نتائج البحث - J. Peter van Tintelen
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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,... حسب 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
منشور في 2009Artigo -
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Potential genetic predisposition for anthracycline-associated cardiomyopathy in families with dilated cardiomyopathy حسب 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
منشور في 2014Artigo -
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Prevalence and cardiac phenotype of patients with a phospholamban mutation حسب 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
منشور في 2018Revisão -
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Predicting arrhythmic risk in arrhythmogenic right ventricular cardiomyopathy: A systematic review and meta-analysis حسب 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
منشور في 2018Revisão -
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A systematic analysis of genetic dilated cardiomyopathy reveals numerous ubiquitously expressed and muscle‐specific genes حسب 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
منشور في 2015Artigo -
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A genetic variants database for arrhythmogenic right ventricular dysplasia/cardiomyopathy حسب 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
منشور في 2009Artigo -
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Peripartum Cardiomyopathy as a Part of Familial Dilated Cardiomyopathy حسب 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
منشور في 2010Artigo -
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High proportion of genetic cases in patients with advanced cardiomyopathy including a novel homozygous Plakophilin 2-gene mutation حسب 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
منشور في 2017Artigo -
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Auditory stimuli as a trigger for arrhythmic events differentiate HERG-related (LQTS2) patients from KVLQT1-related patients (LQTS1) حسب 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
منشور في 1999Artigo -
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Targeted Next-Generation Sequencing can Replace Sanger Sequencing in Clinical Diagnostics حسب 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
منشور في 2013Artigo -
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Expanding Spectrum of Human <i>RYR2</i> -Related Disease حسب 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
منشور في 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 حسب 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
منشور في 2019Artigo -
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Prevalence and Disease Expression of Pathogenic and Likely Pathogenic Variants Associated With Inherited Cardiomyopathies in the General Population حسب 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
منشور في 2022Artigo -
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Therapeutic efficacy of AAV-mediated restoration of PKP2 in arrhythmogenic cardiomyopathy حسب 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
منشور في 2023Artigo
أدوات البحث:
موضوعات ذات صلة
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