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

Por STRIPPOLI, SABINO, TRAVERSA, MICHELE, CRAMAROSSA, ANTONIO, POPESCU, ONDINA, LORUSSO, VITO, GUIDA, MICHELE
Publicado no Oncol Lett (2015)

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

Por Abeni, Edoardo, Salvi, Alessandro, Marchina, Eleonora, Traversa, Michele, Arici, Bruna, De Petro, Giuseppina
Publicado no 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

Por Magri, Chiara, Marchina, Eleonora, Bertini, Valeria, Traversa, Michele, Savio, Giulia, Pilotta, Alba, Piovani, Giovanna
Publicado no BMC Med Genet (2015)

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

Por Piovani, Giovanna, Savio, Giulia, Traversa, Michele, Pilotta, Alba, De Petro, Giuseppina, Barlati, Sergio, Magri, Chiara
Publicado em 2014

New Copy Number Variations in Schizophrenia

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

Por Ritelli, Marco, Chiarelli, Nicola, Zoppi, Nicoletta, Dordoni, Chiara, Quinzani, Stefano, Traversa, Michele, Venturini, Marina, Calzavara-Pinton, Piergiacomo, Colombi, Marina
Publicado no 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

Por Giacopuzzi, Edoardo, Gennarelli, Massimo, Minelli, Alessandra, Gardella, Rita, Valsecchi, Paolo, Traversa, Michele, Bonvicini, Cristian, Vita, Antonio, Sacchetti, Emilio, Magri, Chiara
Publicado no PLoS One (2017)

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

Por 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
Publicado em 2013

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

Por 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
Publicado no Cancers (Basel) (2019)