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Rickert-Sperling 01. Januar 2016 Human genetics of ventricular septal defect K. Bellmann A. Perrot S. Rickert-Sperling 01. Januar 2016 Preface S. Rickert-Sperling R.G. Kelly D.J. Driscoll 01. Januar 2016 Congenital heart diseases: the broken heart : clinical features, human genetics and molecular pathways S. Rickert-Sperling R.G. Kelly D.J. Driscoll 01. Januar 2016 Cardiac transcription factors and regulatory networks M. Grunert C. Dorn S. Rickert-Sperling 01. Januar 2016 Human genetics of tetralogy of fallot and double outlet right ventricle C. Dorn A. Perrot S. Rickert-Sperling 01. Januar 2016 Technologies to study genetics and molecular pathways C. Dorn M. Grunert A. Dopazo F. Sanchez-Cabo A. Gatto J. Vazquez S. Rickert-Sperling E. Lara-Pezzi 01. Februar 2016 / Cardiovasc Res Congenital coronary artery anomalies: a bridge from embryology to anatomy and pathophysiology-a position statement of the development, anatomy, and pathology ESC Working Group J.M. Perez-Pomares J.L. de la Pompa D. Franco D. Henderson S.Y. Ho L. Houyel R.G. Kelly D. Sedmera M. Sheppard S. Sperling G. Thiene M. van den Hoff C. Basso 01. Juni 2016 / Magn Reson Med 16-channel bow tie antenna transceiver array for cardiac MR at 7.0 Tesla C. Oezerdem L. Winter A. Graessl K. Paul A. Els O. Weinberger J. Rieger A. Kuehne M. Dieringer F. Hezel D. Voit J. Frahm T. Niendorf 01. April 2016 / Arch Med Sci Mutations in NEBL encoding the cardiac Z-disk protein nebulette are associated with various cardiomyopathies A. Perrot P. Tomasov E. Villard R. Faludi P. Melacini J. Lossie N. Lohmann P. Richard M. De Bortoli A. Angelini A. Varga-Szemes S.R. Sperling T. Simor J. Veselka C. Oezcelik P. Charron Seitennummerierung Aktuelle Seite 1 Seite 2 Nächste Seite Next › Letzte Seite Last »
01. Januar 2016 Human genetics of ventricular septal defect K. Bellmann A. Perrot S. Rickert-Sperling
01. Januar 2016 Congenital heart diseases: the broken heart : clinical features, human genetics and molecular pathways S. Rickert-Sperling R.G. Kelly D.J. Driscoll
01. Januar 2016 Cardiac transcription factors and regulatory networks M. Grunert C. Dorn S. Rickert-Sperling
01. Januar 2016 Human genetics of tetralogy of fallot and double outlet right ventricle C. Dorn A. Perrot S. Rickert-Sperling
01. Januar 2016 Technologies to study genetics and molecular pathways C. Dorn M. Grunert A. Dopazo F. Sanchez-Cabo A. Gatto J. Vazquez S. Rickert-Sperling E. Lara-Pezzi
01. Februar 2016 / Cardiovasc Res Congenital coronary artery anomalies: a bridge from embryology to anatomy and pathophysiology-a position statement of the development, anatomy, and pathology ESC Working Group J.M. Perez-Pomares J.L. de la Pompa D. Franco D. Henderson S.Y. Ho L. Houyel R.G. Kelly D. Sedmera M. Sheppard S. Sperling G. Thiene M. van den Hoff C. Basso
01. Juni 2016 / Magn Reson Med 16-channel bow tie antenna transceiver array for cardiac MR at 7.0 Tesla C. Oezerdem L. Winter A. Graessl K. Paul A. Els O. Weinberger J. Rieger A. Kuehne M. Dieringer F. Hezel D. Voit J. Frahm T. Niendorf
01. April 2016 / Arch Med Sci Mutations in NEBL encoding the cardiac Z-disk protein nebulette are associated with various cardiomyopathies A. Perrot P. Tomasov E. Villard R. Faludi P. Melacini J. Lossie N. Lohmann P. Richard M. De Bortoli A. Angelini A. Varga-Szemes S.R. Sperling T. Simor J. Veselka C. Oezcelik P. Charron