Long-term response of gemcitabine plus docetaxel chemotherapy regimen for extraskeletal osteosarcoma: A case report

di STRIPPOLI, SABINO, TRAVERSA, MICHELE, CRAMAROSSA, ANTONIO, POPESCU, ONDINA, LORUSSO, VITO, GUIDA, MICHELE
Pubblicato in Oncol Lett (2015)

Sorafenib induces variations of the DNA methylome in HA22T/VGH human hepatocellular carcinoma-derived cells

di Abeni, Edoardo, Salvi, Alessandro, Marchina, Eleonora, Traversa, Michele, Arici, Bruna, De Petro, Giuseppina
Pubblicato in Int J Oncol (2017)

SNP array and FISH analysis of a proband with a 22q13.2- 22qter duplication shed light on the molecular origin of the rearrangement

di Magri, Chiara, Marchina, Eleonora, Bertini, Valeria, Traversa, Michele, Savio, Giulia, Pilotta, Alba, Piovani, Giovanna
Pubblicato in BMC Med Genet (2015)

De novo 1Mb interstitial deletion of 8p22 in a patient with slight mental retardation and speech delay

di Piovani, Giovanna, Savio, Giulia, Traversa, Michele, Pilotta, Alba, De Petro, Giuseppina, Barlati, Sergio, Magri, Chiara
Pubblicazione 2014

New Copy Number Variations in Schizophrenia

di Magri, Chiara, Sacchetti, Emilio, Traversa, Michele, Valsecchi, Paolo, Gardella, Rita, Bonvicini, Cristian, Minelli, Alessandra, Gennarelli, Massimo, Barlati, Sergio
Pubblicazione 2010

Insights in the etiopathology of galactosyltransferase II (GalT-II) deficiency from transcriptome-wide expression profiling of skin fibroblasts of two sisters with compound heteroz...

di Ritelli, Marco, Chiarelli, Nicola, Zoppi, Nicoletta, Dordoni, Chiara, Quinzani, Stefano, Traversa, Michele, Venturini, Marina, Calzavara-Pinton, Piergiacomo, Colombi, Marina
Pubblicato in Mol Genet Metab Rep (2014)

Exome sequencing in schizophrenic patients with high levels of homozygosity identifies novel and extremely rare mutations in the GABA/glutamatergic pathways

di Giacopuzzi, Edoardo, Gennarelli, Massimo, Minelli, Alessandra, Gardella, Rita, Valsecchi, Paolo, Traversa, Michele, Bonvicini, Cristian, Vita, Antonio, Sacchetti, Emilio, Magri, Chiara
Pubblicato in PLoS One (2017)

Clinical and molecular characterization of 40 patients with classic Ehlers–Danlos syndrome: identification of 18 COL5A1 and 2 COL5A2 novel mutations

di Ritelli, Marco, Dordoni, Chiara, Venturini, Marina, Chiarelli, Nicola, Quinzani, Stefano, Traversa, Michele, Zoppi, Nicoletta, Vascellaro, Annalisa, Wischmeijer, Anita, Manfredini, Emanuela, Garavelli, Livia, Calzavara-Pinton, Piergiacomo, Colombi, Marina
Pubblicazione 2013

The Management of Oligoprogression in the Landscape of New Therapies for Metastatic Melanoma

di Guida, Michele, Bartolomeo, Nicola, De Risi, Ivana, Fucci, Livia, Armenio, Andrea, Filannino, Ruggero, Ruggieri, Eustachio, Macina, Francesco, Traversa, Michele, Nardone, Annalisa, Figliuolo, Francesco, De Luca, Federica, Mele, Fabio, Tommasi, Stefania, Strippoli, Sabino
Pubblicato in Cancers (Basel) (2019)