Zobrazeno 1 - 10
of 357
pro vyhledávání: '"CARLO NAPOLITANO"'
Autor:
Arthur A. M. Wilde, Christopher Semsarian, Manlio F. Márquez, Alireza Sepehri Shamloo, Michael J. Ackerman, Euan A. Ashley, Back Sternick Eduardo, Héctor Barajas‐Martinez, Elijah R. Behr, Connie R. Bezzina, Jeroen Breckpot, Philippe Charron, Priya Chockalingam, Lia Crotti, Michael H. Gollob, Steven Lubitz, Naomasa Makita, Seiko Ohno, Martín Ortiz‐Genga, Luciana Sacilotto, Eric Schulze‐Bahr, Wataru Shimizu, Nona Sotoodehnia, Rafik Tadros, James S. Ware, David S. Winlaw, Elizabeth S. Kaufman, Takeshi Aiba, Andreas Bollmann, Jong‐Il Choi, Aarti Dalal, Francisco Darrieux, John Giudicessi, Mariana Guerchicoff, Kui Hong, Andrew D. Krahn, Ciorsti Mac Intyre, Judith A. Mackall, Lluís Mont, Carlo Napolitano, Pablo Ochoa Juan, Petr Peichl, Alexandre C. Pereira, Peter J. Schwartz, Jon Skinner, Christoph Stellbrink, Jacob Tfelt‐Hansen, Thomas Deneke
Publikováno v:
Journal of Arrhythmia, Vol 38, Iss 4, Pp 491-553 (2022)
Externí odkaz:
https://doaj.org/article/065b869d10df4d35a27b0f57e20fcc2b
Autor:
Vittoria Di Mauro, Paola Ceriotti, Francesco Lodola, Nicolò Salvarani, Jessica Modica, Marie-Louise Bang, Andrea Mazzanti, Carlo Napolitano, Silvia G. Priori, Daniele Catalucci
Publikováno v:
Frontiers in Physiology, Vol 11 (2021)
Brugada syndrome (BrS) is an inherited arrhythmogenic disease that may lead to sudden cardiac death in young adults with structurally normal hearts. No pharmacological therapy is available for BrS patients. This situation highlights the urgent need t
Externí odkaz:
https://doaj.org/article/185089ae836f4f82a40fa10a9c2cfed3
Autor:
María Fernández-Velasco, Gema Ruiz-Hurtado, Angélica Rueda, Patricia Neco, Martha Mercado-Morales, Carmen Delgado, Carlo Napolitano, Silvia G Priori, Sylvain Richard, Ana María Gómez, Jean-Pierre Benitah
Publikováno v:
PLoS ONE, Vol 6, Iss 6, p e20863 (2011)
Ca(2+) mediates the functional coupling between L-type Ca(2+) channel (LTCC) and sarcoplasmic reticulum (SR) Ca(2+) release channel (ryanodine receptor, RyR), participating in key pathophysiological processes. This crosstalk manifests as the orthogra
Externí odkaz:
https://doaj.org/article/89d878fae0a748e4b4c3dfe1b3a0f3b9
Autor:
Michele Nicastro, Stephanie BONNAUD, Rafik Tadros, Philip Van Damme, Sean Jurgens, Pier Lambiase, Elijah Behr, Tomas Robyns, Julien Barc, Andrea Mazzanti, Manon BAUDIC, Sonia Van Dooren, Jean Baptiste Gourraud, Caroline Rooryck, Carlo Napolitano, Katja E Odening
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7a1e2b33f1d8a1693968971defce5031
https://doi.org/10.1038/s41588-022-01079-y
https://doi.org/10.1038/s41588-022-01079-y
Autor:
Andrea Mazzanti, Deni Kukavica, Alessandro Trancuccio, Mirella Memmi, Raffaella Bloise, Patrick Gambelli, Maira Marino, Martín Ortíz-Genga, Massimo Morini, Nicola Monteforte, Umberto Giordano, Roberto Keegan, Luca Tomasi, Aristides Anastasakis, Andrew M. Davis, Wataru Shimizu, Nico A. Blom, Demetrio Julián Santiago, Carlo Napolitano, Lorenzo Monserrat, Silvia G. Priori
Publikováno v:
JAMA Cardiol
