Search Results - van Tintelen, J. Peter
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A tailored approach towards informing relatives at risk of inherited cardiac conditions: study protocol for a randomised controlled trial by van den Heuvel, Lieke M, Hoedemaekers, Yvonne M, Baas, Annette F, van Tintelen, J Peter, Smets, Ellen M A, Christiaans, Imke
Published 2019Text -
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Autosomal dominant Marfan syndrome caused by a previously reported recessive FBN1 variant by Overwater, Eline, Efrat, Rifka, Barge‐Schaapveld, Daniela Q. C. M., Lakeman, Phillis, Weiss, Marjan M., Maugeri, Alessandra, van Tintelen, J. Peter, Houweling, Arjan C.
Published 2018Text -
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Follow-up care by a genetic counsellor for relatives at risk for cardiomyopathies is cost-saving and well-appreciated: a randomised comparison by Nieuwhof, Karin, Birnie, Erwin, van den Berg, Maarten P, de Boer, Rudolf A, van Haelst, Paul L, van Tintelen, J Peter, van Langen, Irene M
Published 2017Text -
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Uptake and Patient Perspectives on Additional Testing for Novel Disease-Associated Genes: Lessons from a PAH Cohort by Jansen, Samara M. A., van de Heuvel, Lieke M., Houweling, Arjan C., van Tintelen, J. Peter, de Man, Frances S., Vonk Noordegraaf, Anton, Jan Bogaard, Harm
Published 2021Text -
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A tailored approach to informing relatives at risk of inherited cardiac conditions: results of a randomised controlled trial by van den Heuvel, Lieke M., Hoedemaekers, Yvonne M., Baas, Annette F., Baars, Marieke J. H., van Tintelen, J. Peter, Smets, Ellen M. A., Christiaans, Imke
Published 2021Text -
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Long-Term Follow-Up Study on the Uptake of Genetic Counseling and Predictive DNA Testing in Inherited Cardiac Conditions by van den Heuvel, Lieke M., van Teijlingen, Maxiem O., van der Roest, Wilma, van Langen, Irene M., Smets, Ellen M.A., van Tintelen, J. Peter, Christiaans, Imke
Published 2020Text -
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Informing relatives at risk of inherited cardiac conditions: experiences and attitudes of healthcare professionals and counselees by van den Heuvel, Lieke M., Huisinga, Mette J., Hoedemaekers, Yvonne M., Baas, Annette F., Plantinga, Mirjam, Henneman, Lidewij, van Tintelen, J. Peter, Smets, Ellen M. A., Christiaans, Imke
Published 2019Text -
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Comprehensive Open Reading Frame Mutational Analysis of the RYR2-Encoded Ryanodine Receptor/Calcium Channel in Patients Diagnosed Previously with Either Catecholaminergic Polymorph... by Medeiros-Domingo, Argelia, Bhuiyan, Zahurul A., Tester, David J., Hofman, Nynke, Bikker, Hennie, van Tintelen, J Peter, Mannens, Marcel M.A.M, Wilde, Arthur A.M., Ackerman, Michael J.
