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SCN4A as modifier gene in patients with myotonic dystrophy type 2.
Binda A, Renna LV, Bosè F, Brigonzi E, Botta A, Valaperta R, Fossati B, Rivolta I, Meola G, Cardani R. Binda A, et al. Among authors: fossati b. Sci Rep. 2018 Jul 23;8(1):11058. doi: 10.1038/s41598-018-29302-z. Sci Rep. 2018. PMID: 30038349 Free PMC article.
Validation of plasma microRNAs as biomarkers for myotonic dystrophy type 1.
Perfetti A, Greco S, Cardani R, Fossati B, Cuomo G, Valaperta R, Ambrogi F, Cortese A, Botta A, Mignarri A, Santoro M, Gaetano C, Costa E, Dotti MT, Silvestri G, Massa R, Meola G, Martelli F. Perfetti A, et al. Among authors: fossati b. Sci Rep. 2016 Dec 1;6:38174. doi: 10.1038/srep38174. Sci Rep. 2016. PMID: 27905532 Free PMC article. Clinical Trial.
High-sensitive cardiac troponin T (hs-cTnT) assay as serum biomarker to predict cardiac risk in myotonic dystrophy: A case-control study.
Valaperta R, Gaeta M, Cardani R, Lombardi F, Rampoldi B, De Siena C, Mori F, Fossati B, Gaia P, Ferraro OE, Villani S, Iachettini S, Piccoli M, Cirillo F, Pusineri E, Meola G, Costa E. Valaperta R, et al. Among authors: fossati b. Clin Chim Acta. 2016 Dec 1;463:122-128. doi: 10.1016/j.cca.2016.10.026. Epub 2016 Oct 22. Clin Chim Acta. 2016. PMID: 27780717
Flecainide-Induced Brugada Syndrome in a Patient With Skeletal Muscle Sodium Channelopathy: A Case Report With Critical Therapeutical Implications and Review of the Literature.
Cavalli M, Fossati B, Vitale R, Brigonzi E, Ricigliano VAG, Saraceno L, Cardani R, Pappone C, Meola G. Cavalli M, et al. Among authors: fossati b. Front Neurol. 2018 May 30;9:385. doi: 10.3389/fneur.2018.00385. eCollection 2018. Front Neurol. 2018. PMID: 29899727 Free PMC article.
68 results