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Jordan, Elizabeth; Peterson, Laiken; Ai, Tomohiko; Asatryan, Babken; Bronicki, Lucas; Brown, Emily; Celeghin, Rudy; Edwards, Matthew; Fan, Judy; Ingles, Jodie; James, Cynthia A; Jarinova, Olga; Johnson, Renee; Judge, Daniel P; Lahrouchi, Najim; Lekanne Deprez, Ronald H; Lumbers, R Thomas; Mazzarotto, Francesco; Medeiros Domingo, Argelia; Miller, Rebecca L; ... (2021). Evidence-Based Assessment of Genes in Dilated Cardiomyopathy. Circulation, 144(1), pp. 7-19. American Heart Association 10.1161/CIRCULATIONAHA.120.053033
Sweda, Romy; Haeberlin, Andreas; Seiler, Jens; Servatius, Helge Simon; Noti, Fabian; Lam, Anna; Baldinger, Samuel Hannes; Goulouti, Eleni; Medeiros Domingo, Argelia; Fuhrer, Juerg; Reichlin, Tobias Roman; Roten, Laurent; Tanner, Hildegard (2019). How to Reach the Left Atrium in Atrial Fibrillation Ablation? Circulation. Arrhythmia and electrophysiology, 12(4), e006744. Lippincott Williams & Wilkins 10.1161/CIRCEP.118.006744
Lam, Anna; Bühler, Stefan Andreas; Goulouti, Eleni; Sweda, Romy; Haeberlin, Andreas; Medeiros Domingo, Argelia; Servatius, Helge Simon; Seiler, Jens; Baldinger, Samuel Hannes; Noti, Fabian; Tanner, Hildegard; Roten, Laurent (2019). Comparison of lead failure manifestation of Biotronik Linox with St. Jude Medical Riata and Medtronic Sprint Fidelis lead. Journal of interventional cardiac electrophysiology, 54(2), pp. 161-170. Springer 10.1007/s10840-018-0486-0
Asatryan, Babken; Schaller, André; Seiler, Jens; Servatius, Helge Simon; Noti, Fabian; Baldinger, Samuel H.; Tanner, Hildegard; Roten, Laurent; Dillier, Roger; Lam, Anna; Haeberlin, Andreas; Conte, Giulio; Saguner, Ardan M.; Müller, Stephan Andreas; Duru, Firat; Auricchio, Angelo; Ammann, Peter; Sticherling, Christian; Burri, Haran; Reichlin, Tobias; ... (2019). Usefulness of Genetic Testing in Sudden Cardiac Arrest Survivors With or Without Previous Clinical Evidence of Heart Disease. The American journal of cardiology, 123(12), pp. 2031-2038. Elsevier 10.1016/j.amjcard.2019.02.061
Chua, Han Chow; Servatius, Helge Simon; Asatryan, Babken; Schaller, André; Rieubland, Claudine; Noti, Fabian; Seiler, Jens; Roten, Laurent; Baldinger, Samuel Hannes; Tanner, Hildegard; Fuhrer, Jürg; Haeberlin, Andreas; Lam, Anna; Pless, Stephan A; Medeiros Domingo, Argelia (2018). Unexplained cardiac arrest: a tale of conflicting interpretations of KCNQ1 genetic test results. Clinical research in cardiology, 107(8), pp. 670-678. Springer-Verlag 10.1007/s00392-018-1233-3
Asatryan, Babken; Schaller, André; Bartholdi, Deborah; Medeiros Domingo, Argelia (2018). Late-onset severe long QT syndrome. Annals of noninvasive electrocardiology, 23(4), e12517. Wiley 10.1111/anec.12517
Akdis, D; Saguner, A M; Medeiros Domingo, Argelia; Schaller, André; Balmer, C; Steffel, J; Brunckhorst, C; Duru, F (2018). Multiple clinical profiles of families with the short QT syndrome. Europace, 20(FI1), f113-f121. Oxford University Press 10.1093/europace/eux186
Servatius, Helge Simon; Porro, Alessandro; Pless, Stephan A; Schaller, André; Asatryan, Babken; Tanner, Hildegard; de Marchi, Stefano F; Roten, Laurent; Seiler, Jens; Haeberlin, Andreas; Baldinger, Samuel Hannes; Noti, Fabian; Lam, Anna; Fuhrer, Jürg; Moroni, Anna; Medeiros Domingo, Argelia (2018). Phenotypic Spectrum of Mutations: A Clinical Case. Circulation. Genomic and precision medicine, 11(2), e002033. American Heart Association 10.1161/CIRCGEN.117.002033
