Zobrazeno 1 - 10 of 23 pro vyhledávání: '"Moniek G.P.J. Cox"'
1
Left-dominant arrhythmogenic cardiomyopathy in a large family: Associated desmosomal or nondesmosomal genotype?
Autor: Richard N.W. Hauer, Moniek G.P.J. Cox, Arnold Vreeker, Paul A. van der Zwaag, Toon A.B. van Veen, William J. McKenna, J. Peter van Tintelen, Dennis Dooijes, Jeroen F. van der Heijden, Judith A. Groeneweg, Jan D. H. Jongbloed, Rudolf A. de Boer
Publikováno v: Heart Rhythm, 10(4), 548-559. ELSEVIER SCIENCE INC
Background Arrhythmogenic cardiomyopathy (AC) is considered a predominantly right ventricular (RV) desmosomal disease. However, left-dominant forms due to desmosomal gene mutations, including PKP2 variant c.419C>T, have been described. Recently, a no
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::13a79ea856e2d1ff69ba4c8ad8f9a3b3
https://doi.org/10.1016/j.hrthm.2012.12.020
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2
Early Detection of Regional Functional Abnormalities in Asymptomatic ARVD/C Gene Carriers
Autor: Arco J. Teske, Bart W.L. De Boeck, Richard N.W. Hauer, Maarten J. Cramer, Anneline S.J.M. te Riele, Pieter A. Doevendans, Moniek G.P.J. Cox
Publikováno v: Journal of the American Society of Echocardiography. 25:997-1006
The overt stage of arrhythmogenic right ventricular (RV) dysplasia/cardiomyopathy (ARVD/C) is preceded by a concealed stage with minor or no signs of disease. However, sudden death may occur in this early phase. Deformation imaging may contribute to
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::257eaa9b83146e2367d6097cd9640bb2
https://doi.org/10.1016/j.echo.2012.05.008
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3
Clinical and Genetic Characterization of Patients with Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy Caused by a Plakophilin-2 Splice Mutation
Autor: Amber Ummels, Frans Gerbens, F. A. M. Hennekam, Paul A. van der Zwaag, Moniek G.P.J. Cox, Dennis Dooijes, Hennie Bikker, Arthur A.M. Wilde, J. Peter van Tintelen, Pieter A. Doevendans, Jasper J. van der Smagt, Irene M. van Langen, Richard N.W. Hauer
Publikováno v: Cardiology, 123(3), 181-189
Cardiology, 123(3), 181-189. S. Karger AG
Objectives: Arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C) is characterized by fibrofatty replacement of cardiomyocytes. In around 50% of index patients, a genetic predisposition is demonstrated. The purpose of this study was to e
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1c6ee4406967e7721942def72d7e2fa0
https://doi.org/10.1159/000342717
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5
Abstracts AB01-1 to AB21-5
Autor: Christian van der Werf, Jan D. H. Jongbloed, Maarten J. Cramer, Zahir A. Bhuiyan, Douwe E. Atsma, Irene M. van Langen, Ans C.P. Wiesfeld, Arjan C. Houweling, Maartje Noorman, Paul G.A. Volders, Jasper J. van der Smagt, Pieter A. Doevendans, Arthur A.M. Wilde, Dennis Dooijes, Paul A. van der Zwaag, Luc Jordaens, J. Peter van Tintelen, Moniek G.P.J. Cox, Arthur van den Wijngaard, Richard N.W. Hauer
Publikováno v: Heart Rhythm. 7:S1-S44
Introduction: Familial Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy (ARVD/C) is an autosomal dominantly inherited disease with incomplete penetrance and highly variable expression. Mutations in genes encoding 5 desmosomal proteins and TM
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::7ba1baefdf7b70829f3ae75c7ab59c99
https://doi.org/10.1016/j.hrthm.2010.03.028
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6
Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy Diagnostic Task Force Criteria Impact of New Task Force Criteria
Autor: Yvonne Arens, Moniek G.P.J. Cox, Maarten J. Cramer, Maartje Noorman, Pieter A. Doevendans, Jasper J. van der Smagt, Dennis Dooijes, Ans C.P. Wiesfeld, J. Peter van Tintelen, Richard N.W. Hauer, Paul G.A. Volders, Irene M. van Langen, Arjan C. Houweling, Arthur A.M. Wilde, Luc Jordaens, Peter Loh, Douwe E. Atsma
