Dysfunctional pulmonary artery conduit and co-existing large pseudoaneurysm: well-suited for a percutaneous approach with the Melody valve?

por Kubicki, Rouven, Stiller, Brigitte, Grohmann, Jochen
Publicado 2016

A Rare Case of Severe Dilated Cardiomyopathy in Early Infancy

por Schwendt, Meike, Kroll, Johannes, Fleck, Thilo, Stiller, Brigitte
Publicado 2021

Left recurrent laryngeal nerve palsy following aortic arch stenting: A case report

por Fürniss, Hannah Elisabeth, Hummel, Johanna, Stiller, Brigitte, Grohmann, Jochen
Publicado 2019

Nitric oxide synthases in infants and children with pulmonary hypertension and congenital heart disease

por Hoehn, Thomas, Stiller, Brigitte, McPhaden, Allan R, Wadsworth, Roger M
Publicado 2009

Catheter strategy to ease the procedure and reduce radiation exposure when requiring neck access

por Kubicki, Rouven, Hummel, Johanna, Höhn, René, Müller, Kevin, Stiller, Brigitte, Grohmann, Jochen
Publicado 2020

Retrograde transcatheter aortic valve closure in an infant with failing Norwood stage I palliation: a case report

por Fürniss, Hannah E., Kubicki, Rouven, Stiller, Brigitte, Reineker, Katja, Siepe, Matthias, Grohmann, Jochen
Publicado 2019

Dysphagia after arteria lusoria dextra surgery: Anatomical considerations before redo-surgery

por Mayer, Judith, van der Werf-Grohmann, Natascha, Kroll, Johannes, Spiekerkoetter, Ute, Stiller, Brigitte, Grohmann, Jochen
Publicado 2017

Fascicular parasystole and recurrent syncope – a case report

por Steinfurt, Johannes, Asbach, Stefan, Odening, Katja E, Faber, Thomas S, Stiller, Brigitte, Bode, Christoph, Biermann, Jürgen
Publicado 2018

Longitudinal Evaluation of Aortic Hemodynamics in Marfan Syndrome: New Insights from a 4D Flow Cardiovascular Magnetic Resonance Multi-Year Follow-Up Study

por Geiger, Julia, Hirtler, Daniel, Gottfried, Kristina, Rahman, Ozair, Bollache, Emilie, Barker, Alex J., Markl, Michael, Stiller, Brigitte
Publicado 2017

Risk Assessment of Red Cell Transfusion in Congenital Heart Disease

por Zürn, Christoph, Höhn, René, Hübner, David, Umhau, Markus, Kroll, Johannes, Kari, Fabian A., Humburger, Frank, Maier, Sven, Stiller, Brigitte
Publicado 2022

Primary carnitine deficiency – diagnosis after heart transplantation: better late than never!

por Grünert, Sarah C., Tucci, Sara, Schumann, Anke, Schwendt, Meike, Gramer, Gwendolyn, Hoffmann, Georg F., Erbel, Michelle, Stiller, Brigitte, Spiekerkoetter, Ute
Publicado 2020

A Homozygous Deletion of Exon 5 of KYNU Resulting from a Maternal Chromosome 2 Isodisomy (UPD2) Causes Catel-Manzke-Syndrome/VCRL Syndrome

por Schüle, Isabel, Berger, Urs, Matysiak, Uta, Ruzaike, Gunda, Stiller, Brigitte, Pohl, Martin, Spiekerkoetter, Ute, Lausch, Ekkehart, Grünert, Sarah C., Schmidts, Miriam
Publicado 2021

Quantitative collagen assessment in right ventricular myectomies from patients with tetralogy of Fallot

por Wülfers, Eike M, Greiner, Joachim, Giese, Max, Madl, Josef, Kroll, Johannes, Stiller, Brigitte, Kohl, Peter, Rog-Zielinska, Eva A, Fürniss, Hannah E
Publicado 2021

Model-driven survival prediction after congenital heart surgery

por Zürn, Christoph, Hübner, David, Ziesenitz, Victoria C, Höhn, René, Schuler, Lena, Schlange, Tim, Gorenflo, Matthias, Kari, Fabian A, Kroll, Johannes, Loukanov, Tsvetomir, Klemm, Rolf, Stiller, Brigitte
Publicado 2023

Long-term safety and tolerability of valsartan in children aged 6 to 17 years with hypertension

por Lou-Meda, Randall, Stiller, Brigitte, Antonio, Zenaida L., Zielinska, Ewa, Yap, Hui-Kim, Kang, Hee Gyung, Tan, Monique, Glazer, Robert D., Valentin, Michele A., Wang, Linda
Publicado 2018

A gain-of-function TBX20 mutation causes congenital atrial septal defects, patent foramen ovale and cardiac valve defects

por Posch, Maximilian G, Gramlich, Michael, Sunde, Margaret, Schmitt, Katharina R, Lee, Stella H Y, Richter, Silke, Kersten, Andrea, Perrot, Andreas, Panek, Anna N, Al Khatib, Iman H, Nemer, Georges, Mégarbané, André, Dietz, Rainer, Stiller, Brigitte, Berger, Felix, Harvey, Richard P, Özcelik, Cemil
Publicado 2010