Medeiros Domingo, Argelia; Bolliger, Stephan; Gräni, Christoph; Rieubland, Claudine; Hersch, Deborah; Asatryan, Babken; Schyma, Christian; Saguner, Ardan Muammer; Wyler, Daniel; Bhuiyan, Zahir; Fellman, Florence; Osculati, Antonio Marco; Ringger, Rebekka; Fokstuen, Siv; Sabatasso, Sara; Wilhelm, Matthias; Michaud, Katarzyna (2018). Recommendations for genetic testing and counselling after sudden cardiac death: practical aspects for Swiss practice. Swiss medical weekly, 148, w14638. EMH Schweizerischer Ärzteverlag 10.4414/smw.2018.14638
Bianchi, Beatrice; Ozhathil, Lijo Cherian; Medeiros Domingo, Argelia; Gollob, Michael H; Abriel, Hugues (2018). Four TRPM4 Cation Channel Mutations Found in Cardiac Conduction Diseases Lead to Altered Protein Stability. Frontiers in physiology, 9, p. 177. Frontiers Research Foundation 10.3389/fphys.2018.00177
Neubauer, Jaqueline; Lecca, MR; Russo, G; Bartsch, C; Medeiros Domingo, Argelia; Berger, Wolfgang; Haas, Cordula (2017). Post-mortem whole-exome analysis in a large sudden infant death syndrome cohort with a focus on cardiovascular and metabolic genetic diseases. European journal of human genetics, 25(4), pp. 404-409. Nature Publishing Group 10.1038/ejhg.2016.199
Neubauer, Jaqueline; Haas, Cordula; Bartsch, Christine; Medeiros Domingo, Argelia; Berger, Wolfgang (2016). Post-mortem whole-exome sequencing (WES) with a focus on cardiac disease-associated genes in five young sudden unexplained death (SUD) cases. International journal of legal medicine, 130(4), pp. 1011-1021. Springer 10.1007/s00414-016-1317-4
Medeiros Domingo, Argelia; Saguner, Ardan; Magyar, Istvan; Bahr, Angela; Akdis, Deniz; Brunckhorst, Corinna; Firat, Duru; Berger, Wolfgang (2016). Arrhythmogenic right ventricular cardiomyopathy: implications of next-generation sequencing in appropriate diagnosis. Europace, 19(6), pp. 1063-1069. Oxford University Press 10.1093/europace/euw098
Akdis, Deniz; Medeiros Domingo, Argelia; Gaertner-Rommel, Anna; Kast, Jeannette I; Enseleit, Frank; Bode, Peter; Klingel, Karin; Kandolf, Reinhard; Renois, Fanny; Andreoletti, Laurent; Akdis, Cezmi A; Milting, Hendrik; Lüscher, Thomas F; Brunckhorst, Corinna; Saguner, Ardan M; Duru, Firat (2016). Myocardial expression profiles of candidate molecules in patients with arrhythmogenic right ventricular cardiomyopathy/dysplasia compared to those with dilated cardiomyopathy and healthy controls. Heart rhythm, 13(3), pp. 731-741. Elsevier 10.1016/j.hrthm.2015.11.010
Noti, Fabian; Lam, Anna; Klossner, Nicole; Seiler, Jens; Servatius, Helge Simon; Medeiros Domingo, Argelia; Tran, van Nam; Haeberlin, Andreas; Fuhrer, Jürg; Tanner, Hildegard; Roten, Laurent (2016). Failure Rate and Conductor Externalization of the Biotronik Linox / Sorin Vigila Implantable Cardioverter Defibrillator Lead. Heart rhythm, 13(5), pp. 1075-1082. Elsevier 10.1016/j.hrthm.2015.12.038
Wilhelm, Matthias; Bolliger, Stephan A; Bartsch, Christine; Fokstuen, Siv; Gräni, Christoph; Martos, Viktor; Medeiros Domingo, Argelia; Osculati, Antonio; Rieubland, Claudine; Sabatasso, Sara; Saguner, Ardan Muammer; Schyma, Christian; Tschui, Joëlle; Wyler, Daniel; Bhuiyan, Zahurul A; Fellmann, Florence; Michaud, Katarzyna (2015). Sudden cardiac death in forensic medicine – Swiss recommendations for a multidisciplinary approach. Swiss medical weekly, 145, w14129. EMH Schweizerischer Ärzteverlag 10.4414/smw.2015.14129
