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van Spaendonck-Zwarts, KY, van Hessem, L, Jongbloed, JDH, de Walle, HEK, Capetanaki, Y, van der Kooi, AJ, van Langen, IM, van den Berg, MP, van Tintelen, JP
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Published in Clinical genetics (01.10.2011)
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Radonic, T, de Witte, P, Groenink, M, de Bruin-Bon, RACM, Timmermans, J, Scholte, AJH, van den Berg, MP, Baars, MJH, van Tintelen, JP, Kempers, M, Zwinderman, AH, Mulder, BJM
Published in Clinical genetics (01.10.2011)
Published in Clinical genetics (01.10.2011)
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Detection of genomic deletions of PKP2 in arrhythmogenic right ventricular cardiomyopathy
Roberts, JD, Herkert, JC, Rutberg, J, Nikkel, SM, Wiesfeld, ACP, Dooijes, D, Gow, RM, van Tintelen, JP, Gollob, MH
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Superior mesenteric artery aneurysm in a 9‐year‐old boy with classical Ehlers–Danlos syndrome
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Published in American journal of medical genetics. Part A (01.03.2012)
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Evaluation of left ventricular dimensions and function in Marfan's syndrome without significant valvular regurgitation
Meijboom, Lilian J., Timmermans, Janneke, van Tintelen, Johan P., Nollen, Gijs J., De Backer, Julie, van den Berg, Maarten P., Boers, Gerard H., Mulder, Barbara J.M.
Published in The American journal of cardiology (15.03.2005)
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Recurrent and founder mutations in the Netherlands—Phospholamban p.Arg14del mutation causes arrhythmogenic cardiomyopathy
van der Zwaag, P. A., van Rijsingen, I. A. W., de Ruiter, R., Nannenberg, E. A., Groeneweg, J. A., Post, J. G., Hauer, R. N. W., van Gelder, I. C., van den Berg, M. P., van der Harst, P., Wilde, A. A. M., van Tintelen, J. P.
Published in Netherlands heart journal (01.06.2013)
Published in Netherlands heart journal (01.06.2013)
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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
Sammani, A., Jansen, M., Linschoten, M., Bagheri, A., de Jonge, N., Kirkels, H., van Laake, L. W., Vink, A., van Tintelen, J. P., Dooijes, D., te Riele, A. S. J. M., Harakalova, M., Baas, A. F., Asselbergs, F. W.
Published in Netherlands heart journal (01.09.2019)
Published in Netherlands heart journal (01.09.2019)
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Rationale and design of the PHOspholamban RElated CArdiomyopathy intervention STudy (i-PHORECAST)
te Rijdt, W. P., Hoorntje, E. T., de Brouwer, R., Oomen, A., Amin, A., van der Heijden, J. F., Karper, J. C., Westenbrink, B. D., Silljé, H. H. W., te Riele, A. S. J. M., Wiesfeld, A. C. P., van Gelder, I. C., Willems, T. P., van der Zwaag, P. A., van Tintelen, J. P., Hillege, J. H., Tan, H. L., van Veldhuisen, D. J., Asselbergs, F. W., de Boer, R. A., Wilde, A. A. M., van den Berg, M. P.
Published in Netherlands heart journal (01.02.2022)
Published in Netherlands heart journal (01.02.2022)
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BIO FOr CARE: biomarkers of hypertrophic cardiomyopathy development and progression in carriers of Dutch founder truncating MYBPC3 variants—design and status
Jansen, M., Christiaans, I., van der Crabben, S. N., Michels, M., Huurman, R., Hoedemaekers, Y. M., Dooijes, D., Jongbloed, J. D. H., Boven, L. G., Lekanne Deprez, R. H., Wilde, A. A. M., Jans, J. J. M., van der Velden, J., de Boer, R. A., van Tintelen, J. P., Asselbergs, F. W., Baas, A. F.
