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

par STRIPPOLI, SABINO, TRAVERSA, MICHELE, CRAMAROSSA, ANTONIO, POPESCU, ONDINA, LORUSSO, VITO, GUIDA, MICHELE
Publié dans Oncol Lett (2015)

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

par Abeni, Edoardo, Salvi, Alessandro, Marchina, Eleonora, Traversa, Michele, Arici, Bruna, De Petro, Giuseppina
Publié dans 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

par Magri, Chiara, Marchina, Eleonora, Bertini, Valeria, Traversa, Michele, Savio, Giulia, Pilotta, Alba, Piovani, Giovanna
Publié dans BMC Med Genet (2015)

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

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

New Copy Number Variations in Schizophrenia

par Magri, Chiara, Sacchetti, Emilio, Traversa, Michele, Valsecchi, Paolo, Gardella, Rita, Bonvicini, Cristian, Minelli, Alessandra, Gennarelli, Massimo, Barlati, Sergio
Publié 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...

par Ritelli, Marco, Chiarelli, Nicola, Zoppi, Nicoletta, Dordoni, Chiara, Quinzani, Stefano, Traversa, Michele, Venturini, Marina, Calzavara-Pinton, Piergiacomo, Colombi, Marina
Publié dans 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

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

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

par 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
Publié 2013

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

par 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
Publié dans Cancers (Basel) (2019)