Published 2009Text -
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Potential genetic predisposition for anthracycline-associated cardiomyopathy in families with dilated cardiomyopathy by Wasielewski, Marijke, van Spaendonck-Zwarts, Karin Y, Westerink, Nico-Derk L, Jongbloed, Jan D H, Postma, Aleida, Gietema, Jourik A, van Tintelen, J Peter, van den Berg, Maarten P
Published 2014Text -
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Quantitative Approach to Fragmented QRS in Arrhythmogenic Cardiomyopathy: From Disease towards Asymptomatic Carriers of Pathogenic Variants by Roudijk, Rob W., Bosman, Laurens P., van der Heijden, Jeroen F., de Bakker, Jacques M. T., Hauer, Richard N. W., van Tintelen, J. Peter, Asselbergs, Folkert W., te Riele, Anneline S. J. M., Loh, Peter
Published 2020Text -
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Terminal osseous dysplasia with pigmentary defects and cardiomyopathy caused by a novel FLNA variant by Rumping, Lynne, Wessels, Marja W., Postma, Alex V., van Schuppen, Joost, van Slegtenhorst, Marjon A., Saris, Jasper J., van Tintelen, J. Peter, Robertson, Stephen P., Alders, Mariëlle, Maas, Saskia M., Deprez, Ronald H. Lekanne
Published 2021Text -
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High proportion of genetic cases in patients with advanced cardiomyopathy including a novel homozygous Plakophilin 2-gene mutation by Klauke, Baerbel, Gaertner-Rommel, Anna, Schulz, Uwe, Kassner, Astrid, zu Knyphausen, Edzard, Laser, Thorsten, Kececioglu, Deniz, Paluszkiewicz, Lech, Blanz, Ute, Sandica, Eugen, van den Bogaerdt, Antoon J., van Tintelen, J. Peter, Gummert, Jan, Milting, Hendrik
Published 2017Text -
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Genetic Basis of Dilated Cardiomyopathy in Dogs and Its Potential as a Bidirectional Model by Gaar-Humphreys, Karen R., Spanjersberg, Talitha C. F., Santarelli, Giorgia, Grinwis, Guy C. M., Szatmári, Viktor, Roelen, Bernard A. J., Vink, Aryan, van Tintelen, J. Peter, Asselbergs, Folkert W., Fieten, Hille, Harakalova, Magdalena, van Steenbeek, Frank G.
Published 2022Text -
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Relevance of Titin Missense and Non-Frameshifting Insertions/Deletions Variants in Dilated Cardiomyopathy by Akinrinade, Oyediran, Heliö, Tiina, Lekanne Deprez, Ronald H., Jongbloed, Jan D. H., Boven, Ludolf G., van den Berg, Maarten P., Pinto, Yigal M., Alastalo, Tero-Pekka, Myllykangas, Samuel, Spaendonck-Zwarts, Karin van, van Tintelen, J. Peter, van der Zwaag, Paul A., Koskenvuo, Juha
Published 2019Text -
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Publisher Correction: Relevance of Titin Missense and Non-Frameshifting Insertions/Deletions Variants in Dilated Cardiomyopathy by Akinrinade, Oyediran, Heliö, Tiina, Lekanne Deprez, Ronald H., Jongbloed, Jan D. H., Boven, Ludolf G., van den Berg, Maarten P., Pinto, Yigal M., Alastalo, Tero-Pekka, Myllykangas, Samuel, van Spaendonck-Zwarts, Karin, van Tintelen, J. Peter, van der Zwaag, Paul A., Koskenvuo, Juha
Published 2020Text -
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Genetic Evaluation in a Cohort of 126 Dutch Pulmonary Arterial Hypertension Patients by van den Heuvel, Lieke M., Jansen, Samara M. A., Alsters, Suzanne I. M., Post, Marco C., van der Smagt, Jasper J., Handoko-De Man, Frances S., van Tintelen, J. Peter, Gille, Hans, Christiaans, Imke, Vonk Noordegraaf, Anton, Bogaard, HarmJan, Houweling, Arjan C.
Published 2020Text -
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Inflammation Aggravates Disease Severity in Marfan Syndrome Patients by Radonic, Teodora, de Witte, Piet, Groenink, Maarten, de Waard, Vivian, Lutter, Rene, van Eijk, Marco, Jansen, Marnix, Timmermans, Janneke, Kempers, Marlies, Scholte, Arthur J., Hilhorst-Hofstee, Yvonne, van den Berg, Maarten P., van Tintelen, J. Peter, Pals, Gerard, Baars, Marieke J. H., Mulder, Barbara J. M., Zwinderman, Aeilko H.
Published 2012Text -
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Identification of sarcomeric variants in probands with a clinical diagnosis of arrhythmogenic right ventricular cardiomyopathy (ARVC) by Murray, Brittney, Hoorntje, Edgar T., te Riele, Anneline S. J. M., Tichnell, Crystal, van der Heijden, Jeroen F., Tandri, Harikrishna, van den Berg, Maarten P., Jongbloed, Jan D. H., Wilde, Arthur A. M., Hauer, Richard N. W., Calkins, Hugh, Judge, Daniel P., James, Cynthia A., van Tintelen, J. Peter, Dooijes, Dennis
Published 2018Text