Zobrazeno 1 - 10 of 243 pro vyhledávání: '"Maarten P. Van Den Berg"'
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Akademický článek
Diagnostic Performance of Various QTc Interval Formulas in a Large Family with Long QT Syndrome Type 3: Bazett's Formula Not So Bad After All …
Autor: Jan Brouwer, Maarten P. Van Den Berg, Diederick E. Grobbee, Jaap Haaksma, Arthur A.M. Wilde
Publikováno v: Annals of Noninvasive Electrocardiology, Vol 8, Iss 4, Pp 269-274 (2003)
Background: Recently, we identified a novel mutation of SCN5A (1795insD) in a large family with LQTS3. The aim of this study was to assess whether the various proposed corrections of the QT interval to heart rate help to improve the identification of
Externí odkaz: https://doaj.org/article/bcb5fe3026f64fa1ba4f03b2c0df4f6f
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2
Akademický článek
Cardiac Transthyretin-derived Amyloidosis: An Emerging Target in Heart Failure with Preserved Ejection Fraction?
Autor: Sebastiaan HC Klaassen, Dirk J van Veldhuisen, Hans LA Nienhuis, Maarten P van den Berg, Bouke PC Hazenberg, Peter van der Meer
Publikováno v: Cardiac Failure Review, Vol 6, Iss , Pp - (2020)
Heart failure with preserved ejection fraction (HFpEF) comprises half of the heart failure population. A specific, but underdiagnosed, cause for HFpEF is transthyretin-derived (ATTR) amyloidosis. This article reviews the clinical characteristics of c
Externí odkaz: https://doaj.org/article/95b6495b7e1045f9870bb1ae57637de7
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4
Akademický článek
Heritability in genetic heart disease: the role of genetic background
Autor: Yigal M Pinto, Joeri A Jansweijer, Karin Y van Spaendonck-Zwarts, Michael W T Tanck, J Peter van Tintelen, Imke Christiaans, J Martijn Bos, Arthur J Moss, Heikki Swan, Annika Rydberg, Jacob Tfelt-Hansen, Iacopo Olivotto, Philippe Charron, Juan R Gimeno, Maarten P van den Berg, Jasper J van der Smagt, Alexa M C Vermeer, Sylvia G Priori, Michael J Ackerman, Arthur AM Wilde
Publikováno v: Open Heart, Vol 6, Iss 1 (2019)
Background Mutations in genes encoding ion channels or sarcomeric proteins are an important cause of hereditary cardiac disease. However, the severity of the resultant disease varies considerably even among those with an identical mutation. Such clin
Externí odkaz: https://doaj.org/article/d80eef2a41b34518888d3b17f89ded1b
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6
Clinical Characteristics and Follow-Up of Pediatric-Onset Arrhythmogenic Right Ventricular Cardiomyopathy
Autor: Robert W. Roudijk, Lisa Verheul, Laurens P. Bosman, Mimount Bourfiss, Johannes M.P.J. Breur, Martijn G. Slieker, Andreas C. Blank, Dennis Dooijes, Jeroen F. van der Heijden, Freek van den Heuvel, Sally-Ann Clur, Floris E.A. Udink ten Cate, Maarten P. van den Berg, Arthur A.M. Wilde, Folkert W. Asselbergs, J. Peter van Tintelen, Anneline S.J.M. te Riele
Publikováno v: Roudijk, R W, Verheul, L, Bosman, L P, Bourfiss, M, Breur, J M P J, Slieker, M G, Blank, A C, Dooijes, D, van der Heijden, J F, van den Heuvel, F, Clur, S-A, Udink ten Cate, F E A, van den Berg, M P, Wilde, A A M, Asselbergs, F W, Peter van Tintelen, J & te Riele, A S J M 2022, ' Clinical Characteristics and Follow-Up of Pediatric-Onset Arrhythmogenic Right Ventricular Cardiomyopathy ', JACC: Clinical Electrophysiology, vol. 8, no. 3, pp. 306-318 . https://doi.org/10.1016/j.jacep.2021.09.001
JACC: Clinical Electrophysiology, 8(3), 306-318. Elsevier USA
JACC. Clinical electrophysiology, 8(3), 306-318. Elsevier
JACC. Clinical Electrophysiology, 8, 306-318
JACC. Clinical Electrophysiology, 8, 3, pp. 306-318
Objectives: The goal of this study was to describe characteristics, cascade screening results, and predictors of adverse outcome in pediatric-onset arrhythmogenic right ventricular cardiomyopathy (ARVC). Background: Although ARVC is increasingly reco
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5e869353bfb8bda89957d2e6400c1a9d
https://doi.org/10.1016/j.jacep.2021.09.001
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7
