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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: artuso v. 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
Therapy in prion diseases.
Forloni G, Artuso V, Roiter I, Morbin M, Tagliavini F. Forloni G, et al. Among authors: artuso v. 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: artuso v. 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. Minerva Endocrinol. 2004 Jun;29(2):71-5. Minerva Endocrinol. 2004. PMID: 15257258 Italian.
14 results