Medeiros Domingo, Argelia; Tanner, Hildegard (2015). Das interessante EKG. EKG bei einem Kleinkind: gefährlich? Info@Herz+Gefäss, 2015(6), pp. 28-29. Aerzteverlag medinfo AG
Saguner, Ardan; Ganahl, Sabrina; Kraus, Andrea; Baldinger, Samuel Hannes; Medeiros Domingo, Argelia; Saguner, Arhan R; Mueller-Burri, Stephan; Wolber, Thomas; Haegeli, Laurent M; Nazmi, Krasniqi; Tanner, Felix C; Steffel, Jan; Brunckhorst, Corinna; Firat, Duru (2014). Clinical role of atrial arrhythmias in patients with arrhythmogenic right ventricular dysplasia. Circulation journal, 78(12), pp. 2854-2861. Japanese Circulation Society 10.1253/circj.CJ-14-0474
González-Melchor, Laila; Villarreal-Molina, Teresa; Iturralde-Torres, Pedro; Medeiros Domingo, Argelia (2014). Sudden cardiac death in individuals with normal hearts: an update. Archivos de cardiología de México, 84(4), pp. 293-304. Elsevier España 10.1016/j.acmx.2014.04.002
Arking, Dan E; Pulit, Sara L; Crotti, Lia; van der Harst, Pim; Munroe, Patricia B; Koopmann, Tamara T; Sotoodehnia, Nona; Rossin, Elizabeth J; Morley, Michael; Wang, Xinchen; Johnson, Andrew D; Lundby, Alicia; Gudbjartsson, Daníel F; Noseworthy, Peter A; Eijgelsheim, Mark; Bradford, Yuki; Tarasov, Kirill V; Dörr, Marcus; Müller-Nurasyid, Martina; Lahtinen, Annukka M; ... (2014). Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization. Nature genetics, 46(8), pp. 826-836. Nature America 10.1038/ng.3014
Saguner, Ardan Muammer; Ganahl, Sabrina; Baldinger, Samuel Hannes; Kraus, Andrea; Medeiros Domingo, Argelia; Nordbeck, Sebastian; Saguner, Arhan R; Mueller-Burri, Andreas S; Haegeli, Laurent M; Wolber, Thomas; Steffel, Jan; Krasniqi, Nazmi; Delacrétaz, Etienne; Lüscher, Thomas F; Held, Leonhard; Brunckhorst, Corinna B; Duru, Firat (2014). Usefulness of electrocardiographic parameters for risk prediction in arrhythmogenic right ventricular dysplasia. American journal of cardiology, 113(10), pp. 1728-1734. Elsevier 10.1016/j.amjcard.2014.02.031
Saguner, Ardan Muammer; Vecchiati, Alessandra; Baldinger, Samuel Hannes; Rüeger, Sina; Medeiros Domingo, Argelia; Mueller-Burri, Andreas S.; Haegeli, Laurent M; Biaggi, Patric; Manka, Robert; Lüscher, Thomas F.; Fontaine, Guy; Delacrétaz, Etienne; Jenni, Rolf; Held, Leonhard; Brunckhorst, Corinna; Duru, Firat; Tanner, Felix C. (2014). Different Prognostic Value of Functional Right Ventricular Parameters in Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia. Circulation. Cardiovascular Imaging, 7(2), pp. 230-239. Lippincott Williams & Wilkins 10.1161/CIRCIMAGING.113.000210
Medeiros Domingo, Argelia; Valdivia, Carmen R. (2014). Disease Caused by Mutations in NaV-β Subunit Genes. Cardiac Electrophysiology Clinics, 6(4), pp. 785-795. WB Saunders 10.1016/j.ccep.2014.08.008
Crotti, Lia; Marcou, Cherisse A; Tester, David J; Castelletti, Silvia; Giudicessi, John R; Torchio, Margherita; Medeiros Domingo, Argelia; Simone, Savastano; Will, Melissa L; Dagradi, Federica; Schwartz, Peter J; Ackerman, Michael J (2012). Spectrum and prevalence of mutations involving BrS1- through BrS12-susceptibility genes in a cohort of unrelated patients referred for Brugada syndrome genetic testing: implications for genetic testing. Journal of the American College of Cardiology, 60(15), pp. 1410-1418. Elsevier 10.1016/j.jacc.2012.04.037