Comparing clinical performance of current implantable cardioverter-defibrillator implantation recommendations in arrhythmogenic right ventricular cardiomyopathy
Autor: Anneline S.J.M. te Riele, Cynthia A. James, Julia Cadrin-Tourigny, Folkert W. Asselbergs, Laurens P Bosman, Claire L Nielsen Gerlach, Sing-Chien Yap, Katja Zeppenfeld, Brittney Murray, Gabriela M. Orgeron, Hariskrishna Tandri, Arthur A.M. Wilde, Hugh Calkins, Mimount Bourfiss, Crystal Tichnell, Maarten P. van den Berg, J. Peter van Tintelen, Jeroen F. van der Heijden
Publikováno v: Europace, 24(2):euab162, 296-305. Oxford University Press
EP Europace, 24(2), 296-305. Oxford University Press
Europace, 24(2), 296-305. Oxford University Press
EP Europace, 24(2), 296-305. OXFORD UNIV PRESS
Aims Arrhythmogenic right ventricular cardiomyopathy (ARVC) patients have an increased risk of ventricular arrhythmias (VA). Four implantable cardioverter-defibrillator (ICD) recommendation algorithms are available The International Task Force Consen
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6302f4d1c5023eb402e12d69fdca001d
https://doi.org/10.1093/europace/euab162
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9
TAB2 deletions and variants cause a highly recognisable syndrome with mitral valve disease, cardiomyopathy, short stature and hypermobility
Autor: Aafke Engwerda, Maarten P. van den Berg, Wilhelmina S. Kerstjens-Frederikse, Yvonne J. Vos, Bert B.A. de Vries, Tuula Rinne, Marc T R Roofthooft, Paulien A Terhal, Patrick Deelen, Conny M. A. van Ravenswaaij-Arts, Barbara Frentz, Katharina Löhner, Trijnie Dijkhuizen, Erika Leenders
Publikováno v: European Journal of Human Genetics, 29, 1669-1676. Nature Publishing Group
Eur J Hum Genet
Deletions that include the gene TAB2 and TAB2 loss-of-function variants have previously been associated with congenital heart defects and cardiomyopathy. However, other features, including short stature, facial dysmorphisms, connective tissue abnorma
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1fd540b65f880419358b12d518f7ffd4
https://doi.org/10.1038/s41431-021-00948-0
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10
Variant Location Is a Novel Risk Factor for Individuals With Arrhythmogenic Cardiomyopathy Due to a Desmoplakin (DSP) Truncating Variant
Autor: Edgar T. Hoorntje, Charlotte Burns, Luisa Marsili, Ben Corden, Victoria N. Parikh, Gerard J. te Meerman, Belinda Gray, Ahmet Adiyaman, Richard D. Bagnall, Daniela Q.C.M. Barge-Schaapveld, Maarten P. van den Berg, Marianne Bootsma, Laurens P. Bosman, Gemma Correnti, Johan Duflou, Ruben N. Eppinga, Diane Fatkin, Michael Fietz, Eric Haan, Jan D.H. Jongbloed, Arnaud D. Hauer, Lien Lam, Freyja H.M. van Lint, Amrit Lota, Carlo Marcelis, Hugh J. McCarthy, Anneke M. van Mil, Rogier A. Oldenburg, Nicholas Pachter, R. Nils Planken, Chloe Reuter, Christopher Semsarian, Jasper J. van der Smagt, Tina Thompson, Jitendra Vohra, Paul G.A. Volders, Jaap I. van Waning, Nicola Whiffin, Arthur van den Wijngaard, Ahmad S. Amin, Arthur A.M. Wilde, Gijs van Woerden, Laura Yeates, Dominica Zentner, Euan A. Ashley, Matthew T. Wheeler, James S. Ware, J. Peter van Tintelen, Jodie Ingles
Publikováno v: Circulation. Genomic and Precision Medicine, 16, 1
Circulation: Genomic and Precision Medicine, 16(1):E003672. LIPPINCOTT WILLIAMS & WILKINS
Circulation. Genomic and precision medicine, 16(1). Lippincott Williams and Wilkins Ltd.
Circulation: Genomic and Precision Medicine, 16(1), 69-79. Lippincott Williams and Wilkins Ltd.
Circulation. Genomic and Precision Medicine, 16
Circulation: Genomic and Precision Medicine, 16(1). Lippincott Williams & Wilkins
Background: Truncating variants in desmoplakin ( DSP tv) are an important cause of arrhythmogenic cardiomyopathy; however the genetic architecture and genotype-specific risk factors are incompletely understood. We evaluated phenotype, risk factors fo
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::168e6f2d791aa1fd96556c202c710360
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