Oechslin, Erwin

ESC Guidelines for the management of grown-up congenital heart disease (new version 2010)

Endorsed by the Association for European Paediatric Cardiology (AEPC), Authors/Task Force Members, Baumgartner, H., Bonhoeffer, P., De Groot, N. M. S., de Haan, F., Deanfield, J. E., Galie, N., Gatzoulis, M. A., Gohlke-Baerwolf, C., et al. (2010) · European Heart Journal

Congenital Heart Disease StudiesCardiovascular and Diving-Related Complications

Cited by 2,331

The spectrum of adult congenital heart disease in Europe: morbidity and mortality in a 5 year follow-up period

Engelfriet, P., Boersma, E., Oechslin, E., Tijssen, J., Gatzoulis, M. A., Thilén, U., Kaemmerer, H., Moons, P., Meijboom, F., Popelová, J., et al. (2005) · European Heart Journal

Congenital Heart Disease StudiesCardiovascular and Diving-Related Complications

Cited by 413

Sudden cardiac death in adult congenital heart disease

Koyak, Z., Harris, L., de Groot, J. R., Silversides, C. K., Oechslin, E. N., Bouma, B. J., Budts, W., Zwinderman, A. H., Van Gelder, I. C., & Mulder, B. J. M. (2012) · Circulation

Congenital Heart Disease StudiesCardiac electrophysiology and arrhythmias

Cited by 378

Reoperation in adults with repair of tetralogy of Fallot: indications and outcomes.

Oechslin, E. N., Harrison, D. A., Harris, L., Downar, E., Webb, G. D., Siu, S. S., & Williams, W. G. (1999) · The Journal of Thoracic and Cardiovascular Surgery

Congenital Heart Disease StudiesCongenital heart defects research

Cited by 264

Haploinsufficiency of vascular endothelial growth factor related signaling genes is associated with tetralogy of Fallot

Reuter, M. S., Jobling, R., Chaturvedi, R. R., Manshaei, R., Costain, G., Heung, T., Curtis, M., Hosseini, S. M., Liston, E., Lowther, C., et al. (2019) · Genetics in Medicine

Congenital Heart Disease StudiesCongenital heart defects research

Cited by 85

Genes and pathways implicated in tetralogy of Fallot revealed by ultra-rare variant burden analysis in 231 genome sequences

Manshaei, R., Merico, D., Reuter, M. S., Engchuan, W., Mojarad, B. A., Chaturvedi, R., Heung, T., Pellecchia, G., Zarrei, M., Nalpathamkalam, T., et al. (2020) · Frontiers in Genetics

Genomics and Rare DiseasesCongenital heart defects research

Cited by 36