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A Novel Mutation of GFAP Causing Adult-Onset Alexander Disease.
Ciammola A, Sangalli D, Sassone J, Poletti B, Carelli L, Banfi P, Pappacoda G, Ceccherini I, Grossi A, Maderna L, Pingue M, Girotti F, Silani V. Ciammola A, et al. Among authors: girotti f. Front Neurol. 2019 Nov 6;10:1124. doi: 10.3389/fneur.2019.01124. eCollection 2019. Front Neurol. 2019. PMID: 31781017 Free PMC article.
Parkinsonian Syndromes in Motor Neuron Disease: A Clinical Study.
Pasquini J, Trogu F, Morelli C, Poletti B, Girotti F, Peverelli S, Brusati A, Ratti A, Ciammola A, Silani V, Ticozzi N. Pasquini J, et al. Among authors: girotti f. Front Aging Neurosci. 2022 Jun 27;14:917706. doi: 10.3389/fnagi.2022.917706. eCollection 2022. Front Aging Neurosci. 2022. PMID: 35832068 Free PMC article.
X-linked Parkinsonism with Intellectual Disability caused by novel mutations and somatic mosaicism in RAB39B gene.
Ciammola A, Carrera P, Di Fonzo A, Sassone J, Villa R, Poletti B, Ferrari M, Girotti F, Monfrini E, Buongarzone G, Silani V, Cinnante CM, Mignogna ML, D'Adamo P, Bonati MT. Ciammola A, et al. Among authors: girotti f. Parkinsonism Relat Disord. 2017 Nov;44:142-146. doi: 10.1016/j.parkreldis.2017.08.021. Epub 2017 Aug 26. Parkinsonism Relat Disord. 2017. PMID: 28851564
Association of Clinically Evident Eye Movement Abnormalities With Motor and Cognitive Features in Patients With Motor Neuron Disorders.
Poletti B, Solca F, Carelli L, Diena A, Colombo E, Torre S, Maranzano A, Greco L, Cozza F, Lizio A, Ferrucci R, Girotti F, Verde F, Morelli C, Lunetta C, Silani V, Ticozzi N. Poletti B, et al. Among authors: girotti f. Neurology. 2021 Nov 2;97(18):e1835-e1846. doi: 10.1212/WNL.0000000000012774. Epub 2021 Sep 9. Neurology. 2021. PMID: 34504031 Free PMC article.
144 results