Effect and safety of treatment with ACE-inhibitor Enalapril and β-blocker metoprolol on the onset of left ventricular dysfunction in Duchenne muscular dystrophy - a randomized, dou...

por Dittrich, Sven, Graf, Erika, Trollmann, Regina, Neudorf, Ulrich, Schara, Ulrike, Heilmann, Antje, von der Hagen, Maja, Stiller, Brigitte, Kirschner, Janbernd, Pozza, Robert Dalla, Müller-Felber, Wolfgang, Weiss, Katja, von Au, Katja, Khalil, Markus, Motz, Reinald, Korenke, Christoph, Lange, Martina, Wilichowski, Ekkehard, Pattathu, Joseph, Ebinger, Friedrich, Wiechmann, Nicola, Schröder, Rolf
Publicado 2019

Adrenergic Repression of the Epigenetic Reader MeCP2 Facilitates Cardiac Adaptation in Chronic Heart Failure

por Mayer, Sandra C., Gilsbach, Ralf, Preissl, Sebastian, Monroy Ordonez, Elsa Beatriz, Schnick, Tilman, Beetz, Nadine, Lother, Achim, Rommel, Carolin, Ihle, Hannah, Bugger, Heiko, Rühle, Frank, Schrepper, Andrea, Schwarzer, Michael, Heilmann, Claudia, Bönisch, Ulrike, Gupta, Shashi Kumar, Wilpert, Jochen, Kretz, Oliver, von Elverfeldt, Dominik, Orth, Joachim, Aktories, Klaus, Beyersdorf, Friedhelm, Bode, Christoph, Stiller, Brigitte, Krüger, Markus, Thum, Thomas, Doenst, Torsten, Stoll, Monika, Hein, Lutz
Publicado 2015

Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease

por Audain, Enrique, Wilsdon, Anna, Breckpot, Jeroen, Izarzugaza, Jose M. G., Fitzgerald, Tomas W., Kahlert, Anne-Karin, Sifrim, Alejandro, Wünnemann, Florian, Perez-Riverol, Yasset, Abdul-Khaliq, Hashim, Bak, Mads, Bassett, Anne S., Benson, Woodrow D., Berger, Felix, Daehnert, Ingo, Devriendt, Koenraad, Dittrich, Sven, Daubeney, Piers EF, Garg, Vidu, Hackmann, Karl, Hoff, Kirstin, Hofmann, Philipp, Dombrowsky, Gregor, Pickardt, Thomas, Bauer, Ulrike, Keavney, Bernard D., Klaassen, Sabine, Kramer, Hans-Heiner, Marshall, Christian R., Milewicz, Dianna M., Lemaire, Scott, Coselli, Joseph S., Mitchell, Michael E., Tomita-Mitchell, Aoy, Prakash, Siddharth K., Stamm, Karl, Stewart, Alexandre F. R., Silversides, Candice K., Siebert, Reiner, Stiller, Brigitte, Rosenfeld, Jill A., Vater, Inga, Postma, Alex V., Caliebe, Almuth, Brook, J. David, Andelfinger, Gregor, Hurles, Matthew E., Thienpont, Bernard, Larsen, Lars Allan, Hitz, Marc-Phillip
Publicado 2021

Correction: Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease

por Audain, Enrique, Wilsdon, Anna, Breckpot, Jeroen, Izarzugaza, Jose M. G., Fitzgerald, Tomas W., Kahlert, Anne-Karin, Sifrim, Alejandro, Wünnemann, Florian, Perez-Riverol, Yasset, Abdul-Khaliq, Hashim, Bak, Mads, Bassett, Anne S., Benson, D. Woodrow, Berger, Felix, Daehnert, Ingo, Devriendt, Koenraad, Dittrich, Sven, Daubeney, Piers EF, Garg, Vidu, Hackmann, Karl, Hoff, Kirstin, Hofmann, Philipp, Dombrowsky, Gregor, Pickardt, Thomas, Bauer, Ulrike, Keavney, Bernard D., Klaassen, Sabine, Kramer, Hans-Heiner, Marshall, Christian R., Milewicz, Dianna M., Lemaire, Scott, Coselli, Joseph S., Mitchell, Michael E., Tomita-Mitchell, Aoy, Prakash, Siddharth K., Stamm, Karl, Stewart, Alexandre F. R., Silversides, Candice K., Siebert, Reiner, Stiller, Brigitte, Rosenfeld, Jill A., Vater, Inga, Postma, Alex V., Caliebe, Almuth, Brook, J. David, Andelfinger, Gregor, Hurles, Matthew E., Thienpont, Bernard, Larsen, Lars Allan, Hitz, Marc-Phillip
Publicado 2021