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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2004 1
2008 1
2010 1
2011 1
2012 4
2013 2
2014 1
2015 3
2016 2
2017 3
2018 5
2019 3
2020 7
2021 5
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33 results
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Page 1
Complement Inhibition for the Treatment of Myasthenia Gravis.
Mantegazza R, Vanoli F, Frangiamore R, Cavalcante P. Mantegazza R, et al. Among authors: vanoli f. Immunotargets Ther. 2020 Dec 15;9:317-331. doi: 10.2147/ITT.S261414. eCollection 2020. Immunotargets Ther. 2020. PMID: 33365280 Free PMC article. Review.
Muscle involvement in myasthenia gravis: Expanding the clinical spectrum of Myasthenia-Myositis association from a large cohort of patients.
Garibaldi M, Fionda L, Vanoli F, Leonardi L, Loreti S, Bucci E, Di Pasquale A, Morino S, Vizzaccaro E, Merlonghi G, Ceccanti M, Lucchini M, Mirabella M, Andreetta F, Pennisi EM, Petrucci A, Salvetti M, Antonini G. Garibaldi M, et al. Among authors: vanoli f. Autoimmun Rev. 2020 Apr;19(4):102498. doi: 10.1016/j.autrev.2020.102498. Epub 2020 Feb 14. Autoimmun Rev. 2020. PMID: 32062029 Review.
Nerve high-resolution ultrasonography in tangier disease.
Pasquale AD, Leonardi L, Fionda L, Vanoli F, Garibaldi M, Inghilleri M, Ceccanti M, Cambieri C, Onesti E, Antonini G. Pasquale AD, et al. Among authors: vanoli f. Muscle Nerve. 2019 May;59(5):587-590. doi: 10.1002/mus.26427. Epub 2019 Feb 7. Muscle Nerve. 2019. PMID: 30680752
miRNA in spinal muscular atrophy pathogenesis and therapy.
Magri F, Vanoli F, Corti S. Magri F, et al. Among authors: vanoli f. J Cell Mol Med. 2018 Feb;22(2):755-767. doi: 10.1111/jcmm.13450. Epub 2017 Nov 21. J Cell Mol Med. 2018. PMID: 29160009 Free PMC article. Review.
ATTRv amyloidosis Italian Registry: clinical and epidemiological data.
Russo M, Obici L, Bartolomei I, Cappelli F, Luigetti M, Fenu S, Cavallaro T, Chiappini MG, Gemelli C, Pradotto LG, Manganelli F, Leonardi L, My F, Sampaolo S, Briani C, Gentile L, Stancanelli C, Di Buduo E, Pacciolla P, Salvi F, Casagrande S, Bisogni G, Calabrese D, Vanoli F, Di Iorio G, Antonini G, Santoro L, Mauro A, Grandis M, Di Girolamo M, Fabrizi GM, Pareyson D, Sabatelli M, Perfetto F, Rapezzi C, Merlini G, Mazzeo A, Vita G. Russo M, et al. Among authors: vanoli f. Amyloid. 2020 Dec;27(4):259-265. doi: 10.1080/13506129.2020.1794807. Epub 2020 Jul 22. Amyloid. 2020. PMID: 32696671
Gender effect on cardiac involvement in myotonic dystrophy type 1.
Garibaldi M, Lauletta A, Bucci E, Fionda L, Vanoli F, Leonardi L, Alfieri G, Tufano L, Morino S, Merlonghi G, Anibaldi P, Salvetti M, Testa M, Antonini G. Garibaldi M, et al. Among authors: vanoli f. Eur J Neurol. 2021 Apr;28(4):1366-1374. doi: 10.1111/ene.14665. Epub 2020 Dec 25. Eur J Neurol. 2021. PMID: 33283405
Novel ACTA1 mutation causes late-presenting nemaline myopathy with unusual dark cores.
Garibaldi M, Fattori F, Pennisi EM, Merlonghi G, Fionda L, Vanoli F, Leonardi L, Bucci E, Morino S, Micaloni A, Tartaglione T, Uijterwijk B, Zierikzee M, Ottenheijm C, Bertini ES, Stoppacciaro A, Raffa S, Salvetti M, Antonini G. Garibaldi M, et al. Among authors: vanoli f. Neuromuscul Disord. 2021 Feb;31(2):139-148. doi: 10.1016/j.nmd.2020.11.012. Epub 2020 Nov 30. Neuromuscul Disord. 2021. PMID: 33384202
Nerve ultrasonography findings as possible pitfall in differential diagnosis between hereditary transthyretin amyloidosis with polyneuropathy and chronic inflammatory demyelinating polyneuropathy.
Leonardi L, Vanoli F, Fionda L, Loreti S, Garibaldi M, Morino S, Salvetti M, Russo D, Musumeci B, Antonini G. Leonardi L, et al. Among authors: vanoli f. Neurol Sci. 2020 Dec;41(12):3775-3778. doi: 10.1007/s10072-020-04717-7. Epub 2020 Sep 16. Neurol Sci. 2020. PMID: 32936357
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