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Ehjournal

Abstract Aims Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a rare genetic condition caused predominantly by mutations within desmosomal genes. Skin fibroblasts from a female and two ...

European Heart Journal, Milting, Hendrik, Klauke, Bärbel, Christensen, Alex Hoerby, Müsebeck, Jörg, Walhorn, Volker, Grannemann, Sören, Münnich, Tamara, Šarić, Tomo, Rasmussen, ...

Date : 07/04/2015
Ehjournal

Causes of dilated cardiomyopathy Dilated cardiomyopathy is currently defined by the presence of left ventricular (LV) or biventricular dilatation and systolic dysfunction in the absence of abnormal ...

European Heart Journal, Pinto, Yigal M., Elliott, Perry M., Arbustini, Eloisa, Adler, Yehuda, Anastasakis, Aris, Böhm, Michael, Duboc, Denis, Gimeno, Juan, de Groote, Pascal, Imazio, Massimo, ...

Date : 14/06/2016
Ehjournal

See page 1074 for the editorial comment on this article (doi:10.1093/eurheartj/ehu402) Translational Perspective We were able to show that targeted Next-Generation Sequencing is well suited to be ...

European Heart Journal, Haas, Jan, Frese, Karen S., Peil, Barbara, Kloos, Wanda, Keller, Andreas, Nietsch, Rouven, Feng, Zhu, Müller, Sabine, Kayvanpour, Elham, Vogel, Britta, Sedaghat-Hamedani, ...

Date : 07/05/2015 Item size : 433165 bytes
Ehjcardiovascrec

Abstract Aim Mutations in the RS-domain of RNA-binding motif protein 20 (RBM20) have recently been identified to segregate with aggressive forms of familial dilated cardiomyopathy (DCM). Titin ...

Cardiovascular Research, Beqqali, Abdelaziz, Bollen, Ilse A.E., Rasmussen, Torsten B., van den Hoogenhof, Maarten M., van Deutekom, Hanneke W.M., Schafer, Sebastian, Haas, Jan, Meder, Benjamin, ...

Date : 01/10/2016 Item size : 388685 bytes
Ehjcardiovascrec

Abstract Aim Mutations in the RS-domain of RNA-binding motif protein 20 (RBM20) have recently been identified to segregate with aggressive forms of familial dilated cardiomyopathy (DCM). Titin ...

Cardiovascular Research, Beqqali, Abdelaziz, Bollen, Ilse A.E., Rasmussen, Torsten B., van den Hoogenhof, Maarten M., van Deutekom, Hanneke W.M., Schafer, Sebastian, Haas, Jan, Meder, Benjamin, ...

Date : 01/10/2016 Item size : 390507 bytes
Ehjournal

Abstract Aims Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a rare genetic condition caused predominantly by mutations within desmosomal genes. Skin fibroblasts from a female and two ...

European Heart Journal, Milting, Hendrik, Klauke, Bärbel, Christensen, Alex Hoerby, Müsebeck, Jörg, Walhorn, Volker, Grannemann, Sören, Münnich, Tamara, Šarić, Tomo, Rasmussen, ...

Date : 07/04/2015 Item size : 454966 bytes
Ehjournal

See page 1074 for the editorial comment on this article (doi:10.1093/eurheartj/ehu402) Translational Perspective We were able to show that targeted Next-Generation Sequencing is well suited to be ...

European Heart Journal, Haas, Jan, Frese, Karen S., Peil, Barbara, Kloos, Wanda, Keller, Andreas, Nietsch, Rouven, Feng, Zhu, Müller, Sabine, Kayvanpour, Elham, Vogel, Britta, Sedaghat-Hamedani, ...

Date : 07/05/2015 Item size : 502689 bytes
Ehjournal

Abstract Aims Cardiomyopathies are a heterogeneous group of disorders associated with premature death due to ventricular arrhythmia or heart failure. Five hundred and seven (45.5%) patients ...

European Heart Journal, Elliott, Perry, Charron, Philippe, Blanes, Juan Ramon Gimeno, Tavazzi, Luigi, Tendera, Michal, Konté, Marème, Laroche, Cécile, Maggioni, Aldo P., Anastasakis, Aris, ...

Date : 07/01/2016 Item size : 392627 bytes
Ehjournal

Table 1 Aetiologies of dilated cardiomyopathy Group Subtype disease or agent Comments  Genetics  Main genes associated with predominant cardiac phenotype:        Titin ...

European Heart Journal, Pinto, Yigal M., Elliott, Perry M., Arbustini, Eloisa, Adler, Yehuda, Anastasakis, Aris, Böhm, Michael, Duboc, Denis, Gimeno, Juan, de Groote, Pascal, Imazio, Massimo, ...

Date : 14/06/2016 Item size : 407936 bytes