Publications by authors named "Argelia Medeiros-Domingo"

61Publications

Potential pro-arrhythmic effects of pharmacotherapy against SARS-CoV-2.

Arch Cardiol Mex 2020 ;90(Supl):36-40

Laboratorio de Arritmias. Departamento de Cardiología. Hospital Central Sur de Alta Especialidad Pemex. HCSAE, Ciudad de México/México.

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http://dx.doi.org/10.24875/ACM.M20000061DOI Listing
June 2020

Clinical predictors of left ventricular involvement in arrhythmogenic right ventricular cardiomyopathy.

Am Heart J 2020 05 7;223:34-43. Epub 2020 Feb 7.

Department of Cardiology, University Heart Center Zurich, Switzerland; Center for Integrative Human Physiology, University of Zurich, Zurich, Switzerland. Electronic address:

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http://dx.doi.org/10.1016/j.ahj.2020.01.019DOI Listing
May 2020

Functional characterization of a novel SCN5A variant associated with long QT syndrome and sudden cardiac death.

Int J Legal Med 2019 Nov 27;133(6):1733-1742. Epub 2019 Aug 27.

Department of Cardiology, Inselspital, University Hospital Bern, Bern, Switzerland.

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http://dx.doi.org/10.1007/s00414-019-02141-xDOI Listing
November 2019

Molecular and genetic insights into progressive cardiac conduction disease.

Europace 2019 Aug;21(8):1145-1158

Swiss DNAlysis, Adlerstrasse 1, Dübendorf, Switzerland.

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https://academic.oup.com/europace/advance-article/doi/10.109
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http://dx.doi.org/10.1093/europace/euz109DOI Listing
August 2019

How to Reach the Left Atrium in Atrial Fibrillation Ablation?: Patent Foramen Ovale Versus Transseptal Puncture.

Circ Arrhythm Electrophysiol 2019 04;12(4):e006744

Department of Cardiology, Inselspital, Bern University Hospital, Switzerland (R.S., A.H., J.S., H.S., F.N., A.L., S.B., E.G., A.M.-D., J.F., T.R., L.R., H.T.).

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http://dx.doi.org/10.1161/CIRCEP.118.006744DOI Listing
April 2019

Comparison of lead failure manifestation of Biotronik Linox with St. Jude Medical Riata and Medtronic Sprint Fidelis lead.

J Interv Card Electrophysiol 2019 Mar 23;54(2):161-170. Epub 2018 Nov 23.

Department of Cardiology, Inselspital, Bern University Hospital, University of Bern, Freiburgstrasse, 3010, Bern, Switzerland.

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http://dx.doi.org/10.1007/s10840-018-0486-0DOI Listing
March 2019

An autoantibody identifies arrhythmogenic right ventricular cardiomyopathy and participates in its pathogenesis.

Eur Heart J 2018 11;39(44):3932-3944

The Labatt Family Heart Centre (Department of Pediatrics) and Translational Medicine, The Hospital for Sick Children & Research Institute and the University of Toronto, Room 1725D, 555 University Avenue, Toronto, Ontario, Canada.

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http://dx.doi.org/10.1093/eurheartj/ehy567DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6247665PMC
November 2018

Translating emerging molecular genetic insights into clinical practice in inherited cardiomyopathies.

J Mol Med (Berl) 2018 10 20;96(10):993-1024. Epub 2018 Aug 20.

Department for Cardiology, Inselspital, Bern University Hospital, University of Bern, Freiburgstrasse 10, 3010, Bern, Switzerland.

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http://link.springer.com/10.1007/s00109-018-1685-y
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http://dx.doi.org/10.1007/s00109-018-1685-yDOI Listing
October 2018

Four TRPM4 Cation Channel Mutations Found in Cardiac Conduction Diseases Lead to Altered Protein Stability.

Front Physiol 2018 8;9:177. Epub 2018 Mar 8.

Swiss National Centre of Competence in Research (NCCR) TransCure, Institute of Biochemistry and Molecular Medicine, University of Bern, Bern, Switzerland.

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http://dx.doi.org/10.3389/fphys.2018.00177DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5852105PMC
March 2018

Emerging Implications of Genetic Testing in Inherited Primary Arrhythmia Syndromes.

Cardiol Rev 2019 Jan/Feb;27(1):23-33

From the Department of Cardiology, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.

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http://dx.doi.org/10.1097/CRD.0000000000000203DOI Listing
March 2019

Phenotypic Spectrum of Mutations: A Clinical Case.

