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Expanding the spectrum of neonatal-onset AIFM1-associated disorders.
Zambon AA, Ghezzi D, Baldoli C, Cutillo G, Fontana K, Sofia V, Patricelli MG, Nasca A, Vinci S, Spiga I, Lamantea E, Fanelli GF, Sora MGN, Rovelli R, Poloniato A, Carrera P, Filippi M, Barera G. Zambon AA, et al. Among authors: filippi m. Ann Clin Transl Neurol. 2023 Oct;10(10):1844-1853. doi: 10.1002/acn3.51876. Epub 2023 Aug 29. Ann Clin Transl Neurol. 2023. PMID: 37644805 Free PMC article.
Structural and functional brain signatures of C9orf72 in motor neuron disease.
Agosta F, Ferraro PM, Riva N, Spinelli EG, Domi T, Carrera P, Copetti M, Falzone Y, Ferrari M, Lunetta C, Comi G, Falini A, Quattrini A, Filippi M. Agosta F, et al. Among authors: filippi m. Neurobiol Aging. 2017 Sep;57:206-219. doi: 10.1016/j.neurobiolaging.2017.05.024. Epub 2017 Jun 6. Neurobiol Aging. 2017. PMID: 28666709
Brain and cord imaging features in neuromyelitis optica spectrum disorders.
Cacciaguerra L, Meani A, Mesaros S, Radaelli M, Palace J, Dujmovic-Basuroski I, Pagani E, Martinelli V, Matthews L, Drulovic J, Leite MI, Comi G, Filippi M, Rocca MA. Cacciaguerra L, et al. Among authors: filippi m. Ann Neurol. 2019 Mar;85(3):371-384. doi: 10.1002/ana.25411. Epub 2019 Jan 28. Ann Neurol. 2019. PMID: 30635936
Survival prediction models in motor neuron disease.
Agosta F, Spinelli EG, Riva N, Fontana A, Basaia S, Canu E, Castelnovo V, Falzone Y, Carrera P, Comi G, Filippi M. Agosta F, et al. Among authors: filippi m. Eur J Neurol. 2019 Sep;26(9):1143-1152. doi: 10.1111/ene.13957. Epub 2019 Apr 20. Eur J Neurol. 2019. PMID: 30920076
Concurrence of NMOSD and ALS in a patient with hexanucleotide repeat expansions of C9orf72.
Falzone YM, Radaelli M, Agosta F, Domi T, Guerrieri S, Spinelli EG, Pozzi L, Carrera P, Ferrari M, Comi G, Filippi M, Quattrini A, Riva N. Falzone YM, et al. Among authors: filippi m. Amyotroph Lateral Scler Frontotemporal Degener. 2019 Aug;20(5-6):449-452. doi: 10.1080/21678421.2019.1604761. Epub 2019 Apr 22. Amyotroph Lateral Scler Frontotemporal Degener. 2019. PMID: 31007077
Serum phosphorylated neurofilament heavy-chain levels reflect phenotypic heterogeneity and are an independent predictor of survival in motor neuron disease.
Falzone YM, Domi T, Agosta F, Pozzi L, Schito P, Fazio R, Del Carro U, Barbieri A, Comola M, Leocani L, Comi G, Carrera P, Filippi M, Quattrini A, Riva N. Falzone YM, et al. Among authors: filippi m. J Neurol. 2020 Aug;267(8):2272-2280. doi: 10.1007/s00415-020-09838-9. Epub 2020 Apr 18. J Neurol. 2020. PMID: 32306171 Free PMC article.
Burden of Rare Variants in ALS and Axonal Hereditary Neuropathy Genes Influence Survival in ALS: Insights from a Next Generation Sequencing Study of an Italian ALS Cohort.
Scarlino S, Domi T, Pozzi L, Romano A, Pipitone GB, Falzone YM, Mosca L, Penco S, Lunetta C, Sansone V, Tremolizzo L, Fazio R, Agosta F, Filippi M, Carrera P, Riva N, Quattrini A. Scarlino S, et al. Among authors: filippi m. Int J Mol Sci. 2020 May 8;21(9):3346. doi: 10.3390/ijms21093346. Int J Mol Sci. 2020. PMID: 32397312 Free PMC article.
Refractory anti-NMDAR encephalitis successfully treated with bortezomib and associated movements disorders controlled with tramadol: a case report with literature review.
Lazzarin SM, Vabanesi M, Cecchetti G, Fazio R, Fanelli GF, Volonté MA, Genchi A, Giordano A, Martinelli V, Colombo S, Beccaria P, Mucci M, Peccatori J, Filippi M, Minicucci F. Lazzarin SM, et al. Among authors: filippi m. J Neurol. 2020 Aug;267(8):2462-2468. doi: 10.1007/s00415-020-09988-w. Epub 2020 Jun 13. J Neurol. 2020. PMID: 32535682 Review.
1,957 results