JAMA cardiology, 7(5), 504-512. American Medical Association
JAMA Cardiology, 7(5), 504-512. AMER MEDICAL ASSOC
Mazzanti, A, Kukavica, D, Trancuccio, A, Memmi, M, Bloise, R, Gambelli, P, Marino, M, Ortíz-Genga, M, Morini, M, Monteforte, N, Giordano, U, Keegan, R, Tomasi, L, Anastasakis, A, Davis, A M, Shimizu, W, Blom, N A, Santiago, D J, Napolitano, C, Monserrat, L & Priori, S G 2022, ' Outcomes of Patients with Catecholaminergic Polymorphic Ventricular Tachycardia Treated with β-Blockers ', JAMA cardiology, vol. 7, no. 5, pp. 504-512 . https://doi.org/10.1001/jamacardio.2022.0219
JAMA cardiology, 7(5), 504-512. American Medical Association
JAMA Cardiology, 7(5), 504-512. AMER MEDICAL ASSOC
Mazzanti, A, Kukavica, D, Trancuccio, A, Memmi, M, Bloise, R, Gambelli, P, Marino, M, Ortíz-Genga, M, Morini, M, Monteforte, N, Giordano, U, Keegan, R, Tomasi, L, Anastasakis, A, Davis, A M, Shimizu, W, Blom, N A, Santiago, D J, Napolitano, C, Monserrat, L & Priori, S G 2022, ' Outcomes of Patients with Catecholaminergic Polymorphic Ventricular Tachycardia Treated with β-Blockers ', JAMA cardiology, vol. 7, no. 5, pp. 504-512 . https://doi.org/10.1001/jamacardio.2022.0219
Patients with catecholaminergic polymorphic ventricular tachycardia (CPVT) may experience life-threatening arrhythmic events (LTAEs) despite β-blocker treatment. Further complicating management, the role of implantable cardioverter defibrillator (IC
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c929e7cc08bf8cf5e5f9c580b72e5d54
https://europepmc.org/articles/PMC8968697/
https://europepmc.org/articles/PMC8968697/
Autor:
Alessandro Trancuccio, Andrea Mazzanti, Deni Kukavica, Carlo Arnò, Matteo Sturla, Maira Marino, Raffaela Bloise, Carlo Napolitano, Lorenzo Monti, Silvia G. Priori
Publikováno v:
European Heart Journal Supplements : Journal of the European Society of Cardiology
Aims Myocardial involvement has been reported in SARS-CoV-2 infection, especially in hospitalized patients during the acute phase of the disease. However, the exact prevalence and the clinical implications of cardiac involvement in young individuals
Autor:
Valeria Novelli, Mirella Memmi, Alberto Malovini, Andrea Mazzanti, Nian Liu, Ruan Yanfei, Rossana Bongianino, Marco Denegri, Nicola Monteforte, Raffaella Bloise, Massimo Morini, Carlo Napolitano
Publikováno v:
Heart rhythm. 19(5)
Evidence for the role of the CACNA1C gene, which encodes for the α-subunit of the cardiac L-type calcium channel CaV1.2, as a cause of the BrS3 variant of Brugada syndrome (BrS) is contradictory.The purpose of this study was to define in a large BrS
Autor:
Vern Hsen Tan, Yingjie Liu, S.R. Wayne Chen, Carlo Napolitano, Xiaowei Zhong, Jinhong Wei, Silvia G. Priori, Ruiwu Wang, Peter P. Jones, Yijun Tang, Lin Zhang, Wenting Guo, Joe Z. Zhang
Publikováno v:
Bioscience Reports
Mutations in cardiac ryanodine receptor (RyR2) are linked to catecholaminergic polymorphic ventricular tachycardia (CPVT). Most CPVT RyR2 mutations characterized are gain-of-function (GOF), indicating enhanced RyR2 function as a major cause of CPVT.