Circ Genom Precis Med 2018 02;11(2):e002033

From the Department of Cardiology (H.S., B.A., H.T., S.F.d.M., L.R., J.S., A.H., S.H.B., F.N., A.L., J.F., A.M.-D.) and Division of Human Genetics, Department of Pediatrics (A.S.), Inselspital, Bern University Hospital, University of Bern, Switzerland; Artificial Organ Center for Biomedical Engineering Research, University of Bern, Switzerland (A.H.); Department of Biosciences, CNR IBF-Milano, Università degli Studi di Milano, Italy (A.P., A.M.); and Department of Drug Design and Pharmacology, Center for Biopharmaceuticals, University of Copenhagen, Denmark (S.A.P.).

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http://dx.doi.org/10.1161/CIRCGEN.117.002033DOI Listing
February 2018

Exome analysis in 34 sudden unexplained death (SUD) victims mainly identified variants in channelopathy-associated genes.

Int J Legal Med 2018 Jul 19;132(4):1057-1065. Epub 2018 Jan 19.

Zurich Institute of Forensic Medicine, Forensic Genetics, University of Zurich, Winterthurerstrasse 190/52, 8057, Zurich, Switzerland.

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http://dx.doi.org/10.1007/s00414-018-1775-yDOI Listing
July 2018

Late-onset severe long QT syndrome.

Ann Noninvasive Electrocardiol 2018 07 30;23(4):e12517. Epub 2017 Nov 30.

University Clinic of Cardiology, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.

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http://dx.doi.org/10.1111/anec.12517DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6931632PMC
July 2018

Arrhythmogenic right ventricular cardiomyopathy vs. dilated cardiomyopathy: implications for next-generation sequencing and microRNA regulation in appropriate diagnosis-Authors' reply.

Europace 2018 04;20(4):730

Department of Cardiology, University Hospital Bern, Freiburgstrasse 10, 3010 Bern, Switzerland.

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http://dx.doi.org/10.1093/europace/eux287DOI Listing
April 2018

Post-mortem whole-exome sequencing (WES) with a focus on cardiac disease-associated genes in five young sudden unexplained death (SUD) cases.

Int J Legal Med 2016 Jul 4;130(4):1011-1021. Epub 2016 Feb 4.

Institute of Medical Molecular Genetics, University of Zurich, Schlieren, Switzerland.

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http://dx.doi.org/10.1007/s00414-016-1317-4DOI Listing
July 2016

Failure rate and conductor externalization in the Biotronik Linox/Sorin Vigila implantable cardioverter-defibrillator lead.

Heart Rhythm 2016 05 29;13(5):1075-1082. Epub 2015 Dec 29.

Department of Cardiology, Inselspital, Bern University Hospital, and University of Bern, Bern, Switzerland. Electronic address:

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https://linkinghub.elsevier.com/retrieve/pii/S15475271150167
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http://dx.doi.org/10.1016/j.hrthm.2015.12.038DOI Listing
May 2016

Arrhythmogenic Left Ventricular Cardiomyopathy: Suspected by Cardiac Magnetic Resonance Imaging, Confirmed by Identification of a Novel Plakophilin-2 Variant.

Circulation 2015 Aug;132(6):e38-40

From Department of Cardiology, University Heart Center Zurich, Switzerland (A.M.S., R.M., A.G., C.B., F.D.); Department of Internal Medicine (B.B., K.A.M.) and Institute of Legal Medicine (D.W.), Cantonal Hospital of Grisons, Chur, Switzerland; and Department of Cardiology, University Hospital Bern, Switzerland (A.M.-D.).

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http://dx.doi.org/10.1161/CIRCULATIONAHA.115.017284DOI Listing
August 2015

[Sudden cardiac death in individuals with normal hearts: an update].

Arch Cardiol Mex 2014 Oct-Dec;84(4):293-304. Epub 2014 Aug 12.

Servicio de Arritmias, Hospital Universitario, Berna, Suiza. Electronic address:

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http://dx.doi.org/10.1016/j.acmx.2014.04.002DOI Listing
November 2015

Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization.

