Recommendations for pre-symptomatic genetic testing for hereditary transthyretin amyloidosis in the era of effective therapy: a multicenter Italian consensus
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
Published in Orphanet journal of rare diseases (14.12.2020)
Published in Orphanet journal of rare diseases (14.12.2020)
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Monitoring effectiveness and safety of Tafamidis in transthyretin amyloidosis in Italy: a longitudinal multicenter study in a non-endemic area
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.
Published in Journal of neurology (01.05.2016)
Published in Journal of neurology (01.05.2016)
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Prevalence and phenotype of the c.1529C>T SPG7 variant in adult‐onset cerebellar ataxia in Italy
Mancini, C., Giorgio, E., Rubegni, A., Pradotto, L., Bagnoli, S., Rubino, E., Prontera, P., Cavalieri, S., Di Gregorio, E., Ferrero, M., Pozzi, E., Riberi, E., Ferrero, P., Nigro, P., Mauro, A., Zibetti, M., Tessa, A., Barghigiani, M., Antenora, A., Sirchia, F., Piacentini, S., Silvestri, G., De Michele, G., Filla, A., Orsi, L., Santorelli, F. M., Brusco, A.
Published in European journal of neurology (01.01.2019)
Published in European journal of neurology (01.01.2019)
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Mutational and haplotype map of NOTCH3 in a cohort of Italian patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)
Testi, S, Malerba, G, Ferrarini, M, Ragno, M, Pradotto, L, Mauro, A, Fabrizi, G.M
Published in Journal of the neurological sciences (15.08.2012)
Published in Journal of the neurological sciences (15.08.2012)
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Erratum to: Monitoring effectiveness and safety of Tafamidis in transthyretin amyloidosis in Italy: a longitudinal multicenter study in a non-endemic area
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.
Published in Journal of neurology (01.05.2016)
Published in Journal of neurology (01.05.2016)
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A novel family with Lamin B1 duplication associated with adult-onset leucoencephalopathy
Brussino, A, Vaula, G, Cagnoli, C, Mauro, A, Pradotto, L, Daniele, D, Di Gregorio, E, Barberis, M, Arduino, C, Squadrone, S, Abete, M C, Migone, N, Calabrese, O, Brusco, A
Published in Journal of neurology, neurosurgery and psychiatry (01.02.2009)
Published in Journal of neurology, neurosurgery and psychiatry (01.02.2009)
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Sporadic vascular dementia as clinical presentation of a new missense mutation within exon 7 of NOTCH3 gene
Pradotto, L, Azan, G, Doriguzzi, C, Valentini, C, Mauro, A
Published in Journal of the neurological sciences (15.08.2008)
Published in Journal of the neurological sciences (15.08.2008)
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An atypical case of sporadic fatal insomnia
Priano, L, Giaccone, G, Mangieri, M, Albani, G, Limido, L, Brioschi, A, Pradotto, L, Orsi, L, Mortara, P, Fociani, P, Mauro, A, Tagliavini, F
Published in Journal of neurology, neurosurgery and psychiatry (01.08.2009)
Published in Journal of neurology, neurosurgery and psychiatry (01.08.2009)
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P1.021 Executive functions in a virtual world: a study in Parkinson's disease
Albani, G, Riva, G, Raspelli, S, Pradotto, L, Pignatti, R, Mauro, A
Published in Parkinsonism & related disorders (2009)
Published in Parkinsonism & related disorders (2009)
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An Italian family with Ala-47 transthyretin mutation associated with cardiomyopathy and polyneuropathy
Solaro, C, Schenone, A, Di Sapio, A, Pradotto, L, Mancardi, G L, Primavera, A, Mauro, A
Published in Neuromuscular disorders : NMD (01.01.2000)
Published in Neuromuscular disorders : NMD (01.01.2000)
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Journal Article
Prevalence and phenotype of the c.1529C>T SPG 7 variant in adult‐onset cerebellar ataxia in Italy
Mancini, C., Giorgio, E., Rubegni, A., Pradotto, L., Bagnoli, S., Rubino, E., Prontera, P., Cavalieri, S., Di Gregorio, E., Ferrero, M., Pozzi, E., Riberi, E., Ferrero, P., Nigro, P., Mauro, A., Zibetti, M., Tessa, A., Barghigiani, M., Antenora, A., Sirchia, F., Piacentini, S., Silvestri, G., De Michele, G., Filla, A., Orsi, L., Santorelli, F. M., Brusco, A.
Published in European journal of neurology (01.01.2019)
Published in European journal of neurology (01.01.2019)
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Molecular genetic changes in a series of neuroepithelial tumors of childhood
DI SAPIO, Alessia, MORRA, Isabella, PRADOTTO, Luca, GUIDO, Marilena, SCHIFFER, Davide, MAURO, Alessandro
Published in Journal of neuro-oncology (01.09.2002)
Published in Journal of neuro-oncology (01.09.2002)
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