Zobrazeno 1 - 10
of 77
pro vyhledávání: '"Federica Dagradi"'
In a case of female-to-male sex reassignment, testosterone therapy switches on an underlying Brugada
Publikováno v:
International Journal of Arrhythmia, Vol 21, Iss 1, Pp 1-4 (2020)
Abstract Background The Brugada syndrome, diagnosed by a typical electrocardiographic pattern, is a genetic condition characterised by an increased risk of potentially lethal ventricular arrhythmias and sudden cardiac death. Even if its pathophysiolo
Externí odkaz:
https://doaj.org/article/4454bdb5e22e4b34bdad86521fe1a5a8
Autor:
Manuela Mura, Yee-ki Lee, Monia Ginevrino, Rita Zappatore, Federica Pisano, Marina Boni, Federica Dagradi, Lia Crotti, Enza Maria Valente, Peter J. Schwartz, Hung-Fat Tse, Massimiliano Gnecchi
Publikováno v:
Stem Cell Research, Vol 29, Iss , Pp 157-161 (2018)
We report the generation of human induced pluripotent stem cells (hiPSCs) from dermal fibroblasts of a female patient carrier of the two compound heterozygous mutations c.568 C>T p.R190W (maternal allele), and c.1781 G>A p.R594Q (paternal allele) on
Externí odkaz:
https://doaj.org/article/631c74e9873341e2884a30e0b0f5f660
Autor:
Cuilan Li, Lia Crotti, Veronica Dusi, Federica Dagradi, Gaetano M. De Ferrari, Roberto Rordorf, Maria Shkolnikova, Peter J. Schwartz, Carla Spazzolini, Attilio Odero, Luigi Pugliese, Silvia Castelletti, Alessandro Vicentini
Publikováno v:
JACC: Clinical Electrophysiology. 8:281-294
Objectives This study sought to report our single-center experience with left cardiac sympathetic denervation (LCSD) for long QT syndrome (LQTS) since 1973. Background LCSD is still underutilized because clinicians are often uncertain whether to use
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5f7285c26478fdc075270232d4bfb365
https://doi.org/10.1016/j.jacep.2021.09.002
https://doi.org/10.1016/j.jacep.2021.09.002
Autor:
Carla Spazzolini, Isabelle Denjoy, Roel L.H.M.G. Spätjens, Peter J. Schwartz, Maria Christina Kotta, Paul A. Brink, Cristina Moreno, Kristina H. Haugaa, Sandrine R.M. Seyen, Maria Shkolnikova, Federica Dagradi, Lia Crotti, Marshall Heradien, Paul G.A. Volders, Silvia Castelletti, Matteo Pedrazzini
Publikováno v:
Eur Heart J
European Heart Journal, 42(46), 4743-4755. Oxford University Press
European Heart Journal, 42(46), 4743-4755. Oxford University Press
Aims Mutation type, location, dominant-negative I Ks reduction, and possibly loss of cyclic adenosine monophosphate (cAMP)-dependent I Ks stimulation via protein kinase A (PKA) influence the clinical severity of long QT syndrome type 1 (LQT1). Given
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::844d33f416c443ba9630554a3eb61ac2
https://doi.org/10.1093/eurheartj/ehab582
https://doi.org/10.1093/eurheartj/ehab582
Autor:
Roberto Menè, Federica Dagradi, Fulvio Giovenzana, Francesco Maria Brasca, Giulia Girardengo, Gianfranco Parati, Giovanni Battista Perego, Lia Crotti, Peter J Schwartz
Publikováno v:
European Heart Journal Supplements. 24
Brugada Syndrome (BrS) is one of the most common channelopathies and is related to an increased risk of ventricular arrhythmias. Current guidelines recommend the implantation of a Cardiac Defibrillator (ICD) in those patients that have a diagnostic E
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::554f25d4290adeeee2cb5ff35ce76848
https://doi.org/10.1093/eurheartjsupp/suac121.056
https://doi.org/10.1093/eurheartjsupp/suac121.056
Autor:
