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NOTCH3 gene mutations in subjects clinically suspected of CADASIL.
Mosca L, Marazzi R, Ciccone A, Santilli I, Bersano A, Sansone V, Grosso E, Mandrile G, Giachino DF, Adobbati L, Corengia E, Agostoni E, Fiumani A, Gallone S, Scarpini E, Guidotti M, Sterzi R, Ajmone C, Marocchi A, Penco S. Mosca L, et al. Among authors: sansone v. J Neurol Sci. 2011 Aug 15;307(1-2):144-8. doi: 10.1016/j.jns.2011.04.019. Epub 2011 May 26. J Neurol Sci. 2011. PMID: 21616505 Free article.
ALS Cognitive Behavioral Screen (ALS-CBS): normative values for the Italian population and clinical usability.
Tremolizzo L, Lizio A, Santangelo G, Diamanti S, Lunetta C, Gerardi F, Messina S, La Foresta S, Riva N, Falzone Y, Filippi M, Woolley SC, Sansone VA, Siciliano M, Ferrarese C, Appollonio I; ALS-CBS Italian Study Group. Tremolizzo L, et al. Neurol Sci. 2020 Apr;41(4):835-841. doi: 10.1007/s10072-019-04154-1. Epub 2019 Dec 5. Neurol Sci. 2020. PMID: 31807998
Burden of Rare Variants in ALS and Axonal Hereditary Neuropathy Genes Influence Survival in ALS: Insights from a Next Generation Sequencing Study of an Italian ALS Cohort.
Scarlino S, Domi T, Pozzi L, Romano A, Pipitone GB, Falzone YM, Mosca L, Penco S, Lunetta C, Sansone V, Tremolizzo L, Fazio R, Agosta F, Filippi M, Carrera P, Riva N, Quattrini A. Scarlino S, et al. Among authors: sansone v. Int J Mol Sci. 2020 May 8;21(9):3346. doi: 10.3390/ijms21093346. Int J Mol Sci. 2020. PMID: 32397312 Free PMC article.
Proximal myotonic myopathy: a syndrome with a favourable prognosis?
Meola G, Sansone V, Marinou K, Cotelli M, Moxley RT 3rd, Thornton CA, De Ambroggi L. Meola G, et al. Among authors: sansone v. J Neurol Sci. 2002 Jan 15;193(2):89-96. doi: 10.1016/s0022-510x(01)00649-9. J Neurol Sci. 2002. PMID: 11790388
378 results