Zobrazeno 1 - 10
of 38
pro vyhledávání: '"Mimount Bourfiss"'
Autor:
Lian Y. Rekker, Steven A. Muller, Alessio Gasperetti, Mimount Bourfiss, Marish I.F.J. Oerlemans, Maarten J. Cramer, Stefan L. Zimmerman, Dennis Dooijes, Hanke Schalkx, Pim van der Harst, Cynthia A. James, J. Peter van Tintelen, Marco Guglielmo, Birgitta K. Velthuis, Anneline S.J.M. te Riele
Publikováno v:
Journal of Cardiovascular Magnetic Resonance, Vol 26, Iss 2, Pp 101059- (2024)
ABSTRACT: Background: While late gadolinium enhancement (LGE) is proposed as a diagnostic criterion for arrhythmogenic right ventricular cardiomyopathy (ARVC), the potential of LGE to distinguish ARVC from differentials remains unknown. We aimed to a
Externí odkaz:
https://doaj.org/article/6c8027e8842f437fb6177ca748f9a36a
Autor:
Stephanie M. van der Voorn, Mimount Bourfiss, Steven A. Muller, Tolga Çimen, Ardan M. Saguner, Firat Duru, Anneline S. J. M. te Riele, Carol Ann Remme, Toon A. B. van Veen
Publikováno v:
Biomedicines, Vol 11, Iss 3, p 813 (2023)
Arrhythmogenic cardiomyopathy (ACM) is a progressive inheritable disease which is characterized by a gradual fibro-(fatty) replacement of the myocardium. Visualization of diffuse and patchy fibrosis patterns is challenging using clinically applied ca
Externí odkaz:
https://doaj.org/article/2101393d438542ce8aba94d19afeb921
Autor:
Stephanie M. van der Voorn, Mimount Bourfiss, Anneline S. J. M. te Riele, Karim Taha, Marc A. Vos, Remco de Brouwer, Tom E. Verstraelen, Rudolf A. de Boer, Carol Ann Remme, Toon A. B. van Veen
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 8 (2022)
Background: Pathogenic variants in phospholamban (PLN, like p. Arg14del), are found in patients diagnosed with arrhythmogenic (ACM) and dilated cardiomyopathy (DCM). Fibrosis formation in the heart is one of the hallmarks in PLN p.Arg14del carriers.
Externí odkaz:
https://doaj.org/article/6192dc2f457e4711a5d653f5b6215f1f
Autor:
Helen E. Driessen, Stephanie M. van der Voorn, Mimount Bourfiss, Freyja H. M. van Lint, Ferogh Mirzad, Laila El Onsri, Marc A. Vos, Toon A. B. van Veen
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 1, p 57 (2021)
In arrhythmogenic cardiomyopathy (ACM) pathogenic variants are found in genes encoding desmosomal proteins and in non-desmosomal genes, such as phospholamban (PLN, p.Arg14del variant). Previous research showed that plakoglobin protein levels and loca
Externí odkaz:
https://doaj.org/article/a80ab1536575421fbb61dc8705aee596
Autor:
Mimount Bourfiss, Davis M. Vigneault, Mounes Aliyari Ghasebeh, Brittney Murray, Cynthia A. James, Crystal Tichnell, Firdaus A. Mohamed Hoesein, Stefan L. Zimmerman, Ihab R. Kamel, Hugh Calkins, Harikrishna Tandri, Birgitta K. Velthuis, David A. Bluemke, Anneline S. J. M. te Riele
Publikováno v:
Journal of Cardiovascular Magnetic Resonance, Vol 19, Iss 1, Pp 1-13 (2017)
Abstract Background Regional right ventricular (RV) dysfunction is the hallmark of Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy (ARVD/C), but is currently only qualitatively evaluated in the clinical setting. Feature Tracking Cardiovascu
Externí odkaz:
https://doaj.org/article/02abd01b37ef4aeabe931bd28a96af77
Autor:
Amand F. Schmidt, Mimount Bourfiss, Abdulrahman Alasiri, Esther Puyol-Anton, Sandesh Chopade, Marion van Vugt, Sander W. van der Laan, Christian Gross, Chris Clarkson, Albert Henry, Tom R. Lumbers, Pim van der Harst, Nora Franceschini, Joshua C. Bis, Birgitta K. Velthuis, Anneline S. J. M. te Riele, Aroon D. Hingorani, Bram Ruijsink, Folkert W. Asselbergs, Jessica van Setten, Chris Finan
Publikováno v:
Science Advances. 9
Dysfunction of either the right or left ventricle can lead to heart failure (HF) and subsequent morbidity and mortality. We performed a genome-wide association study (GWAS) of 16 cardiac magnetic resonance (CMR) imaging measurements of biventricular
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
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
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
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
Autor:
Amand Schmidt, Chris Finan, Mimount Bourfiss, Birgitta Velthuis, Esther Puyol-Antón, Abdulrahman Alasiri, Bram Ruijsink, Folkert Asselbergs, Anneline ter Riele, Jessica van Setten
Background drug development and disease prevention of heart failure (HF) and atrial fibrillation (AF) are impeded by a lack of robust early-stage surrogates. We determined to what extent cardiac magnetic resonance (CMR) measurements act as surrogates
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3abf18893c3213011646fd1c93db4bcf
https://doi.org/10.21203/rs.3.rs-2449265/v1
https://doi.org/10.21203/rs.3.rs-2449265/v1
Autor:
Mimount Bourfiss, Marion van Vugt, Abdulrahman I. Alasiri, Bram Ruijsink, Jessica van Setten, A. Floriaan Schmidt, Dennis Dooijes, Esther Puyol-Antón, Birgitta K. Velthuis, J. Peter van Tintelen, Anneline S.J.M. te Riele, Annette F. Baas, Folkert W. Asselbergs
Publikováno v:
Circulation: Genomic and Precision Medicine. 15
Background: Pathogenic and likely pathogenic variants associated with arrhythmogenic right ventricular cardiomyopathy (ARVC), dilated cardiomyopathy (DCM), and hypertrophic cardiomyopathy (HCM) are recommended to be reported as secondary findings in