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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
A 34-year longitudinal study on long-term cardiac outcomes in DM1 patients with normal ECG at baseline at an Italian clinical centre.
Bucci E, Testa M, Licchelli L, Frattari A, El Halabieh NA, Gabriele E, Pignatelli G, De Santis T, Fionda L, Vanoli F, Morino S, Garibaldi M, Di Pasquale A, Vanacore N, Botta A, Antonini G. Bucci E, et al. Among authors: vanoli f. J Neurol. 2018 Apr;265(4):885-895. doi: 10.1007/s00415-018-8773-3. Epub 2018 Feb 10. J Neurol. 2018. PMID: 29429070
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.
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
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
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
59 results