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Psychosocial burden and professional and social support in patients with hereditary transthyretin amyloidosis (ATTRv) and their relatives in Italy.
Magliano L, Obici L, Sforzini C, Mazzeo A, Russo M, Cappelli F, Fenu S, Luigetti M, Tagliapietra M, Gemelli C, Leonardi L, Tozza S, Pradotto LG, Citarelli G, Mauro A, Manganelli F, Antonini G, Grandis M, Fabrizi GM, Sabatelli M, Pareyson D, Perfetto F, Merlini G, Vita G; ATTRv Collaborators. Magliano L, et al. Among authors: mauro a. Orphanet J Rare Dis. 2021 Apr 7;16(1):163. doi: 10.1186/s13023-021-01812-6. Orphanet J Rare Dis. 2021. PMID: 33827635 Free PMC article.
A new NOTCH3 mutation presenting as primary intracerebral haemorrhage.
Pradotto L, Orsi L, Daniele D, Caroppo P, Lauro D, Milesi A, Sellitti L, Mauro A. Pradotto L, et al. Among authors: mauro a. J Neurol Sci. 2012 Apr 15;315(1-2):143-5. doi: 10.1016/j.jns.2011.12.003. Epub 2011 Dec 27. J Neurol Sci. 2012. PMID: 22206696
Amyloid polyneuropathy following domino liver transplantation.
Pradotto L, Franchello A, Milesi A, Romagnoli R, Bigoni M, Vigna L, Di Sapio A, Salizzoni M, Mauro A. Pradotto L, et al. Among authors: mauro a. Muscle Nerve. 2012 Jun;45(6):918-9. doi: 10.1002/mus.23265. Muscle Nerve. 2012. PMID: 22581551 No abstract available.
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 GM, Schenone A, Grandis M, Gemelli C, Mauro A, Pradotto LG, Gentile L, Stancanelli C, Lozza A, Perlini S, Piscosquito G, Calabrese D, Mazzeo A, Obici L, Pareyson D. Cortese A, et al. Among authors: mauro a. J Neurol. 2016 May;263(5):916-924. doi: 10.1007/s00415-016-8064-9. Epub 2016 Mar 16. J Neurol. 2016. PMID: 26984605
952 results