Kết quả tìm kiếm - van Tintelen, J. Peter

A tailored approach towards informing relatives at risk of inherited cardiac conditions: study protocol for a randomised controlled trial Bằng van den Heuvel, Lieke M, Hoedemaekers, Yvonne M, Baas, Annette F, van Tintelen, J Peter, Smets, Ellen M A, Christiaans, Imke

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Clinical utility gene card for: Dilated Cardiomyopathy (CMD) Bằng Posafalvi, Anna, Herkert, Johanna C, Sinke, Richard J, van den Berg, Maarten P, Mogensen, Jens, Jongbloed, Jan D H, van Tintelen, J Peter

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Clinical utility gene card for: arrhythmogenic right ventricular cardiomyopathy (ARVC) Bằng te Rijdt, Wouter P, Jongbloed, Jan DH, de Boer, Rudolf A, Thiene, Gaetano, Basso, Cristina, van den Berg, Maarten P, van Tintelen, J Peter

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Autosomal dominant Marfan syndrome caused by a previously reported recessive FBN1 variant Bằng Overwater, Eline, Efrat, Rifka, Barge‐Schaapveld, Daniela Q. C. M., Lakeman, Phillis, Weiss, Marjan M., Maugeri, Alessandra, van Tintelen, J. Peter, Houweling, Arjan C.

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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 Bằng 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

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Uptake and Patient Perspectives on Additional Testing for Novel Disease-Associated Genes: Lessons from a PAH Cohort Bằng 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

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A tailored approach to informing relatives at risk of inherited cardiac conditions: results of a randomised controlled trial Bằng 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

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Long-Term Follow-Up Study on the Uptake of Genetic Counseling and Predictive DNA Testing in Inherited Cardiac Conditions Bằng 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

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Informing relatives at risk of inherited cardiac conditions: experiences and attitudes of healthcare professionals and counselees Bằng 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

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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... Bằng 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.

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

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Quantitative Approach to Fragmented QRS in Arrhythmogenic Cardiomyopathy: From Disease towards Asymptomatic Carriers of Pathogenic Variants Bằng 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

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Terminal osseous dysplasia with pigmentary defects and cardiomyopathy caused by a novel FLNA variant Bằng 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

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

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Genetic Basis of Dilated Cardiomyopathy in Dogs and Its Potential as a Bidirectional Model Bằng 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.

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Relevance of Titin Missense and Non-Frameshifting Insertions/Deletions Variants in Dilated Cardiomyopathy Bằng 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

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Publisher Correction: Relevance of Titin Missense and Non-Frameshifting Insertions/Deletions Variants in Dilated Cardiomyopathy Bằng 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

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Genetic Evaluation in a Cohort of 126 Dutch Pulmonary Arterial Hypertension Patients Bằng 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.

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Inflammation Aggravates Disease Severity in Marfan Syndrome Patients Bằng 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.

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Identification of sarcomeric variants in probands with a clinical diagnosis of arrhythmogenic right ventricular cardiomyopathy (ARVC) Bằng 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

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