Beckwith–Wiedemann and IMAGe syndromes: two very different diseases caused by mutations on the same gene

por Milani, Donatella, Pezzani, Lidia, Tabano, Silvia, Miozzo, Monica
Publicado 2014

Fragile X syndrome: a review of clinical and molecular diagnoses

por Ciaccio, Claudia, Fontana, Laura, Milani, Donatella, Tabano, Silvia, Miozzo, Monica, Esposito, Susanna
Publicado 2017

A Rare Case of Urinary Bladder Hamartoma Clinically Mimicking an Urothelial Carcinoma: A Case Report and Review of the Literature

por Pescia, Carlo, Pini, Giuditta, Lopez, Gianluca, Malfatto, Matteo, Brescia, Gloria, Tabano, Silvia, Del Gobbo, Alessandro
Publicado 2023

The Classification of Myeloproliferative Neoplasms: Rationale, Historical Background and Future Perspectives with Focus on Unclassifiable Cases

por Pizzi, Marco, Croci, Giorgio Alberto, Ruggeri, Marco, Tabano, Silvia, Dei Tos, Angelo Paolo, Sabattini, Elena, Gianelli, Umberto
Publicado 2021

3D bioprinting of multi-layered segments of a vessel-like structure with ECM and novel derived bioink

por Potere, Federica, Belgio, Beatrice, Croci, Giorgio Alberto, Tabano, Silvia, Petrini, Paola, Dubini, Gabriele, Boschetti, Federica, Mantero, Sara
Publicado 2022

Analysis of BRCA1 and RAD51C Promoter Methylation in Italian Families at High-Risk of Breast and Ovarian Cancer

por Tabano, Silvia, Azzollini, Jacopo, Pesenti, Chiara, Lovati, Sara, Costanza, Jole, Fontana, Laura, Peissel, Bernard, Miozzo, Monica, Manoukian, Siranoush
Publicado 2020

Clinical and Molecular Diagnosis of Beckwith-Wiedemann Syndrome with Single- or Multi-Locus Imprinting Disturbance

por Fontana, Laura, Tabano, Silvia, Maitz, Silvia, Colapietro, Patrizia, Garzia, Emanuele, Gerli, Alberto Giovanni, Sirchia, Silvia Maria, Miozzo, Monica
Publicado 2021

MassARRAY-based simultaneous detection of hotspot somatic mutations and recurrent fusion genes in papillary thyroid carcinoma: the PTC-MA assay

por Pesenti, Chiara, Muzza, Marina, Colombo, Carla, Proverbio, Maria Carla, Farè, Claudia, Ferrero, Stefano, Miozzo, Monica, Fugazzola, Laura, Tabano, Silvia
Publicado 2017

Genetic Polymorphisms and Sepsis in Premature Neonates

por Esposito, Susanna, Zampiero, Alberto, Pugni, Lorenza, Tabano, Silvia, Pelucchi, Claudio, Ghirardi, Beatrice, Terranova, Leonardo, Miozzo, Monica, Mosca, Fabio, Principi, Nicola
Publicado 2014

972 Impact of Genetic Polymorphisms on the Risk of Sepsis in Premature Neonates

por Esposito, Susanna, Zampiero, Alberto, Pugni, Lorenza, Tabano, Silvia, Pelucchi, Claudio, Ghirardi, Beatrice, Terranova, Leonardo, Miozzo, Monica, Mosca, Fabio, Principi, Nicola
Publicado 2014

New case of trichorinophalangeal syndrome-like phenotype with a de novo t(2;8)(p16.1;q23.3) translocation which does not disrupt the TRPS1 gene

por Crippa, Milena, Bestetti, Ilaria, Perotti, Mario, Castronovo, Chiara, Tabano, Silvia, Picinelli, Chiara, Grassi, Guido, Larizza, Lidia, Pincelli, Angela Ida, Finelli, Palma
Publicado 2014

