Recommendations for pre-symptomatic genetic testing for hereditary transthyretin amyloidosis in the era of effective therapy: a multicenter Italian consensus by Grandis, M, Obici, L, Luigetti, M, Briani, C, Benedicenti, F, Bisogni, G, Canepa, M, Cappelli, F, Danesino, C, Fabrizi, G M, Fenu, S, Ferrandes, G, Gemelli, C, Manganelli, F, Mazzeo, A, Melchiorri, L, Perfetto, F, Pradotto, L G, Rimessi, P, Tini, G, Tozza, S, Trevisan, L, Pareyson, D, Mandich, P

Get full text

Monitoring effectiveness and safety of Tafamidis in transthyretin amyloidosis in Italy: a longitudinal multicenter study in a non-endemic area by Cortese, A., Vita, G., Luigetti, M., Russo, M., Bisogni, G., Sabatelli, M., Manganelli, F., Santoro, L., Cavallaro, T., Fabrizi, G. M., Schenone, A., Grandis, M., Gemelli, C., Mauro, A., Pradotto, L. G., Gentile, L., Stancanelli, C., Lozza, A., Perlini, S., Piscosquito, G., Calabrese, D., Mazzeo, A., Obici, L., Pareyson, D.

Get full text

Mutational and haplotype map of NOTCH3 in a cohort of Italian patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) by Testi, S, Malerba, G, Ferrarini, M, Ragno, M, Pradotto, L, Mauro, A, Fabrizi, G.M

Get full text

Erratum to: Monitoring effectiveness and safety of Tafamidis in transthyretin amyloidosis in Italy: a longitudinal multicenter study in a non-endemic area by Cortese, A., Vita, G., Luigetti, M., Russo, M., Bisogni, G., Sabatelli, M., Manganelli, F., Santoro, L., Cavallaro, T., Fabrizi, G. M., Schenone, A., Grandis, M., Gemelli, C., Mauro, A., Pradotto, L. G., Gentile, L., Stancanelli, C., Lozza, A., Perlini, S., Piscosquito, G., Calabrese, D., Mazzeo, A., Obici, L., Pareyson, D.

Get full text

Sporadic vascular dementia as clinical presentation of a new missense mutation within exon 7 of NOTCH3 gene by Pradotto, L, Azan, G, Doriguzzi, C, Valentini, C, Mauro, A

Get full text

P1.021 Executive functions in a virtual world: a study in Parkinson's disease by Albani, G, Riva, G, Raspelli, S, Pradotto, L, Pignatti, R, Mauro, A

Get full text

An Italian family with Ala-47 transthyretin mutation associated with cardiomyopathy and polyneuropathy by Solaro, C, Schenone, A, Di Sapio, A, Pradotto, L, Mancardi, G L, Primavera, A, Mauro, A

Get full text

Frontal assessment battery scores and non-motor symptoms in parkinsonian disorders by Marconi, Roberto, Antonini, Angelo, Barone, Paolo, Colosimo, Carlo, Avarello, Tania P., Bottacchi, Edo, Cannas, Antonino, Ceravolo, Maria G., Ceravolo, Roberto, Cicarelli, Giulio, Gaglio, Rosa M., Giglia, Luisa, Iemolo, Francesco, Manfredi, Michela, Meco, Giuseppe, Nicoletti, Alessandra, Pederzoli, Massimo, Petrone, Alfredo, Pisani, Antonio, Pontieri, Francesco E., Quatrale, Rocco, Ramat, Silvia, Scala, Rossana, Volpe, Giampiero, Zappulla, Salvatore, Bentivoglio, Anna Rita, Stocchi, Fabrizio, Trianni, Giorgio, Del Dotto, Paolo, De Gaspari, Danilo, Grasso, Lucia, Morgante, Francesca, Santangelo, Gabriella, Fabbrini, Giovanni, Morgante, Letterio

Get full text

Molecular genetic changes in a series of neuroepithelial tumors of childhood by DI SAPIO, Alessia, MORRA, Isabella, PRADOTTO, Luca, GUIDO, Marilena, SCHIFFER, Davide, MAURO, Alessandro

Get full text

Abstract P3-12-06: Saving in clinical trials: A possible challenge for improving health care for breast cancer patients by Taverniti, C, Bonfadini, C, Pradotto, M, Cagnazzo, C, Demartini, P, Rossi, L, Ignazzi, G, Arizio, F, Beano, A

Get full text

P2.09-003 Dissecting the Immune Environment in Malignant Pleural Mesothelioma: Results from a Prospective Assessment by Riganti, C., Pradotto, M., Righi, L., Marchiò, C., Capelletto, E., Buttigliero, C., Costardi, L., Kopecka, J., Bironzo, P., Ruffini, E., Novello, S., Scagliotti, G.

Get full text