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Correction: Olfactory swab sampling optimization for α-synuclein aggregate detection in patients with Parkinson's disease.
Bongianni M, Catalan M, Perra D, Fontana E, Janes F, Bertolotti C, Sacchetto L, Capaldi S, Tagliapietra M, Polverino P, Tommasini V, Bellavita G, Kachoie EA, Baruca R, Bernardini A, Valente M, Fiorini M, Bronzato E, Tamburin S, Bertolasi L, Brozzetti L, Cecchini MP, Gigli G, Monaco S, Manganotti P, Zanusso G. Bongianni M, et al. Among authors: fontana e. Transl Neurodegener. 2022 Aug 12;11(1):38. doi: 10.1186/s40035-022-00312-2. Transl Neurodegener. 2022. PMID: 35962443 Free PMC article. No abstract available.
Olfactory swab sampling optimization for α-synuclein aggregate detection in patients with Parkinson's disease.
Bongianni M, Catalan M, Perra D, Fontana E, Janes F, Bertolotti C, Sacchetto L, Capaldi S, Tagliapietra M, Polverino P, Tommasini V, Bellavita G, Kachoie EA, Baruca R, Bernardini A, Valente M, Fiorini M, Bronzato E, Tamburin S, Bertolasi L, Brozzetti L, Cecchini MP, Gigli G, Monaco S, Manganotti P, Zanusso G. Bongianni M, et al. Among authors: fontana e. Transl Neurodegener. 2022 Jul 28;11(1):37. doi: 10.1186/s40035-022-00311-3. Transl Neurodegener. 2022. PMID: 35902902 Free PMC article.
Adaptive behaviour in adolescents and adults with Dravet syndrome.
Lo Barco T, Offredi F, Castino E, Proietti J, Cossu A, Fiorini E, Fontana E, Cantalupo G, Dalla Bernardina B, Darra F. Lo Barco T, et al. Among authors: fontana e. Dev Med Child Neurol. 2023 Jun;65(6):838-846. doi: 10.1111/dmcn.15448. Epub 2022 Oct 31. Dev Med Child Neurol. 2023. PMID: 36316303
Myoclonic status in nonprogressive encephalopathies.
Dalla Bernardina B, Fontana E, Darra F. Dalla Bernardina B, et al. Among authors: fontana e. Adv Neurol. 2005;95:59-70. Adv Neurol. 2005. PMID: 15508914 Review. No abstract available.
Progressive myoclonic encephalopathy in X-linked hypogamma-globulinemia. Case report, review of the literature and its relationship with progressive encephalopathy in children with A.I.D.S.
Colamaria V, Marradi P, Boner A, Pajno-Ferrara F, Procacci C, Cesaro G, La Selva L, Capovilla G, Fontana E, Dalla Bernardina B. Colamaria V, et al. Among authors: fontana e. Neuropediatrics. 1989 Nov;20(4):223-9. doi: 10.1055/s-2008-1071298. Neuropediatrics. 1989. PMID: 2514400 Review.
No evidence of GABRG2 mutations in severe myoclonic epilepsy of infancy.
Madia F, Gennaro E, Cecconi M, Buti D, Capovilla G, Dalla Bernardina B, Elia M, Ferrari A, Fontana E, Gaggero R, Giannotta M, Giordano L, Granata T, La Selva L, Luisa Lispi M, Santucci M, Vanadia F, Veggiotti P, Vigliano P, Viri M, Dagna Bricarelli F, Bianchi A, Zara F. Madia F, et al. Among authors: fontana e. Epilepsy Res. 2003 Mar;53(3):196-200. doi: 10.1016/s0920-1211(03)00022-6. Epilepsy Res. 2003. PMID: 12694927
324 results