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Expanding the clinical-pathological and genetic spectrum of RYR1-related congenital myopathies with cores and minicores: an Italian population study.
Fusto A, Cassandrini D, Fiorillo C, Codemo V, Astrea G, D'Amico A, Maggi L, Magri F, Pane M, Tasca G, Sabbatini D, Bello L, Battini R, Bernasconi P, Fattori F, Bertini ES, Comi G, Messina S, Mongini T, Moroni I, Panicucci C, Berardinelli A, Donati A, Nigro V, Pini A, Giannotta M, Dosi C, Ricci E, Mercuri E, Minervini G, Tosatto S, Santorelli F, Bruno C, Pegoraro E. Fusto A, et al. Among authors: codemo v. Acta Neuropathol Commun. 2022 Apr 15;10(1):54. doi: 10.1186/s40478-022-01357-0. Acta Neuropathol Commun. 2022. PMID: 35428369 Free PMC article.
Centronuclear myopathy related to dynamin 2 mutations: clinical, morphological, muscle imaging and genetic features of an Italian cohort.
Catteruccia M, Fattori F, Codemo V, Ruggiero L, Maggi L, Tasca G, Fiorillo C, Pane M, Berardinelli A, Verardo M, Bragato C, Mora M, Morandi L, Bruno C, Santoro L, Pegoraro E, Mercuri E, Bertini E, D'Amico A. Catteruccia M, et al. Among authors: codemo v. Neuromuscul Disord. 2013 Mar;23(3):229-38. doi: 10.1016/j.nmd.2012.12.009. Epub 2013 Feb 8. Neuromuscul Disord. 2013. PMID: 23394783 Free PMC article.
Centronuclear myopathies: genotype-phenotype correlation and frequency of defined genetic forms in an Italian cohort.
Fattori F, Maggi L, Bruno C, Cassandrini D, Codemo V, Catteruccia M, Tasca G, Berardinelli A, Magri F, Pane M, Rubegni A, Santoro L, Ruggiero L, Fiorini P, Pini A, Mongini T, Messina S, Brisca G, Colombo I, Astrea G, Fiorillo C, Bragato C, Moroni I, Pegoraro E, D'Apice MR, Alfei E, Mora M, Morandi L, Donati A, Evilä A, Vihola A, Udd B, Bernansconi P, Mercuri E, Santorelli FM, Bertini E, D'Amico A. Fattori F, et al. Among authors: codemo v. J Neurol. 2015 Jul;262(7):1728-40. doi: 10.1007/s00415-015-7757-9. Epub 2015 May 10. J Neurol. 2015. PMID: 25957634
SERCA1 protein expression in muscle of patients with Brody disease and Brody syndrome and in cultured human muscle fibers.
Guglielmi V, Vattemi G, Gualandi F, Voermans NC, Marini M, Scotton C, Pegoraro E, Oosterhof A, Kósa M, Zádor E, Valente EM, De Grandis D, Neri M, Codemo V, Novelli A, van Kuppevelt TH, Dallapiccola B, van Engelen BG, Ferlini A, Tomelleri G. Guglielmi V, et al. Among authors: codemo v. Mol Genet Metab. 2013 Sep-Oct;110(1-2):162-9. doi: 10.1016/j.ymgme.2013.07.015. Epub 2013 Jul 20. Mol Genet Metab. 2013. PMID: 23911890
Correction to: Current territorial organization for access to revascularization therapies for acute ischemic stroke in the Veneto region (Italy) from 2017 to 2021.
Cappellari M, Bonetti B, Baracchini C, Corbetta M, De Boni A, Critelli A, Tonello S, Codemo V, Marcon M, Turinese E, Bombardi R, Basile AM, Ruzza G, Cadaldini M, Mampreso E, Marsala SZ, Padoan R, Marini B, Gaudenzi A, Tonon A, Masato M, Baldi A, Turazzini M, Zanette G, Adami A, Saia M, Bovi P. Cappellari M, et al. Among authors: codemo v. Neurol Sci. 2023 Oct;44(10):3769. doi: 10.1007/s10072-023-06890-x. Neurol Sci. 2023. PMID: 37294391 No abstract available.
Current territorial organization for access to revascularization therapies for acute ischemic stroke in the Veneto region (Italy) from 2017 to 2021.
Cappellari M, Bonetti B, Baracchini C, Corbetta M, De Boni A, Critelli A, Tonello S, Codemo V, Marcon M, Turinese E, Bombardi R, Basile AM, Ruzza G, Cadaldini M, Mampreso E, Marsala SZ, Padoan R, Marini B, Gaudenzi A, Tonon A, Masato M, Baldi A, Turazzini M, Zanette G, Adami A, Saia M, Bovi P. Cappellari M, et al. Among authors: codemo v. Neurol Sci. 2023 Jun;44(6):2033-2039. doi: 10.1007/s10072-023-06662-7. Epub 2023 Feb 8. Neurol Sci. 2023. PMID: 36753010 Free PMC article.
Neurological complications in hyperemesis gravidarum.
Zara G, Codemo V, Palmieri A, Schiff S, Cagnin A, Citton V, Manara R. Zara G, et al. Among authors: codemo v. Neurol Sci. 2012 Feb;33(1):133-5. doi: 10.1007/s10072-011-0660-y. Epub 2011 Jul 1. Neurol Sci. 2012. PMID: 21720901