Autor:
Raffaella Bloise, Carlo Napolitano, Francesca La Rosa, Patrick Gambelli, Mirella Memmi, Antonio Curcio, Andrea Mazzanti, Alberto Malovini, Riccardo Bellazzi, Ciro Indolfi
Publikováno v:
Heart rhythm. 18(10)
Background The genetic architecture of Brugada syndrome (BrS) is emerging as an increasingly complex area of investigation. The identification of genetically homogeneous populations can provide mechanistic insights and improve genotype-phenotype corr
Autor:
Thomas M. Roston, Leif Hove-Madsen, Darrell D. Belke, Shubhayan Sanatani, Xiaowei Zhong, Janneke A.E. Kammeraad, Ruiwu Wang, Loryn J. Bohne, Jason D. Roberts, Ivan Blankoff, Wenting Guo, Arthur A.M. Wilde, Yong-Xiang Chen, S. R. Wayne Chen, Jinhong Wei, Carlo Napolitano, Alexander Vallmitjana, Johannes C. von Alvensleben, Lin Zhang, Robert A. Hegele, Julieta Lazarte, Raul Benitez, Mingke Ni, Robert A. Rose, Bo Sun, Krystien V.V. Lieve, Silvia G. Priori, Henrik Jensen, Jinjing Yao, Michael Fill, Anders Krogh Broendberg
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
instname
Science Translational Medicine, 13(579):eaba7287. American Association for the Advancement of Science
Sun, B, Yao, J, Ni, M, Wei, J, Zhong, X, Guo, W, Zhang, L, Wang, R, Belke, D, Chen, Y X, Lieve, K V V, Broendberg, A K, Roston, T M, Blankoff, I, Kammeraad, J A, Von Alvensleben, J C, Lazarte, J, Vallmitjana, A, Bohne, L J, Rose, R A, Benitez, R, Hove-Madsen, L, Napolitano, C, Hegele, R A, Fill, M, Sanatani, S, Wilde, A A M, Roberts, J D, Priori, S G, Jensen, H K & Chen, S R W 2021, ' Cardiac ryanodine receptor calcium release deficiency syndrome ', Science Translational Medicine, vol. 13, no. 579, eaba7287 . https://doi.org/10.1126/scitranslmed.aba7287
UPCommons. Portal del coneixement obert de la UPC
Universitat Politècnica de Catalunya (UPC)
Science Translational Medicine
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
Science translational medicine, 13(579):eaba7287. American Association for the Advancement of Science
instname
Science Translational Medicine, 13(579):eaba7287. American Association for the Advancement of Science
Sun, B, Yao, J, Ni, M, Wei, J, Zhong, X, Guo, W, Zhang, L, Wang, R, Belke, D, Chen, Y X, Lieve, K V V, Broendberg, A K, Roston, T M, Blankoff, I, Kammeraad, J A, Von Alvensleben, J C, Lazarte, J, Vallmitjana, A, Bohne, L J, Rose, R A, Benitez, R, Hove-Madsen, L, Napolitano, C, Hegele, R A, Fill, M, Sanatani, S, Wilde, A A M, Roberts, J D, Priori, S G, Jensen, H K & Chen, S R W 2021, ' Cardiac ryanodine receptor calcium release deficiency syndrome ', Science Translational Medicine, vol. 13, no. 579, eaba7287 . https://doi.org/10.1126/scitranslmed.aba7287
UPCommons. Portal del coneixement obert de la UPC
Universitat Politècnica de Catalunya (UPC)
Science Translational Medicine
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
Science translational medicine, 13(579):eaba7287. American Association for the Advancement of Science
Cardiac ryanodine receptor (RyR2) gain-of-function mutations cause catecholaminergic polymorphic ventricular tachycardia, a condition characterized by prominent ventricular ectopy in response to catecholamine stress, which can be reproduced on exerci