Dan Ye, Todd J. Herron, Ryan P. O'Connell, Michael J. Ackerman, Silvia Castelletti, Maria Christina Kotta, Charles Antzelevitch, Lia Crotti, Guadalupe Guerrero-Serna, Andre Monteiro da Rocha, Margherita Torchio, Hassan Hussein Musa, Justus M.B. Anumonwo, Michael A. Makara, Peter J. Mohler, Brad Rosinski, Cherisse A. Marcou, Vladislav V. Nesterenko, Michelle L. Milstein, David J. Tester, Federica Dagradi, Peter J. Schwartz
Publikováno v:
Am J Physiol Heart Circ Physiol
Synapse-associated protein 97 (SAP97) is a scaffolding protein crucial for the functional expression of several cardiac ion channels and therefore proper cardiac excitability. Alterations in the functional expression of SAP97 can modify the ionic cur
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bc7367f1cbcd25398921636223a2e5f2
https://doi.org/10.1152/ajpheart.00481.2019
https://doi.org/10.1152/ajpheart.00481.2019
Publikováno v:
Sport-related sudden cardiac death ISBN: 9783030804466
Sport-related sudden cardiac death
Sport-related sudden cardiac death
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d6aa3dcae32045f706504dd19784d9ef
https://doi.org/10.1007/978-3-030-80447-3_9
https://doi.org/10.1007/978-3-030-80447-3_9
Autor:
camilla torlasco, Franco Cecchi, P. J. Schwartz, G. Parati, L. Crotti, federica dagradi, Barbara Bilo, G. Perego, M. Revera, Anna Maria Di Blasio, Maria-Christina Kotta, Alice Ghidoni, Giulia Girardengo, Margherita Calcagnino
Publikováno v:
ScienceOpen Research (2015)
We present a case of arrhythmogenic cardiomyopathy with biventricular involvement and strong arrhythmic substrate, highlighting the need to consider more than a single diagnostic option when facing arrhythmic presentations in young patients and the g
Externí odkaz:
https://doaj.org/article/216f6347c3494809a1dcef6ff8927055
Autor:
Veronica Dusi, Luigi Pugliese, Gaetano M. De Ferrari, Attilio Odero, Lia Crotti, Federica Dagradi, Silvia Castelletti, Alessandro Vicentini, Roberto Rordorf, Cuilan Li, Maria Shkolnikova, Carla Spazzolini, Peter J. Schwartz
Publikováno v:
JACC. Clinical electrophysiology. 8(3)
Objectives:This study sought to report our single-center experience with left cardiac sympathetic denervation (LCSD) for long QT syndrome (LQTS) since 1973. Background:LCSD is still underutilized because clinicians are often uncertain whether to use
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::2ece37282c37fad300b025902127230a
https://pubmed.ncbi.nlm.nih.gov/35331423
https://pubmed.ncbi.nlm.nih.gov/35331423
Autor:
Krystian, Kozek, Yuko, Wada, Luca, Sala, Isabelle, Denjoy, Christian, Egly, Matthew J, O'Neill, Takeshi, Aiba, Wataru, Shimizu, Naomasa, Makita, Taisuke, Ishikawa, Lia, Crotti, Carla, Spazzolini, Maria-Christina, Kotta, Federica, Dagradi, Silvia, Castelletti, Matteo, Pedrazzini, Massimiliano, Gnecchi, Antoine, Leenhardt, Joe-Elie, Salem, Seiko, Ohno, Yi, Zuo, Andrew M, Glazer, Jonathan D, Mosley, Dan M, Roden, Bjorn C, Knollmann, Jeffrey D, Blume, Fabrice, Extramiana, Peter J, Schwartz, Minoru, Horie, Brett M, Kroncke
Publikováno v:
Circ Genom Precis Med
BACKGROUND -: The proliferation of genetic profiling has revealed many associations between genetic variations and disease. However, large-scale phenotyping efforts in largely healthy populations, coupled with DNA sequencing, suggest variants current
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f027932df3a42415a51e33c8d5e261f4
https://pubmed.ncbi.nlm.nih.gov/34309407
https://pubmed.ncbi.nlm.nih.gov/34309407