Authors:
Dan E Arking Sara L Pulit Lia Crotti Pim van der Harst Patricia B Munroe Tamara T Koopmann Nona Sotoodehnia Elizabeth J Rossin Michael Morley Xinchen Wang Andrew D Johnson Alicia Lundby Daníel F Gudbjartsson Peter A Noseworthy Mark Eijgelsheim Yuki Bradford Kirill V Tarasov Marcus Dörr Martina Müller-Nurasyid Annukka M Lahtinen Ilja M Nolte Albert Vernon Smith Joshua C Bis Aaron Isaacs Stephen J Newhouse Daniel S Evans Wendy S Post Daryl Waggott Leo-Pekka Lyytikäinen Andrew A Hicks Lewin Eisele David Ellinghaus Caroline Hayward Pau Navarro Sheila Ulivi Toshiko Tanaka David J Tester Stéphanie Chatel Stefan Gustafsson Meena Kumari Richard W Morris Åsa T Naluai Sandosh Padmanabhan Alexander Kluttig Bernhard Strohmer Andrie G Panayiotou Maria Torres Michael Knoflach Jaroslav A Hubacek Kamil Slowikowski Soumya Raychaudhuri Runjun D Kumar Tamara B Harris Lenore J Launer Alan R Shuldiner Alvaro Alonso Joel S Bader Georg Ehret Hailiang Huang W H Linda Kao James B Strait Peter W Macfarlane Morris Brown Mark J Caulfield Nilesh J Samani Florian Kronenberg Johann Willeit J Gustav Smith Karin H Greiser Henriette Meyer Zu Schwabedissen Karl Werdan Massimo Carella Leopoldo Zelante Susan R Heckbert Bruce M Psaty Jerome I Rotter Ivana Kolcic Ozren Polašek Alan F Wright Maura Griffin Mark J Daly David O Arnar Hilma Hólm Unnur Thorsteinsdottir Joshua C Denny Dan M Roden Rebecca L Zuvich Valur Emilsson Andrew S Plump Martin G Larson Christopher J O'Donnell Xiaoyan Yin Marco Bobbo Adamo P D'Adamo Annamaria Iorio Gianfranco Sinagra Angel Carracedo Steven R Cummings Michael A Nalls Antti Jula Kimmo K Kontula Annukka Marjamaa Lasse Oikarinen Markus Perola Kimmo Porthan Raimund Erbel Per Hoffmann Karl-Heinz Jöckel Hagen Kälsch Markus M Nöthen Marcel den Hoed Ruth J F Loos Dag S Thelle Christian Gieger Thomas Meitinger Siegfried Perz Annette Peters Hanna Prucha Moritz F Sinner Melanie Waldenberger Rudolf A de Boer Lude Franke Pieter A van der Vleuten Britt Maria Beckmann Eimo Martens Abdennasser Bardai Nynke Hofman Arthur A M Wilde Elijah R Behr Chrysoula Dalageorgou John R Giudicessi Argelia Medeiros-Domingo Julien Barc Florence Kyndt Vincent Probst Alice Ghidoni Roberto Insolia Robert M Hamilton Stephen W Scherer Jeffrey Brandimarto Kenneth Margulies Christine E Moravec Fabiola del Greco M Christian Fuchsberger Jeffrey R O'Connell Wai K Lee Graham C M Watt Harry Campbell Sarah H Wild Nour E El Mokhtari Norbert Frey Folkert W Asselbergs Irene Mateo Leach Gerjan Navis Maarten P van den Berg Dirk J van Veldhuisen Manolis Kellis Bouwe P Krijthe Oscar H Franco Albert Hofman Jan A Kors André G Uitterlinden Jacqueline C M Witteman Lyudmyla Kedenko Claudia Lamina Ben A Oostra Gonçalo R Abecasis Edward G Lakatta Antonella Mulas Marco Orrú David Schlessinger Manuela Uda Marcello R P Markus Uwe Völker Harold Snieder Timothy D Spector Johan Ärnlöv Lars Lind Johan Sundström Ann-Christine Syvänen Mika Kivimaki Mika Kähönen Nina Mononen Olli T Raitakari Jorma S Viikari Vera Adamkova Stefan Kiechl Maria Brion Andrew N Nicolaides Bernhard Paulweber Johannes Haerting Anna F Dominiczak Fredrik Nyberg Peter H Whincup Aroon D Hingorani Jean-Jacques Schott Connie R Bezzina Erik Ingelsson Luigi Ferrucci Paolo Gasparini James F Wilson Igor Rudan Andre Franke Thomas W Mühleisen Peter P Pramstaller Terho J Lehtimäki Andrew D Paterson Afshin Parsa Yongmei Liu Cornelia M van Duijn David S Siscovick Vilmundur Gudnason Yalda Jamshidi Veikko Salomaa Stephan B Felix Serena Sanna Marylyn D Ritchie Bruno H Stricker Kari Stefansson Laurie A Boyer Thomas P Cappola Jesper V Olsen Kasper Lage Peter J Schwartz Stefan Kääb Aravinda Chakravarti Michael J Ackerman Arne Pfeufer Paul I W de Bakker Christopher Newton-Cheh

Nat Genet 2014 Aug 22;46(8):826-36. Epub 2014 Jun 22.

1] Center for Human Genetic Research, Massachusetts General Hospital, Boston, Massachusetts, USA. [2] Program in Medical and Population Genetics, Broad Institute of Harvard and MIT, Cambridge, Massachusetts, USA. [3] Harvard Medical School, Boston, Massachusetts, USA. [4] Cardiovascular Research Center, Massachusetts General Hospital, Boston, Massachusetts, USA. [5].

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http://dx.doi.org/10.1038/ng.3014DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4124521PMC
August 2014

Usefulness of electrocardiographic parameters for risk prediction in arrhythmogenic right ventricular dysplasia.

