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2010 1
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Page 1
Editorial: Tubulinopathies: fundamental and clinical challenges.
Sferra A, Bertini E, Haase G. Sferra A, et al. Front Cell Neurosci. 2023 Oct 13;17:1296958. doi: 10.3389/fncel.2023.1296958. eCollection 2023. Front Cell Neurosci. 2023. PMID: 37927444 Free PMC article. No abstract available.
The cytoskeletal arrangements necessary to neurogenesis.
Compagnucci C, Piemonte F, Sferra A, Piermarini E, Bertini E. Compagnucci C, et al. Among authors: sferra a. Oncotarget. 2016 Apr 12;7(15):19414-29. doi: 10.18632/oncotarget.6838. Oncotarget. 2016. PMID: 26760504 Free PMC article. Review.
Heterozygous KIF1A variants underlie a wide spectrum of neurodevelopmental and neurodegenerative disorders.
Nicita F, Ginevrino M, Travaglini L, D'Arrigo S, Zorzi G, Borgatti R, Terrone G, Catteruccia M, Vasco G, Brankovic V, Siliquini S, Romano S, Veredice C, Pedemonte M, Armando M, Lettori D, Stregapede F, Bosco L, Sferra A, Tessarollo V, Romaniello R, Ristori G, Bertini E, Valente EM, Zanni G. Nicita F, et al. Among authors: sferra a. J Med Genet. 2021 Jul;58(7):475-483. doi: 10.1136/jmedgenet-2020-107007. Epub 2020 Jul 31. J Med Genet. 2021. PMID: 32737135
Biallelic mutations in RNF220 cause laminopathies featuring leukodystrophy, ataxia and deafness.
Sferra A, Fortugno P, Motta M, Aiello C, Petrini S, Ciolfi A, Cipressa F, Moroni I, Leuzzi V, Pieroni L, Marini F, Boespflug Tanguy O, Eymard-Pierre E, Danti FR, Compagnucci C, Zambruno G, Brusco A, Santorelli FM, Chiapparini L, Francalanci P, Loizzo AL, Tartaglia M, Cestra G, Bertini E. Sferra A, et al. Brain. 2021 Nov 29;144(10):3020-3035. doi: 10.1093/brain/awab185. Brain. 2021. PMID: 33964137 Free article.
18 results