Zobrazeno 1 - 10
of 37
pro vyhledávání: '"Ferran Roses"'
Autor:
Paola Dolader, Iosune Alegria, Patricia Martínez Olorón, Joaquin Fernandez-Doblas, Ferran Gran, Ferran Roses-Noguer
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2022)
Hypertrophic cardiomyopathy is a heart muscle disease with an annual incidence between 0.24 and 0.47/100000 in childhood. Sudden cardiac death is the most common cause of death in this population. Although some medical treatment can decrease the risk
Externí odkaz:
https://doaj.org/article/ac54408d679c4354b9f47c6304486049
Publikováno v:
Anales de Pediatría, Vol 95, Iss 5, Pp 368-370 (2021)
Externí odkaz:
https://doaj.org/article/bbcce803d85644f7a66b3804c9acd3bb
Publikováno v:
Anales de Pediatría (English Edition), Vol 95, Iss 5, Pp 368-370 (2021)
Externí odkaz:
https://doaj.org/article/f9df0eeecd5146fa8fb01f609014e2a6
Autor:
Guiem Vaquer, Laura Marfil, Josep Ortega, Anna Sabate-Rotes, Ferran Gran-Ipina, Ferran Roses-Noguer
Publikováno v:
Annals of Pediatric Cardiology, Vol 13, Iss 3, Pp 264-266 (2020)
Flecainide is a class IC antiarrhythmic indicated for ventricular and supraventricular arrhythmias in pediatric patients without structural heart disease. Flecainide has a narrow therapeutic window and proarrhythmic effect even in therapeutic doses a
Externí odkaz:
https://doaj.org/article/c5fa0dcb39e9439e96f5a9262bffd37c
Autor:
Ivo Roca‐Luque, Nuria Rivas‐Gándara, Laura Dos‐Subirà, Jaume Francisco‐Pascual, Antònia Pijuan‐Domenech, Jordi Pérez‐Rodon, Alba Santos‐Ortega, Ferran Roses‐Noguer, Ignacio Ferreira‐Gonzalez, David García‐Dorado García, Angel Moya Mitjans
Publikováno v:
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, Vol 7, Iss 7 (2018)
BackgroundIntra‐atrial re‐entrant tachycardia (IART) in patients with congenital heart disease (CHD) increases morbidity and mortality. Radiofrequency catheter ablation has evolved as the first‐line treatment. The aim of this study was to analy
Externí odkaz:
https://doaj.org/article/899e224f6bb64c1a8e75621ad63736bd
Autor:
Michael A. Portman, Jeffrey P. Jacobs, Jane W. Newburger, Felix Berger, Michael A. Grosso, Anil Duggal, Ben Tao, Neil A. Goldenberg, Matthew Brothers, Bradley Marino, Charles Canter, Mark Law, Nguyenvu Nguyen, Charlie Sang, Kristin Shimano, Dipankar Gupta, Michael Portman, Derek Williams, Lauren Glass, Charles Sperrazza, Steven Herold, Ruchira Garg, Mark Vranicar, Sawsan Awad, Alfred Asante-Korang, Colleen Druzgal, Caroline Ozment, Kamill Del Toro, Ferran Roses, Christian Jux, Verena Gravenhorst, Ulrich Schweigmann, Mihir Bhatt, Christine Sabapathy, Nagib Dahdah, Dototea Bartonicek, Gerald Tulzer, Elena Basargina, Tatiana Zvereva, Tatiana Pertels, Irina Plotnikova, S.E.G.U.E.L.A. Pierre-Emmanuel, Pascal Amedro, Dulac Yves, Damien BONNET, Paola Saraco, Alessandro Rimini, Valerii Digtiar, Margaryta Gonchar, Tetyana Kryuchko, Olga Yablon, Varinder Singh Bedi, Jashvant Patel, Monjori Mitra, Jacek Kusa, Kowalczyk Domagala, László KÖRNYEI, Csaba BERECZKI, László ABLONCZY, Vivianne Aviva Levitas, David Mishali, Shoshana Revel-Vilk, Dan Harlev, Hatice Ilgen Sasmaz, Namik Yasar Ozbek, Sule Unal, Türkan Patıroglu, Baris Malbora, Hasan Agin, Zeynep Karakas, Ramazan Kaan Kavakli, Elizabeth Chalmers, Frances Bu'Lock, Piers Daubeney, Hala Hamza, Mohamed Badr, Mohsen Elalfy, Ahmed Mansour, Hoda Hassab, Ayman Sabry, Linda Daou, Fadi Bitar
Publikováno v:
Journal of the American College of Cardiology. 80:2301-2310
Standard of care (SOC) anticoagulation for thromboembolism (TE) prevention in children with cardiac disease includes low molecular weight heparins or vitamin K antagonists. Limited data exists for alternate use of direct oral anticoagulants in childr
Autor:
Roger Esmel-Vilomara, Irene Valenzuela, Lucia Riaza, Benjamin Rodriguez-Santiago, Ferran Roses-Noguer, Susana Boronat, Anna Sabate-Rotes
Arterial tortuosity syndrome (ATS) is an autosomal recessive connective tissue disease caused by biallelic variants in the SLC2A10gene and characterized by tortuosity and elongation of the aorta and medium-sized arteries. It’s considered an extreme
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cd38c84cef58065c9bbda7db13a319c0