Tester, David J.; Medeiros Domingo, Argelia; Will, Melissa L.; Haglund, Carla M.; Ackerman, Michael J. (2012). Cardiac channel molecular autopsy: insights from 173 consecutive cases of autopsy-negative sudden unexplained death referred for postmortem genetic testing. Mayo Clinic proceedings, 87(6), pp. 524-539. Elsevier 10.1016/j.mayocp.2012.02.017
Hu, Dan; Barajas-Martínez, Hector; Medeiros Domingo, Argelia; Crotti, Lia; Veltmann, Christian; Schimpf, Rainer; Urrutia, Janire; Alday, Aintzane; Casis, Oscar; Pfeiffer, Ryan; Burashnikov, Elena; Caceres, Gabriel; Tester, David J.; Wolpert, Christian; Borggrefe, Martin; Schwartz, Peter; Ackerman, Michael J.; Antzelevitch, Charles (2012). A novel rare variant in SCN1Bb linked to Brugada syndrome and SIDS by combined modulation of Na(v)1.5 and K(v)4.3 channel currents. Heart rhythm, 9(5), pp. 760-769. Elsevier 10.1016/j.hrthm.2011.12.006
Cheng, Jianding; Van Norstrand, David W.; Medeiros Domingo, Argelia; Tester, David J.; Valdivia, Carmen R.; Tan, Bi-Hua; Vatta, Matteo; Makielski, Jonathan C.; Ackerman, Michael J. (2011). LQTS-associated mutation A257G in α1-syntrophin interacts with the intragenic variant P74L to modify its biophysical phenotype. Cardiogenetics, 1(1) PAGEPress
Tester, David J.; Medeiros Domingo, Argelia; Will, Melissa L.; Ackerman, Michael J. (2011). Unexplained drownings and the cardiac channelopathies: a molecular autopsy series. Mayo Clinic proceedings, 86(10), pp. 941-947. Elsevier 10.4065/mcp.2011.0373
Tester, David J.; Tan, Bi-Hua; Medeiros Domingo, Argelia; Song, Chunhua; Makielski, Jonathan C.; Ackerman, Michael J. (2011). Loss-of-function mutations in the KCNJ8-encoded Kir6.1 K(ATP) channel and sudden infant death syndrome. Circulation - cardiovascular genetics, 4(5), pp. 510-515. Lippincott Williams & Wilkins 10.1161/CIRCGENETICS.111.960195
Medeiros Domingo, Argelia; Tan, Bi-Hua; Crotti, Lia; Tester, David J.; Eckhardt, Lee; Cuoretti, Alessandra; Kroboth, Stacie L.; Song, Chunhua; Zhou, Qing; Kopp, Doug; Schwartz, Peter J.; Makielski, Jonathan C; Ackerman, Michael J. (2010). Gain-of-function mutation S422L in the KCNJ8-encoded cardiac K(ATP) channel Kir6.1 as a pathogenic substrate for J-wave syndromes. Heart rhythm, 7(10), pp. 1466-1471. Elsevier 10.1016/j.hrthm.2010.06.016
Valdivia, Carmen R.; Medeiros Domingo, Argelia; Ye, Bin; Shen, Win-Kuang; Algiers, Timothy J.; Ackerman, Michael J.; Makielski, Jonathan C. (2010). Loss-of-function mutation of the SCN3B-encoded sodium channel {beta}3 subunit associated with a case of idiopathic ventricular fibrillation. Cardiovascular research, 86(3), pp. 392-400. Oxford University Press 10.1093/cvr/cvp417
Tan, Bi-Hua; Pundi, Kavitha N.; Van Norstrand, David W; Valdivia, Carmen R.; Tester, David J.; Medeiros Domingo, Argelia; Makielski, Jonathan C.; Ackerman, Michael J. (2010). Sudden infant death syndrome-associated mutations in the sodium channel beta subunits. Heart rhythm, 7(6), pp. 771-778. Elsevier 10.1016/j.hrthm.2010.01.032
Iturralde-Torres, Pedro; Medeiros Domingo, Argelia (2009). Genetic in long QT syndromes. Archivos de cardiología de México, 79 Suppl 2, pp. 26-30. Instituto Nacional de Cardiología Ignacio Chávez
Medeiros Domingo, Argelia (2009). Genetic of catecholaminergic polymorphic ventricular tachycardia: basic concepts. Archivos de cardiología de México, 79 Suppl 2, pp. 13-17. Instituto Nacional de Cardiología Ignacio Chávez
