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The Clinical Spectrum of ANO3-Report of a New Family and Literature Review.
Percetti M, Zini M, Soliveri P, Cogiamanian F, Ferrara M, Orunesu E, Ranghetti A, Ferrarese C, Pezzoli G, Garavaglia B, Isaias IU, Sacilotto G. Percetti M, et al. Among authors: pezzoli g. Mov Disord Clin Pract. 2024 Mar;11(3):289-297. doi: 10.1002/mdc3.13979. Epub 2024 Jan 29. Mov Disord Clin Pract. 2024. PMID: 38284143 Review.
Systematic rare variant analyses identify RAB32 as a susceptibility gene for familial Parkinson's disease.
Hop PJ, Lai D, Keagle PJ, Baron DM, Kenna BJ, Kooyman M, Shankaracharya, Halter C, Straniero L, Asselta R, Bonvegna S, Soto-Beasley AI; Project MinE ALS Sequencing Consortium; Wszolek ZK, Uitti RJ, Isaias IU, Pezzoli G, Ticozzi N, Ross OA, Veldink JH, Foroud TM, Kenna KP, Landers JE. Hop PJ, et al. Among authors: pezzoli g. Nat Genet. 2024 Jul;56(7):1371-1376. doi: 10.1038/s41588-024-01787-7. Epub 2024 Jun 10. Nat Genet. 2024. PMID: 38858457 Free PMC article.
Optimal MMSE and MoCA cutoffs for cognitive diagnoses in Parkinson's disease: A data-driven decision tree model.
Fiorenzato E, Cauzzo S, Weis L, Garon M, Pistonesi F, Cianci V, Nasi ML, Vianello F, Zecchinelli AL, Pezzoli G, Reali E, Pozzi B, Isaias IU, Siri C, Santangelo G, Cuoco S, Barone P, Antonini A, Biundo R. Fiorenzato E, et al. Among authors: pezzoli g. J Neurol Sci. 2024 Nov 15;466:123283. doi: 10.1016/j.jns.2024.123283. Epub 2024 Oct 22. J Neurol Sci. 2024. PMID: 39471638
377 results