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Mutational analysis of COQ2 in patients with MSA in Italy.
Ronchi D, Di Biase E, Franco G, Melzi V, Del Sorbo F, Elia A, Barzaghi C, Garavaglia B, Bergamini C, Fato R, Mora G, Del Bo R, Fortunato F, Borellini L, Trezzi I, Compagnoni GM, Monfrini E, Frattini E, Bonato S, Cogiamanian F, Ardolino G, Priori A, Bresolin N, Corti S, Comi GP, Di Fonzo A. Ronchi D, et al. Among authors: bonato s. Neurobiol Aging. 2016 Sep;45:213.e1-213.e2. doi: 10.1016/j.neurobiolaging.2016.05.022. Epub 2016 Jun 7. Neurobiol Aging. 2016. PMID: 27394078
Neurofascin (NFASC) gene mutation causes autosomal recessive ataxia with demyelinating neuropathy.
Monfrini E, Straniero L, Bonato S, Monzio Compagnoni G, Bordoni A, Dilena R, Rinchetti P, Silipigni R, Ronchi D, Corti S, Comi GP, Bresolin N, Duga S, Di Fonzo A. Monfrini E, et al. Among authors: bonato s. Parkinsonism Relat Disord. 2019 Jun;63:66-72. doi: 10.1016/j.parkreldis.2019.02.045. Epub 2019 Mar 1. Parkinsonism Relat Disord. 2019. PMID: 30850329 Free article.
Dystonia-ataxia syndrome with permanent torsional nystagmus caused by ECHS1 deficiency.
Ronchi D, Monfrini E, Bonato S, Mancinelli V, Cinnante C, Salani S, Bordoni A, Ciscato P, Fortunato F, Villa M, Di Fonzo A, Corti S, Bresolin N, Comi GP. Ronchi D, et al. Among authors: bonato s. Ann Clin Transl Neurol. 2020 May;7(5):839-845. doi: 10.1002/acn3.51025. Epub 2020 Apr 24. Ann Clin Transl Neurol. 2020. PMID: 32329585 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: bonato s. 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.
90 results