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Therapy in prion diseases.
Forloni G, Artuso V, Roiter I, Morbin M, Tagliavini F. Forloni G, et al. Among authors: roiter i. Curr Top Med Chem. 2013;13(19):2465-76. doi: 10.2174/15680266113136660173. Curr Top Med Chem. 2013. PMID: 24059336 Review.
Preventive pharmacological treatment in subjects at risk for fatal familial insomnia: science and public engagement.
Forloni G, Roiter I, Artuso V, Marcon M, Colesso W, Luban E, Lucca U, Tettamanti M, Pupillo E, Redaelli V, Mariuzzo F, Boscolo Buleghin G, Mariuzzo A, Tagliavini F, Chiesa R, Ambrosini A. Forloni G, et al. Among authors: roiter i. Prion. 2022 Dec;16(1):66-77. doi: 10.1080/19336896.2022.2083435. Prion. 2022. PMID: 35737759 Free PMC article.
[A rare hyperthyroid syndrome].
Artuso V, Roiter I. Artuso V, et al. Among authors: roiter i. Minerva Endocrinol. 2004 Jun;29(2):71-5. Minerva Endocrinol. 2004. PMID: 15257258 Italian.
Presenilin-1 mutation E318G and familial Alzheimer's disease in the Italian population.
Albani D, Roiter I, Artuso V, Batelli S, Prato F, Pesaresi M, Galimberti D, Scarpini E, Bruni A, Franceschi M, Piras MR, Confaloni A, Forloni G. Albani D, et al. Among authors: roiter i. Neurobiol Aging. 2007 Nov;28(11):1682-8. doi: 10.1016/j.neurobiolaging.2006.07.003. Epub 2006 Sep 6. Neurobiol Aging. 2007. PMID: 16952411
Age at onset in genetic prion disease and the design of preventive clinical trials.
Minikel EV, Vallabh SM, Orseth MC, Brandel JP, Haïk S, Laplanche JL, Zerr I, Parchi P, Capellari S, Safar J, Kenny J, Fong JC, Takada LT, Ponto C, Hermann P, Knipper T, Stehmann C, Kitamoto T, Ae R, Hamaguchi T, Sanjo N, Tsukamoto T, Mizusawa H, Collins SJ, Chiesa R, Roiter I, de Pedro-Cuesta J, Calero M, Geschwind MD, Yamada M, Nakamura Y, Mead S. Minikel EV, et al. Among authors: roiter i. Neurology. 2019 Jul 9;93(2):e125-e134. doi: 10.1212/WNL.0000000000007745. Epub 2019 Jun 6. Neurology. 2019. PMID: 31171647 Free PMC article.
38 results