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5 Most Recent Publications
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Recurrent and founder mutations in the Netherlands: The cardiac phenotype of DES founder mutations p.S13F and p.N342D
(Article)
Spaendonck-Zwarts, K.Y. van Kooi, A.J. van der Visser, M. de Jongbloed, J.D.H. Tintelen, J.P. van Berg, M.P. van den Ippel, E.F. Boven, L.G. Yee, W.C. Wijngaard, A. van den Brusse, E. Hoogendijk, J.E. Doevendans, P.A. |
2012-05-01
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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
(Article)
Wijngaard, A. van den Volders, P.G.A. Michels, M. Arens, Y.H.J.M. Smeets, B.J.M. Tintelen, J.P. van Jongbloed, J.D.H. Berg, M.P. van den Lekanne Deprez, R.H. Mannens, M.M.A.M. Hofmann, N. Slegtenhorst, M. Dooijes, D. |
2011-10-05
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Arrhythmogenic right ventricular dysplasia/cardiomyopathy: Pathogenic desmosome mutations in index-patients predict outcome of family screening: Dutch arrhythmogenic right ventricular dysplasia/cardiomyopathy genotype-phenotype follow-up study
(Article)
Cox, M.G.P.J. Zwaag, P.A. van der Wijngaard, A. van den Houweling, A.C. Jongbloed, J.D.H. Jordaens, L.J.L.M. Cramer, M.J. Doevendans, P.A. Bakker, J.M.T. de Wilde, A.A.M. Tintelen, J.P. van Hauer, R.N.W. Werf, C. van der Atsma, D.E. Smagt, J.J. van der Noorman, M. Bhuiyan, Z.A. Wiesfeld, A.C. Volders, P.G.A. Langen, I.M. van Dooijes, D. |
2011-06-14
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Response to letter regarding article, Peripartum cardiomyopathy as a part of familial dilated cardiomyopathy
(Article)
Spaendonck-Zwarts, K.Y. van Tintelen, J.P. van Jongbloed, J.D.H. Veldhuisen, D.J. van Werf, R. van der Berg, M.P. van den Paulus, W. Dooijes, D. |
2011-01-18
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Peripartum cardiomyopathy as a part of familial dilated cardiomyopathy
(Article)
Spaendonck-Zwarts, K.Y. van Tintelen, J.P. van Veldhuisen, D.J. van Werf, R. van der Jongbloed, J.D.H. Paulus, W.J. Dooijes, D. Berg, M.P. van den |
2010-05-25
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