Cheng, Jianding; Van Norstrand, David W.; Medeiros Domingo, Argelia; Valdivia, Carmen; Tan, Bi-hua; Ye, Bin; Kroboth, Stacie; Vatta, Matteo; Tester, David J.; January, Craig T.; Makielski, Jonathan C.; Ackerman, Michael J. (2009). Alpha1-syntrophin mutations identified in sudden infant death syndrome cause an increase in late cardiac sodium current. Circulation. Arrhythmia and electrophysiology, 2(6), pp. 667-676. Lippincott Williams & Wilkins 10.1161/CIRCEP.109.891440
Medeiros Domingo, Argelia; Bhuiyan, Zahurul A.; Tester, David J.; Hofman, Nynke; Bikker, Hennie; van Tintelen, J. Peter; Mannens, Marcel M. A. M.; Wilde, Arthur A. M.; Ackerman, Michael J. (2009). The RYR2-encoded ryanodine receptor/calcium release channel in patients diagnosed previously with either catecholaminergic polymorphic ventricular tachycardia or genotype negative, exercise-induced long QT syndrome: a comprehensive open reading frame mutational analysis. Journal of the American College of Cardiology, 54(22), pp. 2065-2074. Elsevier 10.1016/j.jacc.2009.08.022
Medeiros Domingo, Argelia; Tan, Bi-Hua; Iturralde-Torres, Pedro; Tester, David J.; Tusié-Luna, Teresa; Makielski, Jonathan C.; Ackerman, Michael J. (2009). Unique mixed phenotype and unexpected functional effect revealed by novel compound heterozygosity mutations involving SCN5A. Heart rhythm, 6(8), pp. 1170-1175. Elsevier 10.1016/j.hrthm.2009.04.034
Ueda, Kazuo; Valdivia, Carmen; Medeiros Domingo, Argelia; Tester, David J.; Vatta, Matteo; Farrugia, Gianrico; Ackerman, Michael J.; Makielski, Jonathan C. (2008). Syntrophin mutation associated with long QT syndrome through activation of the nNOS-SCN5A macromolecular complex. Proceedings of the National Academy of Sciences of the United States of America - PNAS, 105(27), pp. 9355-9360. National Academy of Sciences NAS 10.1073/pnas.0801294105
Iturralde-Torres, Pedro; Nava-Townsend, Santiago; Gómez-Flores, Jorge; Medeiros Domingo, Argelia; Colín-Lizalde, Luis; Hermosillo, Antonio G.; Victoria, Diana; Márquez, Manlio F. (2008). Association of congenital, diffuse electrical disease in children with normal heart: sick sinus syndrome, intraventricular conduction block, and monomorphic ventricular tachycardia. Journal of cardiovascular electrophysiology, 19(5), pp. 550-555. Wiley-Blackwell 10.1111/j.1540-8167.2007.01006.x
Tan, Bi-Hua; Iturralde-Torres, Pedro; Medeiros Domingo, Argelia; Nava, Santiago; Tester, David J.; Valdivia, Carmen R.; Tusié-Luna, Teresa; Ackerman, Michael J.; Makielski, Jonathan C. (2007). A novel C-terminal truncation SCN5A mutation from a patient with sick sinus syndrome, conduction disorder and ventricular tachycardia. Cardiovascular research, 76(3), pp. 409-417. Oxford University Press 10.1016/j.cardiores.2007.08.006
Medeiros Domingo, Argelia; Kaku, Toshihiko; Tester, David J; Iturralde-Torres, Pedro; Itty, Ajit; Ye, Bin; Valdivia, Carmen; Ueda, Kazuo; Canizales-Quinteros, Samuel; Tusié-Luna, Maria Teresa; Makielski, Jonathan C.; Ackerman, Michael J. (2007). SCN4B-encoded sodium channel beta4 subunit in congenital long-QT syndrome. Circulation, 116(2), pp. 134-142. Lippincott Williams & Wilkins 10.1161/CIRCULATIONAHA.106.659086
Medeiros Domingo, Argelia; Iturralde-Torres, Pedro; Ackerman, Michael J. (2007). Clinical and genetic characteristics of long QT syndrome. Revista española de cardiología, 60(7), pp. 739-752. Elsevier
