Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

Search Results

8 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Results By Year timeline is not available.
Page 1
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. 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.
Harmonizing Genetic Testing for Parkinson's Disease: Results of the PARKNET Multicentric Study.
Di Fonzo A, Percetti M, Monfrini E, Palmieri I, Albanese A, Avenali M, Bartoletti-Stella A, Blandini F, Brescia G, Calandra-Buonaura G, Campopiano R, Capellari S, Colangelo I, Comi GP, Cuconato G, Ferese R, Galandra C, Gambardella S, Garavaglia B, Gaudio A, Giardina E, Invernizzi F, Mandich P, Mineri R, Panteghini C, Reale C, Trevisan L, Zampatti S, Cortelli P, Valente EM; PARKNET study group. Di Fonzo A, et al. Among authors: percetti m. Mov Disord. 2023 Dec;38(12):2241-2248. doi: 10.1002/mds.29617. Epub 2023 Sep 26. Mov Disord. 2023. PMID: 37750340
TWNK in Parkinson's Disease: A Movement Disorder and Mitochondrial Disease Center Perspective Study.
Percetti M, Franco G, Monfrini E, Caporali L, Minardi R, La Morgia C, Valentino ML, Liguori R, Palmieri I, Ottaviani D, Vizziello M, Ronchi D, Di Berardino F, Cocco A, Macao B, Falkenberg M, Comi GP, Albanese A, Giometto B, Valente EM, Carelli V, Di Fonzo A. Percetti M, et al. Mov Disord. 2022 Sep;37(9):1938-1943. doi: 10.1002/mds.29139. Epub 2022 Jul 6. Mov Disord. 2022. PMID: 35792653 Free PMC article.
VPS13C-associated Parkinson's disease: Two novel cases and review of the literature.
Monfrini E, Spagnolo F, Canesi M, Seresini A, Rini A, Passarella B, Percetti M, Seia M, Goldwurm S, Cereda V, Comi GP, Pezzoli G, Di Fonzo A. Monfrini E, et al. Among authors: percetti m. Parkinsonism Relat Disord. 2022 Jan;94:37-39. doi: 10.1016/j.parkreldis.2021.11.031. Epub 2021 Dec 1. Parkinsonism Relat Disord. 2022. PMID: 34875562 Review.
Screening of LRP10 mutations in Parkinson's disease patients from Italy.
Manini A, Straniero L, Monfrini E, Percetti M, Vizziello M, Franco G, Rimoldi V, Zecchinelli A, Pezzoli G, Corti S, Comi GP, Duga S, Di Fonzo A. Manini A, et al. Among authors: percetti m. Parkinsonism Relat Disord. 2021 Aug;89:17-21. doi: 10.1016/j.parkreldis.2021.06.014. Epub 2021 Jun 19. Parkinsonism Relat Disord. 2021. PMID: 34216936