Finding the way to Wilms tumor by comparing the primary and relapse tumor samples

por Spreafico, Filippo, Ciceri, Sara, Perotti, Daniela
Publicado 2022

The IGF signalling pathway in Wilms tumours - A report from the ENCCA Renal Tumours Biology-driven drug development workshop

por Maschietto, Mariana, Charlton, Jocelyn, Perotti, Daniela, Radice, Paolo, Geller, James I, Pritchard-Jones, Kathy, Weeks, Mark
Publicado 2014

Chromosomal anomalies at 1q, 3, 16q, and mutations of SIX1 and DROSHA genes underlie Wilms tumor recurrences

por Spreafico, Filippo, Ciceri, Sara, Gamba, Beatrice, Torri, Federica, Terenziani, Monica, Collini, Paola, Macciardi, Fabio, Radice, Paolo, Perotti, Daniela
Publicado 2016

WTX R353X mutation in a family with osteopathia striata and cranial sclerosis (OS-CS): case report and literature review of the disease clinical, genetic and radiological features

por Zicari, Anna Maria, Tarani, Luigi, Perotti, Daniela, Papetti, Laura, Nicita, Francesco, Liberati, Natascia, Spalice, Alberto, Salvatori, Guglielmo, Guaraldi, Federica, Duse, Marzia
Publicado 2012

Possible Role of Pandemic AH1N1 Swine Flu Virus in a Childhood Leukemia Cluster

por Cazzaniga, Giovanni, Bisanti, Luigi, Randi, Giorgia, Deandrea, Silvia, Bungaro, Silvia, Pregliasco, Fabrizio, Perotti, Daniela, Spreafico, Filippo, Masera, Giuseppe, Valsecchi, Maria Grazia, Biondi, Andrea, Greaves, Mel
Publicado 2017

Distinct Methylation Changes at the IGF2-H19 Locus in Congenital Growth Disorders and Cancer

por Murrell, Adele, Ito, Yoko, Verde, Gaetano, Huddleston, Joanna, Woodfine, Kathryn, Silengo, Margherita Cirillo, Spreafico, Filippo, Perotti, Daniela, De Crescenzo, Agostina, Sparago, Angela, Cerrato, Flavia, Riccio, Andrea
Publicado 2008

Gene expression-based dissection of inter-histotypes, intra-histotype and intra-tumor heterogeneity in pediatric tumors

por Ciceri, Sara, Carenzo, Andrea, Iannó, Maria Federica, Bertolotti, Alessia, Morosi, Carlo, Luksch, Roberto, Spreafico, Filippo, Collini, Paola, Radice, Paolo, Massimino, Maura, De Cecco, Loris, Perotti, Daniela
Publicado 2022

Whole transcriptome sequencing identifies BCOR internal tandem duplication as a common feature of clear cell sarcoma of the kidney

por Astolfi, Annalisa, Melchionda, Fraia, Perotti, Daniela, Fois, Maura, Indio, Valentina, Urbini, Milena, Genovese, Chiara Giusy, Collini, Paola, Salfi, Nunzio, Nantron, Marilina, D'Angelo, Paolo, Spreafico, Filippo, Pession, Andrea
Publicado 2015

Quantitative DNA methylation analysis improves epigenotype-phenotype correlations in Beckwith-Wiedemann syndrome

por Calvello, Mariarosaria, Tabano, Silvia, Colapietro, Patrizia, Maitz, Silvia, Pansa, Alessandra, Augello, Claudia, Lalatta, Faustina, Gentilin, Barbara, Spreafico, Filippo, Calzari, Luciano, Perotti, Daniela, Larizza, Lidia, Russo, Silvia, Selicorni, Angelo, Sirchia, Silvia M, Miozzo, Monica
Publicado 2013

Constitutional de novo deletion of the FBXW7 gene in a patient with focal segmental glomerulosclerosis and multiple primitive tumors

por Roversi, Gaia, Picinelli, Chiara, Bestetti, Ilaria, Crippa, Milena, Perotti, Daniela, Ciceri, Sara, Saccheri, Fabiana, Collini, Paola, Poliani, Pietro L., Catania, Serena, Peissel, Bernard, Pagni, Fabio, Russo, Silvia, Peterlongo, Paolo, Manoukian, Siranoush, Finelli, Palma
Publicado 2015

Molecular Signature of Biological Aggressiveness in Clear Cell Sarcoma of the Kidney (CCSK)

por Fiore, Michele, Taddia, Alberto, Indio, Valentina, Bertuccio, Salvatore Nicola, Messelodi, Daria, Serravalle, Salvatore, Bandini, Jessica, Spreafico, Filippo, Perotti, Daniela, Collini, Paola, Di Cataldo, Andrea, Pasquinelli, Gianandrea, Chiarini, Francesca, Fois, Maura, Melchionda, Fraia, Pession, Andrea, Astolfi, Annalisa
Publicado 2023

The UMBRELLA SIOP–RTSG 2016 Wilms tumour pathology and molecular biology protocol

por Vujanić, Gordan M., Gessler, Manfred, Ooms, Ariadne H. A. G., Collini, Paola, Coulomb-l’Hermine, Aurore, D’Hooghe, Ellen, de Krijger, Ronald R., Perotti, Daniela, Pritchard-Jones, Kathy, Vokuhl, Christian, van den Heuvel-Eibrink, Marry M., Graf, Norbert
Publicado 2018

Publisher Correction: The UMBRELLA SIOP–RTSG 2016 Wilms tumour pathology and molecular biology protocol

por Vujanić, Gordan M., Gessler, Manfred, Ooms, Ariadne H. A. G., Collini, Paola, Coulomb-l’Hermine, Aurore, D’Hooghe, Ellen, de Krijger, Ronald R., Perotti, Daniela, Pritchard-Jones, Kathy, Vokuhl, Christian, van den Heuvel-Eibrink, Marry M., Graf, Norbert
Publicado 2019

Genetic and epigenetic analyses guided by high resolution whole-genome SNP array reveals a possible role of CHEK2 in Wilms tumour susceptibility

por Ciceri, Sara, Gamba, Beatrice, Corbetta, Paola, Mondini, Patrizia, Terenziani, Monica, Catania, Serena, Nantron, Marilina, Bianchi, Maurizio, D’Angelo, Paolo, Torri, Federica, Macciardi, Fabio, Collini, Paola, Di Martino, Martina, Melchionda, Fraia, Di Cataldo, Andrea, Spreafico, Filippo, Radice, Paolo, Perotti, Daniela
Publicado 2018

Prognostic Factors for Wilms Tumor Recurrence: A Review of the Literature

por Groenendijk, Alissa, Spreafico, Filippo, de Krijger, Ronald R., Drost, Jarno, Brok, Jesper, Perotti, Daniela, van Tinteren, Harm, Venkatramani, Rajkumar, Godziński, Jan, Rübe, Christian, Geller, James I., Graf, Norbert, van den Heuvel-Eibrink, Marry M., Mavinkurve-Groothuis, Annelies M. C.
Publicado 2021