Profound alterations of the chromatin architecture at chromosome 11p15.5 in cells from Beckwith-Wiedemann and Silver-Russell syndromes patients

por Rovina, Davide, La Vecchia, Marta, Cortesi, Alice, Fontana, Laura, Pesant, Matthieu, Maitz, Silvia, Tabano, Silvia, Bodega, Beatrice, Miozzo, Monica, Sirchia, Silvia M.
Publicado 2020

MV1035 Overcomes Temozolomide Resistance in Patient-Derived Glioblastoma Stem Cell Lines

por Malacrida, Alessio, Di Domizio, Alessandro, Bentivegna, Angela, Cislaghi, Giacomo, Messuti, Eleonora, Tabano, Silvia Maria, Giussani, Carlo, Zuliani, Valentina, Rivara, Mirko, Nicolini, Gabriella
Publicado 2022

Misbehaviour of XIST RNA in Breast Cancer Cells

por Sirchia, Silvia M., Tabano, Silvia, Monti, Laura, Recalcati, Maria P., Gariboldi, Manuela, Grati, Francesca R., Porta, Giovanni, Finelli, Palma, Radice, Paolo, Miozzo, Monica
Publicado 2009

Preferential X Chromosome Inactivation as a Mechanism to Explain Female Preponderance in Myasthenia Gravis

por Nicolì, Vanessa, Tabano, Silvia Maria, Colapietro, Patrizia, Maestri, Michelangelo, Ricciardi, Roberta, Stoccoro, Andrea, Fontana, Laura, Guida, Melania, Miozzo, Monica, Coppedè, Fabio, Migliore, Lucia
Publicado 2022

Beckwith–Wiedemann syndrome prenatal diagnosis by methylation analysis in chorionic villi

por Paganini, Leda, Carlessi, Nicole, Fontana, Laura, Silipigni, Rosamaria, Motta, Silvia, Fiori, Stefano, Guerneri, Silvana, Lalatta, Faustina, Cereda, Anna, Sirchia, Silvia, Miozzo, Monica, Tabano, Silvia
Publicado 2015

Preferential expression of mutant ABCD1 allele is common in adrenoleukodystrophy female carriers but unrelated to clinical symptoms

por Salsano, Ettore, Tabano, Silvia, Sirchia, Silvia M, Colapietro, Patrizia, Castellotti, Barbara, Gellera, Cinzia, Rimoldi, Marco, Pensato, Viviana, Mariotti, Caterina, Pareyson, Davide, Miozzo, Monica, Uziel, Graziella
Publicado 2012

Revertant mosaicism for family mutations is not observed in BRCA1/2 phenocopies

por Azzollini, Jacopo, Pesenti, Chiara, Ferrari, Luca, Fontana, Laura, Calvello, Mariarosaria, Peissel, Bernard, Portera, Giorgio, Tabano, Silvia, Carcangiu, Maria Luisa, Riva, Paola, Miozzo, Monica, Manoukian, Siranoush
Publicado 2017

Prognostic value of preoperative von Willebrand factor plasma levels in patients with Glioblastoma

por Marfia, Giovanni, Navone, Stefania Elena, Fanizzi, Claudia, Tabano, Silvia, Pesenti, Chiara, Abdel Hadi, Loubna, Franzini, Andrea, Caroli, Manuela, Miozzo, Monica, Riboni, Laura, Rampini, Paolo, Campanella, Rolando
Publicado 2016

Delineating the Cytogenomic and Epigenomic Landscapes of Glioma Stem Cell Lines

por Baronchelli, Simona, Bentivegna, Angela, Redaelli, Serena, Riva, Gabriele, Butta, Valentina, Paoletta, Laura, Isimbaldi, Giuseppe, Miozzo, Monica, Tabano, Silvia, Daga, Antonio, Marubbi, Daniela, Cattaneo, Monica, Biunno, Ida, Dalprà, Leda
Publicado 2013