Resultats de la cerca - J. Peter van Tintelen

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  1. 1
    The role of genetics in cardiovascular disease: arrhythmogenic cardiomyopathy

    The role of genetics in cardiovascular disease: arrhythmogenic cardiomyopathy per Cynthia A. James, Petros Syrris, J. Peter van Tintelen, Hugh Calkins

    Publicat 2020
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  2. 2
    Sex differences in cardiomyopathies

    Sex differences in cardiomyopathies per Sven Meyer, Peter van der Meer, J. Peter van Tintelen, Maarten P. van den Berg

    Publicat 2014
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  3. 3
    Fetal methotrexate syndrome: A systematic review of case reports

    Fetal methotrexate syndrome: A systematic review of case reports per Eline A. Verberne, Emma de Haan, J. Peter van Tintelen, Dick Lindhout, Mieke M. van Haelst

    Publicat 2019
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  4. 4
    Pregnancy, cardiomyopathies, and genetics

    Pregnancy, cardiomyopathies, and genetics per J. Peter van Tintelen, Petronella G. Pieper, Karin Y. van Spaendonck‐Zwarts, Maarten P. van den Berg

    Publicat 2014
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  5. 5
    Arrhythmogenic cardiomyopathy: pathology, genetics, and concepts in pathogenesis

    Arrhythmogenic cardiomyopathy: pathology, genetics, and concepts in pathogenesis per Edgar T. Hoorntje, Wouter P. te Rijdt, Cynthia A. James, Kalliopi Pilichou, Cristina Basso, Daniel P. Judge, Connie R. Bezzina, J. Peter van Tintelen

    Publicat 2017
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  6. 6
    The ARVD/C Genetic Variants Database: 2014 Update

    The ARVD/C Genetic Variants Database: 2014 Update per Elisabetta Lazzarini, Jan D.H. Jongbloed, Kalliopi Pilichou, Gaetano Thiene, Cristina Basso, Hennie Bikker, Bart Charbon, Morris A. Swertz, J. Peter van Tintelen, Paul A. van der Zwaag

    Publicat 2015
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  7. 7
    The RYR2-Encoded Ryanodine Receptor/Calcium Release Channel in Patients Diagnosed Previously With Either Catecholaminergic Polymorphic Ventricular Tachycardia or Genotype Negative, Exercise-Induced Long QT Syndrome

    The RYR2-Encoded Ryanodine Receptor/Calcium Release Channel in Patients Diagnosed Previously With Either Catecholaminergic Polymorphic Ventricular Tachycardia or Genotype Negative,... per 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

    Publicat 2009
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  8. 8
    Potential genetic predisposition for anthracycline-associated cardiomyopathy in families with dilated cardiomyopathy

    Potential genetic predisposition for anthracycline-associated cardiomyopathy in families with dilated cardiomyopathy per 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

    Publicat 2014
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  9. 9
    Prevalence and cardiac phenotype of patients with a phospholamban mutation

    Prevalence and cardiac phenotype of patients with a phospholamban mutation per 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

    Publicat 2018
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  10. 10
    Predicting arrhythmic risk in arrhythmogenic right ventricular cardiomyopathy: A systematic review and meta-analysis

    Predicting arrhythmic risk in arrhythmogenic right ventricular cardiomyopathy: A systematic review and meta-analysis per 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

    Publicat 2018
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  11. 11
    A systematic analysis of genetic dilated cardiomyopathy reveals numerous ubiquitously expressed and muscle‐specific genes

    A systematic analysis of genetic dilated cardiomyopathy reveals numerous ubiquitously expressed and muscle‐specific genes per 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

    Publicat 2015
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  12. 12
    A genetic variants database for arrhythmogenic right ventricular dysplasia/cardiomyopathy

    A genetic variants database for arrhythmogenic right ventricular dysplasia/cardiomyopathy per 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

    Publicat 2009
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  13. 13
    Peripartum Cardiomyopathy as a Part of Familial Dilated Cardiomyopathy

    Peripartum Cardiomyopathy as a Part of Familial Dilated Cardiomyopathy per 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

    Publicat 2010
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  14. 14
    High proportion of genetic cases in patients with advanced cardiomyopathy including a novel homozygous Plakophilin 2-gene mutation

    High proportion of genetic cases in patients with advanced cardiomyopathy including a novel homozygous Plakophilin 2-gene mutation per 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

    Publicat 2017
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  15. 15
    Auditory stimuli as a trigger for arrhythmic events differentiate HERG-related (LQTS2) patients from KVLQT1-related patients (LQTS1)

    Auditory stimuli as a trigger for arrhythmic events differentiate HERG-related (LQTS2) patients from KVLQT1-related patients (LQTS1) per 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

    Publicat 1999
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  16. 16
    Targeted Next-Generation Sequencing can Replace Sanger Sequencing in Clinical Diagnostics

    Targeted Next-Generation Sequencing can Replace Sanger Sequencing in Clinical Diagnostics per 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

    Publicat 2013
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  17. 17
    Expanding Spectrum of Human <i>RYR2</i> -Related Disease

    Expanding Spectrum of Human <i>RYR2</i> -Related Disease per 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

    Publicat 2007
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  18. 18
    UNRAVEL: big data analytics research data platform to improve care of patients with cardiomyopathies using routine electronic health records and standardised biobanking

    UNRAVEL: big data analytics research data platform to improve care of patients with cardiomyopathies using routine electronic health records and standardised biobanking per 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

    Publicat 2019
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  19. 19
    Prevalence and Disease Expression of Pathogenic and Likely Pathogenic Variants Associated With Inherited Cardiomyopathies in the General Population

    Prevalence and Disease Expression of Pathogenic and Likely Pathogenic Variants Associated With Inherited Cardiomyopathies in the General Population per 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

    Publicat 2022
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  20. 20
    Therapeutic efficacy of AAV-mediated restoration of PKP2 in arrhythmogenic cardiomyopathy

    Therapeutic efficacy of AAV-mediated restoration of PKP2 in arrhythmogenic cardiomyopathy per 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

    Publicat 2023
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