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10 Most Recent Publications
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Breakpoint mapping of 13 large parkin deletions/duplications reveals an exon 4 deletion and an exon 7 duplication as founder mutations
(Article)
Elfferich, P.C. Verleun-Mooijman, M.C. Swieten, J.C. van Boon, A.J.W. Engelen, K. van Verschuuren-Bemelmans, C.C. Lesnik-Oberstein, S.A.J. Tassorelli, C. Lopiano, L. Bonifati, V. Dooijes, D. Minkelen, R. van Maat-Kievit, A.A. Warrenburg, B. van de Abdo, W.F. Eshuis, S.A. Leenders, K.L. Hovestadt, A. Zijlmans, J.C.M. Stroy, J.-P.M. |
2011-11-01
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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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Manifest disease, risk factors for sudden cardiac death, and cardiac events in a large nationwide cohort of predictively tested hypertrophic cardiomyopathy mutation carriers: Determining the best cardiological screening strategy
(Article)
Christiaans, I. Birnie, E. Arens, Y.H.J.M. DenWijngaard, A. van Atsma, D.E. Helderman-van den Enden, A.T.J.M. Houweling, A.C. Boer, K. de Smagt, J.J. van der Hauer, R.N.W. Marcelis, C. Timmermans, J. Bonsel, G.J. Langen, I.M. van Wilde, A.A.M. Mannens, M.M.A.M. Michels, M. Majoor-Krakauer, D.F. Dooijes, D. Tintelen, J.P. van Berg, M.P. van den Volders, P.G.A. |
2011-05-01
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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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Erratum: Functional analysis of novel TBX5 T-box mutations associated with HoltOram syndrome (Cardiovascular Research (2010) 88:1 (130-139) DOI:101093/cvr/cvq178)
(Article)
Boogerd, C.J.J. Dooijes, D. Postma, A.V. Ilgun, A. Mathijssen, I.B. Hordijk, R. Laar, I.M.B.H. van de Rump, P. Veenstra-Knol, H.E. Moorman, A.F.M. Barnett, P. |
2011-01-01
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Functional analysis of novel TBX5 T-box mutations associated with Holt-Oram syndrome
(Article)
Boogerd, C.J.J. Dooijes, D. Ilgun, A. Hordijk, R. Laar, I.M.B.H. van de Rump, P. Veenstra-Knol, H.E. Moorman, A.F.M. Barnett, P. Postma, A.V. |
2010-10-01
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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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Polyalanine expansion in the ZIC3 gene leading to X-linked heterotaxy with VACTERL association: A new polyalanine disorder?
(Article)
Wessels, M.W. Kuchina, B. Casey, B. Heydanus, R. Smit, B.J. Dooijes, D. Krijger, R.R. de Lequin, M.H. Jong, E.M. de Husen, M. Willems, P.J. |
2010-05-01
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Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy Diagnostic Task Force Criteria impact of new Task Force Criteria
(Article)
Cox, M.G.P.J. Smagt, J.J. van der Jordaens, L.J.L.M. Arens, Y.H.J.M. Cramer, M.J. Doevendans, P.A. Tintelen, J.P. van Wilde, A.A.M. Hauer, R.N.W. Noorman, M. Wiesfeld, A.C. Volders, P.G.A. Langen, I.M. van Atsma, D.E. Dooijes, D. Houweling, A.C. Loh, P. |
2010-04-01
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