Publikováno v: Circulation. Arrhythmia and electrophysiology, 3(2), 126-133. Lippincott Williams and Wilkins
Circulation. Arrhythmia and Electrophysiology, 3(2), 126-133. LIPPINCOTT WILLIAMS & WILKINS
Circulation-Arrhythmia and Electrophysiology, 3(2), 126-133. LIPPINCOTT WILLIAMS & WILKINS
Circulation: Arrhythmia and Electrophysiology, 3(2), 126-133
Circulation-arrhythmia and electrophysiology, 3(2), 126-133. Lippincott Williams & Wilkins
Circulation. Arrhythmia and Electrophysiology, 3(2), 126-133. Lippincott Williams and Wilkins
Cox, M G P J, van der Smagt, J J, Noorman, M, Wiesfeld, A C, Volders, P G A, van Langen, I M, Atsma, D E, Dooijes, D, Houweling, A C, Loh, P, Jordaens, L, Arens, Y, Cramer, M J, Doevendans, P A, van Tintelen, P, Wilde, A A M & Hauer, R N W 2010, ' Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy Diagnostic Task Force Criteria Impact of New Task Force Criteria ', Circulation. Arrhythmia and Electrophysiology, vol. 3, no. 2, pp. 126-133 . https://doi.org/10.1161/CIRCEP.109.927202
Background— Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy (ARVD/C) Diagnostic Task Force Criteria (TFC) proposed in 1994 are highly specific but lack sensitivity. A new international task force modified criteria to improve diagnostic yi
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::658bfe17817b726583da25ed056af156
https://research.rug.nl/en/publications/e6cc3557-d199-4d91-9842-7707c833ed58
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7
Echocardiographic Tissue Deformation Imaging Quantifies Abnormal Regional Right Ventricular Function in Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy
Autor: Arco J. Teske, Maarten J. Cramer, Moniek G.P.J. Cox, Bart W.L. De Boeck, Richard N.W. Hauer, Pieter A. Doevendans
Publikováno v: Journal of the American Society of Echocardiography. 22:920-927
The aim of this study was to determine the accuracy of new quantitative echocardiographic strain and strain-rate imaging parameters to identify abnormal regional right ventricular (RV) deformation associated with arrhythmogenic right ventricular dysp
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6791b5e33025ee5373590b53440b7a57
https://doi.org/10.1016/j.echo.2009.05.014
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8
Cardiac cell–cell junctions in health and disease: Electrical versus mechanical coupling
Autor: Harold V.M. van Rijen, Maartje Noorman, Toon A.B. van Veen, Jacques M.T. de Bakker, Marcel A.G. van der Heyden, Richard N.W. Hauer, Moniek G.P.J. Cox
Publikováno v: Journal of Molecular and Cellular Cardiology. 47:23-31
Intercalated discs are the membrane sites where individual cardiomyocytes are connected to each other. Adherens-, desmosomal-, and gap junctions are situated in the intercalated disc and ensure mechanical coupling between cells and enable propagation
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d47013494b5708540187ecb382ebd20d
https://doi.org/10.1016/j.yjmcc.2009.03.016
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9
Activation delay and VT parameters in arrhythmogenic right ventricular dysplasia/cardiomyopathy: toward improvement of diagnostic ECG criteria
Autor: Peter Loh, Ans C.P. Wiesfeld, Moniek G.P.J. Cox, Jasper J. van der Smagt, J. Peter van Tintelen, Arthur A.M. Wilde, Pieter A. Doevendans, Jacques M.T. de Bakker, Maarten J. Cramer, Richard N.W. Hauer, Marcel R. Nelen
Publikováno v: Journal of cardiovascular electrophysiology, 19(8), 775-781. Wiley-Blackwell
Journal of Cardiovascular Electrophysiology, 19(8), 775-781. Wiley
Activation Delay and VT Parameters. Introduction: Desmosomal changes, electrical uncoupling, and surviving myocardial bundles embedded in fibrofatty tissue are hallmarks of activation delay in arrhythmogenic right ventricular dysplasia/cardiomyopathy
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::457e906dc9a3ba36ed1b66104967c7a6
https://doi.org/10.1111/j.1540-8167.2008.01140.x
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