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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: milesi 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: milesi a. Muscle Nerve. 2012 Jun;45(6):918-9. doi: 10.1002/mus.23265. Muscle Nerve. 2012. PMID: 22581551 No abstract available.
Recurrent transient global amnesia as presenting symptoms of CADASIL.
Pradotto L, Orsi L, Mencarelli M, Caglio M, Lauro D, Milesi A, Di Blasio A, Mauro A. Pradotto L, et al. Among authors: milesi a. Clin Case Rep. 2016 Sep 28;4(11):1045-1048. doi: 10.1002/ccr3.666. eCollection 2016 Nov. Clin Case Rep. 2016. PMID: 27830070 Free PMC article.
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. 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.
28 results