PhD Programme in Experimental Medicine and Therapy - Dottorato in Medicina e Terapia Sperimentale

[1]Solaro C, Schenone A, Di Sapio A, Pradotto L, Mancardi GL, Primavera A, Mauro A. An Italian family with Ala-47 transthyretin mutation associated with cardiomyopathy and polyneuropathy. Neuromuscular Disorders. 2000;10(1):52–5.

[2]Giordana MT, Duó D, Gasverde S, Trevisan E, Boghi A, Morra I, Pradotto L, Mauro A, Chiò A. MDM2 overexpression is associated with short survival in adults with medulloblastoma. Neuro-Oncology. 2002;4(2):115–22.

[3]Di Sapio A, Morra I, Pradotto L, Guido M, Schiffer D, Mauro A. Molecular genetic changes in a series of neuroepithelial tumors of childhood. Journal of Neuro-Oncology. 2002;59(2):117–22.

[4]Mauro A, Pradotto L. Neuropatie amiloidotiche. Notiziario cardiologico e medico. 2004;17(5):4-8.

[5]Pradotto L, Azan G, Doriguzzi C, Valentini C, Mauro A. Sporadic vascular dementia as clinical presentation of a new missense mutation within exon 7 of NOTCH3 gene. Journal of the Neurological Sciences. 2008;271(1-2):207–10.

[6]Brussino A, Vaula G, Cagnoli C, Mauro A, Pradotto L, Daniele D, Di Gregorio E, Barberis M, Arduino C, Squadrone S, Abete MC, Migone N, Calabrese O, Brusco A. A novel family with Lamin B1 duplication associated with adult-onset leucoencephalopathy. Journal of Neurology, Neurosurgery and Psychiatry. 2009;80(2):237–40.

[7]Brioschi AM, Calderoni S, Pradotto LG, Guido M, Strada A, Zenga F, Benech CA, Benech F, Serpe L, Zara GP, Musicanti C, Ducati A, Gasco MR, Mauro A. Solid lipid nanoparticles carrying oligonucleotides inhibit vascular endothelial growth factor expression in rat glioma models. Journal of Nanoneuroscience. 2009;1(1):65–74.

[8]Priano L, Giaccone G, Mangieri M, Albani G, Limido L, Brioschi A, Pradotto L, Orsi L, Mortara P, Fociani P, Mauro A, Tagliavini F. An atypical case of sporadic fatal insomnia. Journal of Neurology, Neurosurgery and Psychiatry. 2009;80(8):924–7.

[9]Albani G, El Assawy N, Cattaldo S, De Gennaro M, Gregorini F, Pradotto L, Mauro A. Electrogastrographyc activity in Parkinson’s disease patients with and without motor fluctuations. Movement Disorders. 2011;26(9):1737–40.

[10]      Pradotto L, Orsi L, Daniele D, Caroppo P, Lauro D, Milesi A, Sellitti L, Mauro A. A new Notch3 mutation presenting as primary intracerebral haemorrhage. Journal of the Neurological Sciences. 2012;315:143–145.

[11]      Pradotto L, Franchello A, Milesi A, Romagnoli R, Bigoni M, Vigna L, Di Sapio A, Salizzoni M, Mauro A. Amyloid polyneuropathy following domino liver transplantation. Muscle and Nerve. 2012;45:918-919.

[12]      Testi S, Malerba G, Ferrarini M, Ragno M, Pradotto L, Mauro A, Fabrizi GM. Mutational and haplotype map of NOTCH3 in a cohort of Italian patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL). Journal of the Neurological Sciences. 2012;319:37-41.

[13]      Marconi R, Antonini A, Barone P, Colosimo C, Avarello TP, Bottacchi E, Cannas A, Ceravolo MG, Ceravolo R, Cicarelli G, Gaglio RM, Giglia L, Iemolo F, Manfredi M, Meco G, Nicoletti A, Pederzoli M, Petrone A, Pisani A, Pontieri FE, Quatrale R, Ramat S, Scala R, Volpe G, Zappulla S, Bentivoglio AR, Stocchi F, Trianni G, Del Dotto P, De Gaspari D, Grasso L, Morgante F, Santangelo G, Fabbrini G, Morgante L, PRIAMO study group. Frontal assessment battery scores and non-motor symptoms in parkinsonian disorders. Neurological Sciences. 2012;33:585-93.

[14]      Galeotti F, Massari M, D’Alessandro R. Beghi E, Chio` A, Logroscino G, Filippini G, Benedetti MD, Pugliatti M, Santuccio C, Raschetti R, The ITANG study group. Risk of Guillain-Barre´ syndrome after 2010–2011 influenza vaccination. European Journal of Epidemiology. 2013;28:433–444.