Detection of the (11;22)(q24;q12) translocation of Ewing's sarcoma and peripheral neuroectodermal tumor by reverse transcription polymerase chain reaction.

Por Downing, J. R., Head, D. R., Parham, D. M., Douglass, E. C., Hulshof, M. G., Link, M. P., Motroni, T. A., Grier, H. E., Curcio-Brint, A. M., Shapiro, D. N.
Publicado em 1993

Homozygous carriers of APP A713T mutation in an autosomal dominant Alzheimer disease family

Por Conidi, Maria E., Bernardi, Livia, Puccio, Gianfranco, Smirne, Nicoletta, Muraca, Maria G., Curcio, Sabrina A.M., Colao, Rosanna, Piscopo, Paola, Gallo, Maura, Anfossi, Maria, Frangipane, Francesca, Clodomiro, Alessandra, Mirabelli, Maria, Vasso, Franca, Cupidi, Chiara, Torchia, Giusi, Di Lorenzo, Raffaele, Mandich, Paola, Confaloni, Annamaria, Maletta, Raffaele G., Bruni, Amalia C.
Publicado no Neurology (2015)

Mutation analysis of CHCHD10 in different neurodegenerative diseases

Por Zhang, Ming, Xi, Zhengrui, Zinman, Lorne, Bruni, Amalia C., Maletta, Raffaele G., Curcio, Sabrina A. M., Rainero, Innocenzo, Rubino, Elisa, Pinessi, Lorenzo, Nacmias, Benedetta, Sorbi, Sandro, Galimberti, Daniela, Lang, Anthony E., Fox, Susan, Surace, Ezequiel I., Ghani, Mahdi, Guo, Jing, Sato, Christine, Moreno, Danielle, Liang, Yan, Keith, Julia, Traynor, Bryan J., St George-Hyslop, Peter, Rogaeva, Ekaterina
Publicado no Brain (2015)

Worldwide distribution of PSEN1 Met146Leu mutation: A large variability for a founder mutation

Por Bruni, A. C., Bernardi, L., Colao, R., Rubino, E., Smirne, N., Frangipane, F., Terni, B., Curcio, S.A.M., Mirabelli, M., Clodomiro, A., Di Lorenzo, R., Maletta, R., Anfossi, M., Gallo, M., Geracitano, S., Tomaino, C., Muraca, M. G., Leotta, A., Lio, S. G., Pinessi, L., Rainero, I., Sorbi, S., Nee, L., Milan, G., Pappatá, S., Postiglione, A., Abbamondi, N., Forloni, G., St. George Hyslop, P., Rogaeva, E., Bugiani, O., Giaccone, G., Foncin, J. F., Spillantini, M. G., Puccio, G.
Publicado em 2010