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Year Number of Results
2000 1
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127 results

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Page 1
Tetralogy of Fallot.
Apitz C, Webb GD, Redington AN. Apitz C, et al. Lancet. 2009 Oct 24;374(9699):1462-71. doi: 10.1016/S0140-6736(09)60657-7. Epub 2009 Aug 14. Lancet. 2009. PMID: 19683809 Free article. Review.
2019 updated consensus statement on the diagnosis and treatment of pediatric pulmonary hypertension: The European Pediatric Pulmonary Vascular Disease Network (EPPVDN), endorsed by AEPC, ESPR and ISHLT.
Hansmann G, Koestenberger M, Alastalo TP, Apitz C, Austin ED, Bonnet D, Budts W, D'Alto M, Gatzoulis MA, Hasan BS, Kozlik-Feldmann R, Kumar RK, Lammers AE, Latus H, Michel-Behnke I, Miera O, Morrell NW, Pieles G, Quandt D, Sallmon H, Schranz D, Tran-Lundmark K, Tulloh RMR, Warnecke G, Wåhlander H, Weber SC, Zartner P. Hansmann G, et al. Among authors: apitz c. J Heart Lung Transplant. 2019 Sep;38(9):879-901. doi: 10.1016/j.healun.2019.06.022. Epub 2019 Jun 21. J Heart Lung Transplant. 2019. PMID: 31495407
Pediatric pulmonary hypertension.
Apitz C, Lammers AE. Apitz C, et al. Cardiovasc Diagn Ther. 2021 Aug;11(4):1023-1027. doi: 10.21037/cdt-21-156. Cardiovasc Diagn Ther. 2021. PMID: 34527527 Free PMC article. No abstract available.
Treatment of pulmonary arterial hypertension in children.
Latus H, Delhaas T, Schranz D, Apitz C. Latus H, et al. Among authors: apitz c. Nat Rev Cardiol. 2015 Apr;12(4):244-54. doi: 10.1038/nrcardio.2015.6. Epub 2015 Feb 3. Nat Rev Cardiol. 2015. PMID: 25645500 Review.
Pulmonary hypertension in adults with congenital heart defects (ACHDs) in light of the 2022 ESC PAH guidelines-part II: supportive therapy, special situations (pregnancy, contraception, non-cardiac surgery), targeted pharmacotherapy, organ transplantation, special management (shunt lesion, left ventricular disease, univentricular hearts), interventions, intensive care, ACHD follow-up, future perspective.
Kaemmerer H, Diller GP, Dähnert I, Achenbach S, Eichstaedt CA, Eicken A, Freiberger A, Freilinger S, Geiger R, Gorenflo M, Grünig E, Hager A, Huntgeburth M, Kaemmerer-Suleiman AS, Kozlik-Feldmann R, Lammers AE, Nagdyman N, Michel S, Schmidt KH, Suleiman M, Uebing A, von Scheidt F, Herberg U, Apitz C. Kaemmerer H, et al. Among authors: apitz c. Cardiovasc Diagn Ther. 2024 Oct 31;14(5):921-934. doi: 10.21037/cdt-24-167. Epub 2024 Oct 22. Cardiovasc Diagn Ther. 2024. PMID: 39513142 Free PMC article. Review.
De novo variants in RNF213 are associated with a clinical spectrum ranging from Leigh syndrome to early-onset stroke.
Brunet T, Zott B, Lieftüchter V, Lenz D, Schmidt A, Peters P, Kopajtich R, Zaddach M, Zimmermann H, Hüning I, Ballhausen D, Staufner C, Bianzano A, Hughes J, Taylor RW, McFarland R, Devlin A, Mihaljević M, Barišić N, Rohlfs M, Wilfling S, Sondheimer N, Hewson S, Marinakis NM, Kosma K, Traeger-Synodinos J, Elbracht M, Begemann M, Trepels-Kottek S, Hasan D, Scala M, Capra V, Zara F, van der Ven AT, Driemeyer J, Apitz C, Krämer J, Strong A, Hakonarson H, Watson D, Mayr JA, Prokisch H, Meitinger T, Borggraefe I, Spiegler J, Baric I, Paolini M, Gerstl L, Wagner M. Brunet T, et al. Among authors: apitz c. Genet Med. 2024 Feb;26(2):101013. doi: 10.1016/j.gim.2023.101013. Epub 2023 Nov 1. Genet Med. 2024. PMID: 37924258 Free article.
Pathogenic SMAD6 variants in patients with idiopathic and complex congenital heart disease associated pulmonary arterial hypertension.
Karl S, Grünig E, Shaukat M, Held M, Apitz C, von Scheidt F, Geiger R, Halank M, Olsson KM, Hoeper MM, Kamp JC, Kovacs G, Olschewski H, Seyfarth HJ, Milger K, Ewert R, Klose H, Egenlauf B, Xanthouli P, Hinderhofer K, Eichstaedt CA. Karl S, et al. Among authors: apitz c. NPJ Genom Med. 2025 Mar 25;10(1):28. doi: 10.1038/s41525-025-00484-6. NPJ Genom Med. 2025. PMID: 40133303 Free PMC article.
127 results