Canizales-Quinteros, S.; Aguilar-Salinas, C. A.; Ortiz-López, M. G.; Rodríguez-Cruz, M.; Villarreal-Molina, M. T.; Coral-Vázquez, R.; Huertas-Vázquez, A.; Hernández-Caballero, A.; López-Alarcón, M.; Brito-Zurita, O. R.; Domínguez-Banda, A.; Martinez-Sánchez, L. R.; Canto-de Cetina, T.; Vilchis-Dorantes, G.; Rosas-Vargas, H.; Granados-Silvestre, M. A.; Medeiros Domingo, Argelia; Menjivar, M.; Tusié-Luna, M. T. (2007). Association of PPARG2 Pro12Ala variant with larger body mass index in Mestizo and Amerindian populations of Mexico. Human biology, 79(1), pp. 111-119. Wayne State University Press
Medeiros Domingo, Argelia; Iturralde-Torres, Pedro; Canizales-Quinteros, Samuel; Hernández-Cruz, Arturo; Tusié-Luna, M. Teresa (2007). New perspectives in long QT syndrome. Revista de investigación clínica; organo del Hospital de Enfermedades de la Nutrición, 59(1), pp. 57-72. Instituto Nacional de la Nutricion "Salvador Zubiran"
Iturralde, Pedro; Nava, Santiago; Sálica, Gabriel; Medeiros Domingo, Argelia; Márquez, Manlio F.; Colin, Luis; Victoria, Diana; De Micheli, Alfredo; Gonzalez, Mario D. (2006). Electrocardiographic characteristics of patients with Ebstein's anomaly before and after ablation of an accessory atrioventricular pathway. Journal of cardiovascular electrophysiology, 17(12), pp. 1332-1336. Wiley-Blackwell 10.1111/j.1540-8167.2006.00617.x
Iturralde, Pedro; Guevara-Valdivia, Milton; Rodríguez-Chávez, Laura; Medeiros Domingo, Argelia; Colin, Luis (2002). Radiofrequency ablation of multiple accessory pathways. Europace, 4(3), pp. 273-280. Oxford University Press 10.1053/eupc.2002.0236
Timmermans, Carl; Rodriguez, Luz-Maria; Medeiros Domingo, Argelia; Crijns, Harry J. G. M.; Wellens, Hein J. J. (2002). Radiofrequency catheter ablation of idiopathic ventricular tachycardia originating in the main stem of the pulmonary artery. Journal of cardiovascular electrophysiology, 13(3), pp. 281-284. Wiley-Blackwell
Mendoza González, Celso; Iturralde Torres, Pedro; Medeiros Domingo, Argelia (2002). Electric therapy for heart failure. Archivos de cardiología de México, 72(4), pp. 350-359. Instituto Nacional de Cardiología Ignacio Chávez
Mendoza González, Celso; Iturralde Torres, Pedro; Guevara Valdivia, Milton E.; Medeiros Domingo, Argelia; Rodríguez Chávez, Laura; Rodríguez Briones, Ignacio; Colin Lizalde, Luis (2002). Follow-up of a group of patients with automatic implantable defibrillator. Archivos de cardiología de México, 72(3), pp. 220-226. Instituto Nacional de Cardiología Ignacio Chávez
Guevara-Valdivia, M. E.; Iturralde Torres, P.; de Micheli, A.; Colín Lizalde, L.; Medeiros Domingo, Argelia; González-Hermosillo, J. A. (2001). Electrocardiographic changes during stress test in a patient with "Brugada syndrome". Archivos de cardiología de México, 71(1), pp. 66-72. Instituto Nacional de Cardiología Ignacio Chávez
Cruz Cruz, F.; Iturralde Torres, P.; Picos Bovio, E.; Medeiros Domingo, Argelia; Infante Vázquez, O. (1998). The effectiveness and safety of d,l-sotalol in the ambulatory treatment of atrial fibrillation and flutter. Archivos del Instituto de Cardiología de México, 68(6), pp. 482-491. Instituto de Cardiología de México
Baldinger, Samuel Hannes; Shakir, Samera; Schmid, Michael; Roten, Laurent; Seiler, Jens; Noti, Fabian; Medeiros Domingo, Argelia; Fuhrer, Jürg; Tanner, Hildegard; Meier, Bernhard (2014). Concomitant atrial fibrillation ablation and left atrial appendage occlusion. Cardiovascular medicine - supplementum, Suppl23, p. 39. EMH Swiss Medical Publishers Ltd
