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Page 1
Cognitive and Autonomic Dysfunction in Multiple System Atrophy Type P and C: A Comparative Study.
Lazzeri G, Franco G, Difonzo T, Carandina A, Gramegna C, Vergari M, Arienti F, Naci A, Scatà C, Monfrini E, Dias Rodrigues G, Montano N, Comi GP, Saetti MC, Tobaldini E, Di Fonzo A. Lazzeri G, et al. Among authors: comi gp. Front Neurol. 2022 Jun 16;13:912820. doi: 10.3389/fneur.2022.912820. eCollection 2022. Front Neurol. 2022. PMID: 35785342 Free PMC article.
The Length of SNCA Rep1 Microsatellite May Influence Cognitive Evolution in Parkinson's Disease.
Corrado L, De Marchi F, Tunesi S, Oggioni GD, Carecchio M, Magistrelli L, Tesei S, Riboldazzi G, Di Fonzo A, Locci C, Trezzi I, Zangaglia R, Cereda C, D'Alfonso S, Magnani C, Comi GP, Bono G, Pacchetti C, Cantello R, Goldwurm S, Comi C. Corrado L, et al. Among authors: comi gp, comi c. Front Neurol. 2018 Mar 29;9:213. doi: 10.3389/fneur.2018.00213. eCollection 2018. Front Neurol. 2018. PMID: 29662465 Free PMC article.
Clinical features and disease course of patients with acute ischaemic stroke just before the Italian index case: Was COVID-19 already there?
Pietroboni AM, Lanfranconi S, Novella A, Carandini T, Arighi A, Abati E, Brusa R, Costamagna G, Lazzeri G, Mauri E, Pozzato M, Sacchi L, Valcamonica G, Villa D, Bonato S, Comi GP, Bresolin N, Galimberti D, Scarpini E, Nobili A; Neurology-COVID-19 Group. Pietroboni AM, et al. Among authors: comi gp. Intern Emerg Med. 2021 Aug;16(5):1247-1252. doi: 10.1007/s11739-021-02634-x. Epub 2021 Feb 10. Intern Emerg Med. 2021. PMID: 33565035 Free PMC article.
Mitochondrial dysfunction in fibroblasts of Multiple System Atrophy.
Monzio Compagnoni G, Kleiner G, Bordoni A, Fortunato F, Ronchi D, Salani S, Guida M, Corti C, Pichler I, Bergamini C, Fato R, Pellecchia MT, Vallelunga A, Del Sorbo F, Elia A, Reale C, Garavaglia B, Mora G, Albanese A, Cogiamanian F, Ardolino G, Bresolin N, Corti S, Comi GP, Quinzii CM, Di Fonzo A. Monzio Compagnoni G, et al. Among authors: comi gp. Biochim Biophys Acta Mol Basis Dis. 2018 Dec;1864(12):3588-3597. doi: 10.1016/j.bbadis.2018.09.018. Epub 2018 Sep 19. Biochim Biophys Acta Mol Basis Dis. 2018. PMID: 30254015 Free article.
SLC25A46 mutations in patients with Parkinson's Disease and optic atrophy.
Bitetto G, Malaguti MC, Ceravolo R, Monfrini E, Straniero L, Morini A, Di Giacopo R, Frosini D, Palermo G, Biella F, Ronchi D, Duga S, Taroni F, Corti S, Comi GP, Bresolin N, Giometto B, Di Fonzo A. Bitetto G, et al. Among authors: comi gp. Parkinsonism Relat Disord. 2020 May;74:1-5. doi: 10.1016/j.parkreldis.2020.03.018. Epub 2020 Apr 2. Parkinsonism Relat Disord. 2020. PMID: 32259769 Free 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: comi gp. 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.
Mutations in TMEM230 are rare in autosomal dominant Parkinson's disease.
Buongarzone G, Monfrini E, Franco G, Trezzi I, Borellini L, Frattini E, Melzi V, Di Caprio AC, Ronchi D, Monzio Compagnoni G, Cogiamanian F, Ardolino G, Bresolin N, Comi GP, Corti S, Di Fonzo A. Buongarzone G, et al. Among authors: comi gp. Parkinsonism Relat Disord. 2017 Jun;39:87-88. doi: 10.1016/j.parkreldis.2017.03.007. Epub 2017 Mar 9. Parkinsonism Relat Disord. 2017. PMID: 28318986 Free article. No abstract available.
514 results