https://doi.org/10.21203/rs.3.rs-2594978/v1
https://doi.org/10.21203/rs.3.rs-2594978/v1
Autor:
Puck J. Peltenburg, Dania Kallas, Johan M. Bos, Krystien V.V. Lieve, Sonia Franciosi, Thomas M. Roston, Isabelle Denjoy, Katrina B. Sorensen, Seiko Ohno, Ferran Roses-Noguer, Takeshi Aiba, Alice Maltret, Martin J. LaPage, Joseph Atallah, John R. Giudicessi, Sally-Ann B. Clur, Nico A. Blom, Michael Tanck, Fabrice Extramiana, Koichi Kato, Julien Barc, Martin Borggrefe, Elijah R. Behr, Georgia Sarquella-Brugada, Jacob Tfelt-Hansen, Esther Zorio, Heikki Swan, Janneke A.E. Kammeraad, Andrew D. Krahn, Andrew Davis, Frederic Sacher, Peter J. Schwartz, Jason D. Roberts, Jonathan R. Skinner, Maarten P. van den Berg, Prince J. Kannankeril, Fabrizio Drago, Tomas Robyns, Kristina Haugaa, Terezia Tavacova, Christopher Semsarian, Jan Till, Vincent Probst, Ramon Brugada, Wataru Shimizu, Minoru Horie, Antoine Leenhardt, Michael J. Ackerman, Shubhayan Sanatani, Christian van der Werf, Arthur A.M. Wilde
Publikováno v:
Circulation, 145(5), 333-344. Lippincott Williams & Wilkins
Circulation, 145(5), 333-344. Lippincott Williams and Wilkins
Peltenburg, P J, Kallas, D, Bos, J M, Lieve, K V V, Franciosi, S, Roston, T M, Denjoy, I, Sorensen, K B, Ohno, S, Roses-Noguer, F, Aiba, T, Maltret, A, Lapage, M J, Atallah, J, Giudicessi, J R, Clur, S-A B, Blom, N A, Tanck, M, Extramiana, F, Kato, K, Barc, J, Borggrefe, M, Behr, E R, Sarquella-Brugada, G, Tfelt-Hansen, J, Zorio, E, Swan, H, Kammeraad, J A E, Krahn, A D, Davis, A, Sacher, F, Schwartz, P J, Roberts, J D, Skinner, J R, van den Berg, M P, Kannankeril, P J, Drago, F, Robyns, T, Haugaa, K, Tavacova, T, Semsarian, C, Till, J, Probst, V, Brugada, R, Shimizu, W, Horie, M, Leenhardt, A, Ackerman, M J, Sanatani, S, van der Werf, C & Wilde, A A M 2022, ' An International Multicenter Cohort Study on β-Blockers for the Treatment of Symptomatic Children With Catecholaminergic Polymorphic Ventricular Tachycardia ', Circulation, vol. 145, no. 5, pp. 333-344 . https://doi.org/10.1161/CIRCULATIONAHA.121.056018
Circulation, 145(5), 333-344. LIPPINCOTT WILLIAMS & WILKINS
Circulation
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
instname
Circulation, 145(5), 333-344. Lippincott Williams and Wilkins
Peltenburg, P J, Kallas, D, Bos, J M, Lieve, K V V, Franciosi, S, Roston, T M, Denjoy, I, Sorensen, K B, Ohno, S, Roses-Noguer, F, Aiba, T, Maltret, A, Lapage, M J, Atallah, J, Giudicessi, J R, Clur, S-A B, Blom, N A, Tanck, M, Extramiana, F, Kato, K, Barc, J, Borggrefe, M, Behr, E R, Sarquella-Brugada, G, Tfelt-Hansen, J, Zorio, E, Swan, H, Kammeraad, J A E, Krahn, A D, Davis, A, Sacher, F, Schwartz, P J, Roberts, J D, Skinner, J R, van den Berg, M P, Kannankeril, P J, Drago, F, Robyns, T, Haugaa, K, Tavacova, T, Semsarian, C, Till, J, Probst, V, Brugada, R, Shimizu, W, Horie, M, Leenhardt, A, Ackerman, M J, Sanatani, S, van der Werf, C & Wilde, A A M 2022, ' An International Multicenter Cohort Study on β-Blockers for the Treatment of Symptomatic Children With Catecholaminergic Polymorphic Ventricular Tachycardia ', Circulation, vol. 145, no. 5, pp. 333-344 . https://doi.org/10.1161/CIRCULATIONAHA.121.056018
Circulation, 145(5), 333-344. LIPPINCOTT WILLIAMS & WILKINS
Circulation
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
instname
Background: Symptomatic children with catecholaminergic polymorphic ventricular tachycardia (CPVT) are at risk for recurrent arrhythmic events. β-Blockers decrease this risk, but studies comparing individual β-blockers in sizeable cohorts are lacki
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9763d1251c233799ab62ab359429a22b
https://openaccess.sgul.ac.uk/id/eprint/113944/1/CIRCULATIONAHA.121.056018.pdf
https://openaccess.sgul.ac.uk/id/eprint/113944/1/CIRCULATIONAHA.121.056018.pdf
Publikováno v:
Journal of Electrocardiology. 59:7-9
We report the first case of syncope with a documented asystole in a child triggered by hair grooming. No pathological findings were found, and a 15 s asystole event was recorded in an ambulatory 24 h electrocardiogram while her mother was combing her
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