Výsledky vyhledávání - J. Peter van Tintelen
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Sex differences in cardiomyopathies Autor Sven Meyer, Peter van der Meer, J. Peter van Tintelen, Maarten P. van den Berg
Vydáno 2014Revisão -
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The RYR2-Encoded Ryanodine Receptor/Calcium Release Channel in Patients Diagnosed Previously With Either Catecholaminergic Polymorphic Ventricular Tachycardia or Genotype Negative,... Autor Argelia Medeiros‐Domingo, Zahurul A. Bhuiyan, David J. Tester, Nynke Hofman, Hennie Bikker, J. Peter van Tintelen, Marcel M.A.M. Mannens, Arthur A.M. Wilde, Michael J. Ackerman
Vydáno 2009Artigo -
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Potential genetic predisposition for anthracycline-associated cardiomyopathy in families with dilated cardiomyopathy Autor Marijke Wasielewski, Karin Y. van Spaendonck‐Zwarts, Nico-Derk L. Westerink, Jan D.H. Jongbloed, A. Postma, Jourik A. Gietema, J. Peter van Tintelen, Maarten P. van den Berg
Vydáno 2014Artigo -
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Prevalence and cardiac phenotype of patients with a phospholamban mutation Autor Irene E. Hof, Jeroen F. van der Heijden, Evangelia G. Kranias, Despina Sanoudou, Rudolf A. de Boer, J. Peter van Tintelen, Paul A. van der Zwaag, Pieter A. Doevendans
Vydáno 2018Revisão -
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Predicting arrhythmic risk in arrhythmogenic right ventricular cardiomyopathy: A systematic review and meta-analysis Autor Laurens P. Bosman, Arjan Sammani, Cynthia A. James, Julia Cadrin‐Tourigny, Hugh Calkins, J. Peter van Tintelen, Richard N.W. Hauer, Folkert W. Asselbergs, Anneline S.J.M. te Riele
Vydáno 2018Revisão -
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A systematic analysis of genetic dilated cardiomyopathy reveals numerous ubiquitously expressed and muscle‐specific genes Autor Magdaléna Harakaľová, Gijs J.M. Kummeling, Arjan Sammani, Marijke Linschoten, Annette F. Baas, Jasper van der Smagt, Pieter A. Doevendans, J. Peter van Tintelen, Dennis Dooijes, Michal Mokrý, Folkert W. Asselbergs
Vydáno 2015Artigo -
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A genetic variants database for arrhythmogenic right ventricular dysplasia/cardiomyopathy Autor Paul A. van der Zwaag, Jan D.H. Jongbloed, Maarten P. van den Berg, Jasper J. van der Smagt, Roselie Jongbloed, Hennie Bikker, Robert M.W. Hofstra, J. Peter van Tintelen
Vydáno 2009Artigo -
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Peripartum Cardiomyopathy as a Part of Familial Dilated Cardiomyopathy Autor Karin Y. van Spaendonck‐Zwarts, J. Peter van Tintelen, Dirk J. van Veldhuisen, Rik van der Werf, Jan D.H. Jongbloed, Walter J. Paulus, Dennis Dooijes, Maarten P. van den Berg
Vydáno 2010Artigo -
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High proportion of genetic cases in patients with advanced cardiomyopathy including a novel homozygous Plakophilin 2-gene mutation Autor Baerbel Klauke, Anna Gaertner, Uwe Schulz, Astrid Kassner, Edzard zu Knyphausen, T. Laser, Deniz Kececioglu, Lech Paluszkiewicz, Ute Blanz, Eugen Sandica, Antoon J. van den Bogaerdt, J. Peter van Tintelen, Jan Gummert, Hendrik Milting
Vydáno 2017Artigo -
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Auditory stimuli as a trigger for arrhythmic events differentiate HERG-related (LQTS2) patients from KVLQT1-related patients (LQTS1) Autor Arthur A.M. Wilde, Rosalie J.E. Jongbloed, Pieter A. Doevendans, Donald R. Düren, Richard N.W. Hauer, Irene M. van Langen, J. Peter van Tintelen, Hubert J.M. Smeets, H. Meyer, J. L. M. C. Geelen
Vydáno 1999Artigo -
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Targeted Next-Generation Sequencing can Replace Sanger Sequencing in Clinical Diagnostics Autor Birgit Sikkema‐Raddatz, Lennart Johansson, Eddy N. de Boer, Rowida Almomani, Ludolf G. Boven, Maarten P. van den Berg, Karin Y. van Spaendonck‐Zwarts, J. Peter van Tintelen, Rolf H. Sijmons, Jan D.H. Jongbloed, Richard J. Sinke
Vydáno 2013Artigo -
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Expanding Spectrum of Human <i>RYR2</i> -Related Disease Autor Zahurul A. Bhuiyan, Maarten P. van den Berg, J. Peter van Tintelen, Margreet Th.E. Bink‐Boelkens, Ans C.P. Wiesfeld, Mariëlle Alders, Alex V. Postma, Irene M. van Langen, Marcel M.A.M. Mannens, Arthur A.M. Wilde
Vydáno 2007Artigo -
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UNRAVEL: big data analytics research data platform to improve care of patients with cardiomyopathies using routine electronic health records and standardised biobanking Autor Arjan Sammani, M. Jansen, Marijke Linschoten, Ayoub Bagheri, Nicolaas de Jonge, Hans Kirkels, Linda W. van Laake, Aryan Vink, J. Peter van Tintelen, Dennis Dooijes, Anneline S.J.M. te Riele, Magdaléna Harakaľová, Annette F. Baas, Folkert W. Asselbergs
Vydáno 2019Artigo -
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Prevalence and Disease Expression of Pathogenic and Likely Pathogenic Variants Associated With Inherited Cardiomyopathies in the General Population Autor Mimount Bourfiss, Marion van Vugt, Abdulrahman Alasiri, Bram Ruijsink, Jessica van Setten, Amand F. 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
Vydáno 2022Artigo -
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Therapeutic efficacy of AAV-mediated restoration of PKP2 in arrhythmogenic cardiomyopathy Autor Eirini Kyriakopoulou, Daniëlle Versteeg, Hesther de Ruiter, Ilaria Perini, Fitzwilliam Seibertz, Yannic Döring, Lorena Zentilin, Hoyee Tsui, Sebastiaan J. van Kampen, Malte Tiburcy, Tim Meyer, Niels Voigt, J. Peter van Tintelen, Wolfram H. Zimmermann, Mauro Giacca, Eva van Rooij
Vydáno 2023Artigo
Vyhledávací nástroje:
Související témata
Medicine
Internal medicine
Heart failure
Biology
Cardiomyopathy
Genetics
Cardiology
Gene
Mutation
Arrhythmogenic right ventricular dysplasia
Dilated cardiomyopathy
Sudden cardiac death
Phenotype
Ventricular tachycardia
Bioinformatics
Disease
Ejection fraction
Genetic testing
Genotype
Hypertrophic cardiomyopathy
Sudden death
Environmental health
Implantable cardioverter-defibrillator
Missense mutation
Pathology
Penetrance
Population
Interquartile range
MYH7
Cohort