem Cell Research|August 11, 2020
Generation of a human iPSC line, FINCBi001-A, carrying a homoplasmic m.G3460A mutation in MT-ND1 associated with Leber's Hereditary optic Neuropathy (LHON)Camille Peron, Roberta Mauceri, Tommaso Cabassi, et al.Molecular Cancer|December 17, 2013
Frequency of NFKBIA deletions is low in glioblastomas and skewed in glioblastoma neurospheresMonica Patanè, Paola Porrati, Elisa Bottega, et al.European Journal of Medical Genetics|February 14, 2013
MEF2C deletions and mutations versus duplications: a clinical comparisonFrancesca Novara, Ambra Rizzo, Gloria Bedini, et al.Pageof 2