Published in Netherlands heart journal (01.06.2021)
Published in Netherlands heart journal (01.06.2021)
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Haplotype sharing test maps genes for familial cardiomyopathies
van der Zwaag, PA, van Tintelen, JP, Gerbens, F, Jongbloed, JDH, Boven, LG, van der Smagt, JJ, van der Roest, WP, van Langen, IM, Bikker, H, Hauer, RNW, van den Berg, MP, Hofstra, RMW, te Meerman, GJ
Published in Clinical genetics (01.05.2011)
Published in Clinical genetics (01.05.2011)
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Risk stratification and subclinical phenotyping of dilated and/or arrhythmogenic cardiomyopathy mutation-positive relatives: CVON eDETECT consortium
Roudijk, R. W., Taha, K., Bourfiss, M., Loh, P., van den Heuvel, L., Boonstra, M. J., van Lint, F., van der Voorn, S. M., te Riele, A. S. J. M., Bosman, L. P., Christiaans, I., van Veen, T. A. B., Remme, C. A., van den Berg, M. P., van Tintelen, J. P., Asselbergs, F. W.
Published in Netherlands heart journal (01.06.2021)
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Neonatal lactic acidosis, complex I/IV deficiency, and fetal cerebral disruption
van Straaten, H L M, van Tintelen, J P, Trijbels, J M F, van den Heuvel, L P, Troost, D, Rozemuller, J M, Duran, M, de Vries, L S, Schuelke, M, Barth, P G
Published in Neuropediatrics (01.06.2005)
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Recurrent and founder mutations in the Netherlands: cardiac Troponin I (TNNI3) gene mutations as a cause of severe forms of hypertrophic and restrictive cardiomyopathy
van den Wijngaard, A., Volders, P., Van Tintelen, J. P., Jongbloed, J. D. H., van den Berg, M. P., Lekanne Deprez, R. H., Mannens, M. M. A. M., Hofmann, N., Slegtenhorst, M., Dooijes, D., Michels, M., Arens, Y., Jongbloed, R., Smeets, B. J. M.
Published in Netherlands heart journal (01.08.2011)
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Strength of patient cohorts and biobanks for cardiomyopathy research
de Boer, R. A., Nijenkamp, L. L. A. M., Silljé, H. H. W., Eijgenraam, T. R., Parbhudayal, R., van Driel, B., Huurman, R., Michels, M., Pei, J., Harakalova, M., van Lint, F. H. M., Jansen, M., Baas, A. F., Asselbergs, F. W., van Tintelen, J. P., Brundel, B. J. J. M., Dorsch, L. M., Schuldt, M., Kuster, D. W. D., van der Velden, J.
Published in Netherlands heart journal (01.08.2020)
Published in Netherlands heart journal (01.08.2020)
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The many faces of aggressive aortic pathology: Loeys-Dietz syndrome
Aalberts, J. J. J., van den Berg, M. P., Bergman, J. E. H., Sarvaas, G. J. du Marchie, Post, J. G., van Unen, H., Pals, G., Boonstra, P. W., van Tintelen, J. P.
Published in Netherlands heart journal (01.09.2008)
Published in Netherlands heart journal (01.09.2008)
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Auditory stimuli as a trigger for arrhythmic events differentiate HERG-related (LQTS2) patients from KVLQT1-related patients (LQTS1)
Wilde, Arthur A.M, Jongbloed, Rosalie J.E, Doevendans, Pieter A, Düren, Donald R, Hauer, Richard N.W, van Langen, Irene M, van Tintelen, J.Peter, Smeets, Hubert J.M, Meyer, Henk, Geelen, Jan L.M.C
Published in Journal of the American College of Cardiology (01.02.1999)
Published in Journal of the American College of Cardiology (01.02.1999)
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Otocephaly-Dysgnathia Complex: Description of Four Cases and Confirmation of the Role of OTX2
Patat, O., van Ravenswaaij-Arts, C.M.A., Tantau, J., Corsten-Janssen, N., van Tintelen, J.P., Dijkhuizen, T., Kaplan, J., Chassaing, N.
Published in Molecular syndromology (01.09.2013)
Published in Molecular syndromology (01.09.2013)
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Influence of stressful life events and personality traits on PLN cardiomyopathy severity: an exploratory study
van Drie, E, Taal, S E L, Schmidt, A F, Verstraelen, T E, de Brouwer, R, Schoormans, D, Mommersteeg, P M C, de Boer, R A, Wilde, A A M, Asselbergs, F W, Baas, A F, van Tintelen, J P, van den Heuvel, L M
Published in Europace (London, England) (28.12.2023)
Published in Europace (London, England) (28.12.2023)
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