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1978 1
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1999 2
2000 2
2001 3
2002 5
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2007 2
2008 3
2009 6
2010 3
2011 6
2012 9
2013 7
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234 results

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Page 1
Did you mean gatti a[AUTHOR] (607 results)?
Deep Phenotyping of F64L Mutation in a Multicentric Cohort of Patisiran-Treated Hereditary Transthyretin Amyloidosis Patients (Patisiranitaly).
Ceccanti M, Guaraldi P, Romano A, Antonini G, Barilaro A, Briani C, Burattini M, Gianoli M, Carlini G, Cianci V, Dossi MC, Di Lisi D, Di Muzio A, Ratti A, Filosto M, Gasverde S, Gemelli C, Gentile L, Goglia M, Leonardi L, Longhi S, Lotti A, Manganelli F, Mazzeo A, Augello SM, Milella G, Novo G, Pareyson D, Fenu S, Palumbo G, Petrelli C, Poli L, Pradotto LG, Russo M, Salvalaggio A, Sciarrone MA, Sellitti L, Tagliapietra M, Tozza S, Castiglia M, Turri M, Verriello L, Chimenti C, Vitali F, Brighina F, Rini N, Inghilleri M, D'Angelo R, Abelardo D, Cambieri C, Libonati L, Moret F, Luigetti M, Di Stefano V. Ceccanti M, et al. Among authors: ratti a. Eur J Neurol. 2026 Jun;33(6):e70657. doi: 10.1111/ene.70657. Eur J Neurol. 2026. PMID: 42226514 Free PMC article.
Functional validation of the novel KIF5A p.R17Q VUS reveals defective axonal transport in iPSC-motoneurons from a SPG10 patient.
Santangelo S, Casiraghi V, Fallini C, Invernizzi S, Peverelli S, Bertocchi M, Feole M, Cozzi M, Magri S, Poletti A, Bossolasco P, Taroni F, Silani V, Ratti A. Santangelo S, et al. Among authors: ratti a. Front Genet. 2026 Feb 27;17:1774170. doi: 10.3389/fgene.2026.1774170. eCollection 2026. Front Genet. 2026. PMID: 41836058 Free PMC article.
Phenotype-Genotype Correlations in Early-Onset Myelin Protein Zero-Related Neuropathies.
Laurini C, Danti FR, Russo M, Tozza S, Massucco S, Bertini A, Pisciotta C, D'Arma F, Gentile L, Falzone YM, Ratti A, Catteruccia M, Fiorillo C, Cicala G, Luigetti M, Magri S, Bellone E, Fabrizi GM, Manganelli F, Grandis M, Mazzeo A, Pareyson D, Moroni I, Previtali SC. Laurini C, et al. Among authors: ratti a. Neurol Genet. 2025 Oct 10;11(6):e200314. doi: 10.1212/NXG.0000000000200314. eCollection 2025 Dec. Neurol Genet. 2025. PMID: 41127313 Free PMC article.
MYC-driven gliosis impairs neuron-glia communication in amyotrophic lateral sclerosis.
Fioretti PV, Barbieri A, Migazzi A, Bressan D, Grassano M, Donini L, Roccuzzo M, Torrieri MC, Conci F, Ferracci E, Invernizzi S, Bowden KM, Bacchetti F, Cappelli S, Peroni D, Belli R, Pancher M, Mugoni V, Scarduelli G, Gianesello M, Pasetto L, Canarutto G, Carra S, Soldano A, Bisio A, Robbiati S, Valentini C, Nardella C, Piazza S, D'Agostino VG, Quattrone A, Sleiman S, Whitfield JR, Soucek L, Vignoli B, Viero G, Tiberi L, Zippo A, Demichelis F, Bonetto V, Milanese M, Buratti E, Verde F, Ticozzi N, Calvo A, Ratti A, Shaw PJ, Terenzio M, Chiacchiera F, Pennuto M, Basso M. Fioretti PV, et al. Among authors: ratti a. Brain. 2026 May 5;149(5):1604-1622. doi: 10.1093/brain/awaf360. Brain. 2026. PMID: 41004427 Free PMC article.
Whole genome sequencing analysis in primary lateral sclerosis (PLS) patients reveals mutations in neurological diseases-causing genes.
Manini A, Brusati A, Grassano M, Scacciatella G, Peverelli S, Spagliardi J, Pensato V, Doretti A, Vasta R, Manera U, Canosa A, Brunetti M, Gentilini D, Messina S, Verde F, Moglia C, Morelli C, Dalla Bella E, Keagle PJ, Landers JE, Gellera C, Lauria Pinter G, Chiò A, Ratti A, Calvo A, Silani V, Ticozzi N. Manini A, et al. Among authors: ratti a. J Neurol. 2025 Aug 22;272(9):587. doi: 10.1007/s00415-025-13328-1. J Neurol. 2025. PMID: 40844737
Prevalence of hereditary transthyretin amyloidosis in CIDP patients with red flags: a multicenter genetic screening and misdiagnosis analysis.
Doneddu PE, Moretti G, Di Stefano V, Falzone Y, Leonardi L, Luigetti M, Mataluni G, Gentile L, Carpo M, Barilaro A, Filosto M, Vegezzi E, Inghilleri M, Canale F, Brighina F, Matà S, Ratti A, Forcina F, Siconolfi G, Lozi C, Mazzeo A, Mollo U, Risi B, Cosentino G, Moret F, Fasano C, Todisco V, Russo M, Nobile-Orazio E. Doneddu PE, et al. Among authors: ratti a. J Neurol. 2025 Jul 16;272(8):515. doi: 10.1007/s00415-025-13218-6. J Neurol. 2025. PMID: 40670759
234 results