Long-term early development research in congenital heart disease (LEADER-CHD): a study protocol for a prospective cohort observational study investigating the development of childr...

por Ferentzi, Hannah, Pfitzer, Constanze, Rosenthal, Lisa-Maria, Berger, Felix, Schmitt, Katharina R L
Publicado 2017

Combined Cyclosporin A and Hypothermia Treatment Inhibits Activation of BV-2 Microglia but Induces an Inflammatory Response in an Ischemia/Reperfusion Hippocampal Slice Culture Mod...

por Wowro, Sylvia J., Tong, Giang, Krech, Jana, Rolfs, Nele, Berger, Felix, Schmitt, Katharina R. L.
Publicado 2019

Cooling and Sterile Inflammation in an Oxygen-Glucose-Deprivation/Reperfusion Injury Model in BV-2 Microglia

por Lücht, Jana, Rolfs, Nele, Wowro, Sylvia J., Berger, Felix, Schmitt, Katharina R. L., Tong, Giang
Publicado 2021

Post-TTM Rebound Pyrexia after Ischemia-Reperfusion Injury Results in Sterile Inflammation and Apoptosis in Cardiomyocytes

por Tong, Giang, von Garlen, Nalina N. A., Wowro, Sylvia J., Lam, Phuong D., Krech, Jana, Berger, Felix, Schmitt, Katharina R. L.
Publicado 2019

New Insights into the Education of Children with Congenital Heart Disease with and without Trisomy 21

por Schmitt, Katharina R. L., Sievers, Laura K., Hütter, Alina, Abdul-Khaliq, Hashim, Poryo, Martin, Berger, Felix, Bauer, Ulrike M. M., Helm, Paul C., Pfitzer, Constanze
Publicado 2023

Microcephaly is associated with impaired educational development in children with congenital heart disease

por Pfitzer, Constanze, Sievers, Laura K., Hütter, Alina, Khaliq, Hashim-Abdul, Poryo, Martin, Berger, Felix, Bauer, Ulrike M. M., Helm, Paul C., Schmitt, Katharina R. L.
Publicado 2022

The German EMPATHIC-30 Questionnaire Showed Reliability and Convergent Validity for Use in an Intermediary/General Pediatric Cardiology Unit: A Psychometric Evaluation

por Girch, Alona, Rippe, Ralph C. A., Latour, Jos M., Jönebratt Stocker, Michaela, Blendermann, Magdalena, Hoffmann, Katharina, Heppner, Hannes, Berger, Felix, Schmitt, Katharina R. L., Ferentzi, Hannah
Publicado 2022

Family-Centered Care at Pediatric Cardiac Intensive Care Units in Germany and the Relationship With Parent and Infant Well-Being: A Study Protocol

por Ferentzi, Hannah, Rippe, Ralph C. A., Latour, Jos M., Schubert, Stephan, Girch, Alona, Jönebratt Stocker, Michaela, Pfitzer, Constanze, Photiadis, Joachim, Sandica, Eugen, Berger, Felix, Schmitt, Katharina R. L.
Publicado 2021

Cardiac Alpha-Myosin (MYH6) Is the Predominant Sarcomeric Disease Gene for Familial Atrial Septal Defects

por Posch, Maximilian G., Waldmuller, Stephan, Müller, Melanie, Scheffold, Thomas, Fournier, David, Andrade-Navarro, Miguel A., De Geeter, Bernard, Guillaumont, Sophie, Dauphin, Claire, Yousseff, Dany, Schmitt, Katharina R., Perrot, Andreas, Berger, Felix, Hetzer, Roland, Bouvagnet, Patrice, Özcelik, Cemil
Publicado 2011

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