Am J Cardiol 2014 May 2;113(10):1728-34. Epub 2014 Mar 2.

Department of Cardiology, University Heart Center Zurich, Zurich, Switzerland; Center for Integrative Human Physiology, University of Zurich, Zurich, Switzerland. Electronic address:

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http://dx.doi.org/10.1016/j.amjcard.2014.02.031DOI Listing
May 2014

LQTS-associated mutation A257G in α1-syntrophin interacts with the intragenic variant P74L to modify its biophysical phenotype.

Cardiogenetics 2011 Oct;1(1)

Division of Cardiovascular Medicine, Department of Medicine, University of Wisconsin, Madison, WI, USA ; Department of Forensic Pathology, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou, Guangdong, China.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3852898PMC
http://dx.doi.org/10.4081/cardiogenetics.2011.e13DOI Listing
October 2011

Unexplained drownings and the cardiac channelopathies: a molecular autopsy series.

Mayo Clin Proc 2011 Oct;86(10):941-7

Division of Cardiovascular Diseases, Mayo Clinic, Rochester, MN, USA.

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http://dx.doi.org/10.4065/mcp.2011.0373DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3184023PMC
October 2011

Loss-of-function mutations in the KCNJ8-encoded Kir6.1 K(ATP) channel and sudden infant death syndrome.

Circ Cardiovasc Genet 2011 Oct 11;4(5):510-5. Epub 2011 Aug 11.

Department of Medicine, Division of Cardiovascular Diseases, Windland Smith Rice Sudden Death Genomics Laboratory, Mayo Clinic, Rochester, MN 55905, USA.

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http://dx.doi.org/10.1161/CIRCGENETICS.111.960195DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3281577PMC
October 2011

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 2010 Oct 15;7(10):1466-71. Epub 2010 Jun 15.

Department of Medicine (Division of Cardiovascular Diseases), Windland Smith Rice Sudden Death Genomics Laboratory, Mayo Clinic, Rochester, Minnesota 55905, USA.

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http://dx.doi.org/10.1016/j.hrthm.2010.06.016DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3049900PMC
October 2010

[Genetic in long QT syndromes].

Arch Cardiol Mex 2009 Dec;79 Suppl 2:26-30

Servicio de Electrofisiología, Instituto Nacional de Cardiología Ignacio Chávez.

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December 2009

[Genetic of catecholaminergic polymorphic ventricular tachycardia: basic concepts].

Arch Cardiol Mex 2009 Dec;79 Suppl 2:13-7

Departamento de Medicina, División de Enfermedades Cardiovasculares, Mayo Clinic, Rochester, Minnesota, EUA.

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December 2009

Sudden infant death syndrome-associated mutations in the sodium channel beta subunits.

Heart Rhythm 2010 Jun 1;7(6):771-8. Epub 2010 Feb 1.

Department of Medicine, Cardiovascular Section, University of Wisconsin, Madison, Wisconsin, USA.

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http://dx.doi.org/10.1016/j.hrthm.2010.01.032DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2909680PMC
June 2010

Loss-of-function mutation of the SCN3B-encoded sodium channel {beta}3 subunit associated with a case of idiopathic ventricular fibrillation.

Cardiovasc Res 2010 Jun 30;86(3):392-400. Epub 2009 Dec 30.

Department of Medicine, Cardiovascular Section, and the Cardiac Molecular Arrhythmias Research Program, University of Wisconsin-Madison, 600 Highland Avenue H6/349, Madison, WI 53792, USA.

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http://dx.doi.org/10.1093/cvr/cvp417DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2868175PMC
June 2010

[Clinical and genetic characteristics of long QT syndrome].

Rev Esp Cardiol 2007 Jul;60(7):739-52

Unidad de Biología Molecular y Medicina Genómica, Instituto de Investigaciones Biomédicas, Universidad Nacional Autónoma de México.

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July 2007

[New perspectives in long QT syndrome].

Rev Invest Clin 2007 Jan-Feb;59(1):57-72

Unidad de Biología Molecular y Medicina Genómica, Instituto de Investigaciones Biomédicas.

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August 2007

[Electric therapy for heart failure].

Arch Cardiol Mex 2002 Oct-Dec;72(4):350-9

Departamento de Arritmias, Instituto Nacional de Cardiología Ignacio Chávez, INCICH, Juan Badiano No. 1, Col. Sección XVI, Delegación Tlalpan, 14080, México D.F.

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September 2003

[Follow-up of a group of patients with automatic implantable defibrillator].

Arch Cardiol Mex 2002 Jul-Sep;72(3):220-6

Departamento de Arritmias del Instituto Nacional de Cardiología Ignacio Chávez, INCICH, Juan Badiano No. 1, Col. Sección XVI, Tlalpan, 14080 México, D.F.

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December 2002