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Utility of deep learning networks for the generation of artificial cardiac magnetic resonance images in congenital heart disease.
Diller GP, Vahle J, Radke R, Vidal MLB, Fischer AJ, Bauer UMM, Sarikouch S, Berger F, Beerbaum P, Baumgartner H, Orwat S; German Competence Network for Congenital Heart Defects Investigators. Diller GP, et al. Among authors: berger f. BMC Med Imaging. 2020 Oct 8;20(1):113. doi: 10.1186/s12880-020-00511-1. BMC Med Imaging. 2020. PMID: 33032536 Free PMC article.
Integrated analysis of atrioventricular interactions in tetralogy of Fallot.
Riesenkampff E, Mengelkamp L, Mueller M, Kropf S, Abdul-Khaliq H, Sarikouch S, Beerbaum P, Hetzer R, Steendijk P, Berger F, Kuehne T. Riesenkampff E, et al. Among authors: berger f. Am J Physiol Heart Circ Physiol. 2010 Aug;299(2):H364-71. doi: 10.1152/ajpheart.00264.2010. Epub 2010 May 21. Am J Physiol Heart Circ Physiol. 2010. PMID: 20495149 Free PMC article.
T1 mapping in ischaemic heart disease.
h-Ici DO, Jeuthe S, Al-Wakeel N, Berger F, Kuehne T, Kozerke S, Messroghli DR. h-Ici DO, et al. Among authors: berger f. Eur Heart J Cardiovasc Imaging. 2014 Jun;15(6):597-602. doi: 10.1093/ehjci/jeu024. Epub 2014 Feb 23. Eur Heart J Cardiovasc Imaging. 2014. PMID: 24566951 Free article. Review.
Current therapy and outcome of Eisenmenger syndrome: data of the German National Register for congenital heart defects.
Diller GP, Körten MA, Bauer UM, Miera O, Tutarel O, Kaemmerer H, Berger F, Baumgartner H; German Competence Network for Congenital Heart Defects Investigators. Diller GP, et al. Among authors: berger f. Eur Heart J. 2016 May 7;37(18):1449-55. doi: 10.1093/eurheartj/ehv743. Epub 2016 Feb 2. Eur Heart J. 2016. PMID: 26843280 Free PMC article.
Frequency of Miscarriage/Stillbirth and Terminations of Pregnancy Among Women With Congenital Heart Disease in Germany, Hungary and Japan.
Koerten MA, Niwa K, Szatmári A, Hajnalka B, Ruzsa Z, Nagdyman N, Niggemeyer E, Peters B, Schneider KT, Kuschel B, Mizuno Y, Berger F, Kaemmerer H, Bauer UM. Koerten MA, et al. Among authors: berger f. Circ J. 2016 Jul 25;80(8):1846-51. doi: 10.1253/circj.CJ-15-1296. Epub 2016 Jun 21. Circ J. 2016. PMID: 27334027 Free article. Clinical Trial.
Distinct genetic architectures for syndromic and nonsyndromic congenital heart defects identified by exome sequencing.
Sifrim A, Hitz MP, Wilsdon A, Breckpot J, Turki SH, Thienpont B, McRae J, Fitzgerald TW, Singh T, Swaminathan GJ, Prigmore E, Rajan D, Abdul-Khaliq H, Banka S, Bauer UM, Bentham J, Berger F, Bhattacharya S, Bu'Lock F, Canham N, Colgiu IG, Cosgrove C, Cox H, Daehnert I, Daly A, Danesh J, Fryer A, Gewillig M, Hobson E, Hoff K, Homfray T; INTERVAL Study; Kahlert AK, Ketley A, Kramer HH, Lachlan K, Lampe AK, Louw JJ, Manickara AK, Manase D, McCarthy KP, Metcalfe K, Moore C, Newbury-Ecob R, Omer SO, Ouwehand WH, Park SM, Parker MJ, Pickardt T, Pollard MO, Robert L, Roberts DJ, Sambrook J, Setchfield K, Stiller B, Thornborough C, Toka O, Watkins H, Williams D, Wright M, Mital S, Daubeney PE, Keavney B, Goodship J; UK10K Consortium; Abu-Sulaiman RM, Klaassen S, Wright CF, Firth HV, Barrett JC, Devriendt K, FitzPatrick DR, Brook JD; Deciphering Developmental Disorders Study; Hurles ME. Sifrim A, et al. Among authors: berger f. Nat Genet. 2016 Sep;48(9):1060-5. doi: 10.1038/ng.3627. Epub 2016 Aug 1. Nat Genet. 2016. PMID: 27479907 Free PMC article.
1,848 results