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The Clinical Spectrum of ANO3-Report of a New Family and Literature Review.
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
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Reply to: "Lack of Association between TWNK Rare Variants and Parkinson's Disease in a Chinese Cohort".
Percetti M, Monfrini E, Caporali L, Minardi R, Carelli V, Valente EM, Di Fonzo A.
Percetti M, et al.
Mov Disord. 2023 Apr;38(4):709-710. doi: 10.1002/mds.29373.
Mov Disord. 2023.
PMID: 37061879
No abstract available.
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Reply to: No Association between Rare TWNK Variants and Parkinson's Disease in European Cohorts.
Percetti M, Monfrini E, Caporali L, Minardi R, Carelli V, Valente EM, Di Fonzo A.
Percetti M, et al.
Mov Disord. 2022 Nov;37(11):2319-2320. doi: 10.1002/mds.29244.
Mov Disord. 2022.
PMID: 36373941
No abstract available.
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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.
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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.
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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
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Childhood-onset dystonia with cerebellar signs: expanding the spectrum of GNAL mutations.
Erro R, Di Fonzo A, Percetti M, Monfrini E, Scannapieco S, Picillo M, Barone P.
Erro R, et al. Among authors: percetti m.
Eur J Neurol. 2020 Nov;27(11):e66-e67. doi: 10.1111/ene.14220. Epub 2020 Apr 3.
Eur J Neurol. 2020.
PMID: 32180288
No abstract available.
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