Molecular Mechanisms of Inherited Arrhythmias

por Wolf, Cordula M, Berul, Charles I
Publicado 2008

Compound Mutation in Cardiac Sarcomere Proteins Is Associated with Increased Risk for Major Arrhythmic Events in Pediatric Onset Hypertrophic Cardiomyopathy

por Pollmann, Kathrin, Kaltenecker, Emanuel, Schleihauf, Julia, Ewert, Peter, Görlach, Agnes, Wolf, Cordula M.
Publicado 2021

Reclassification of genetic variants in children with long QT syndrome

por Westphal, Dominik S., Burkard, Tobias, Moscu‐Gregor, Alexander, Gebauer, Roman, Hessling, Gabriele, Wolf, Cordula M.
Publicado 2020

NADPH oxidases and HIF1 promote cardiac dysfunction and pulmonary hypertension in response to glucocorticoid excess

por Kračun, Damir, Klop, Mathieu, Knirsch, Anna, Petry, Andreas, Kanchev, Ivan, Chalupsky, Karel, Wolf, Cordula M., Görlach, Agnes
Publicado 2020

Fetal Bradycardia Caused by Monogenic Disorders—A Review of the Literature

por Westphal, Dominik S., Hauser, Michael, Beckmann, Britt-Maria, Wolf, Cordula M., Hessling, Gabriele, Oberhoffer-Fritz, Renate, Wacker-Gussmann, Annette
Publicado 2022

Peak Oxygen Uptake on Cardiopulmonary Exercise Test Is a Predictor for Severe Arrhythmic Events during Three-Year Follow-Up in Patients with Complex Congenital Heart Disease

por von Sanden, Felix, Ptushkina, Svetlana, Hock, Julia, Fritz, Celina, Hörer, Jürgen, Hessling, Gabriele, Ewert, Peter, Hager, Alfred, Wolf, Cordula M.
Publicado 2022

Cytoplasmic CUG RNA Foci Are Insufficient to Elicit Key DM1 Features

por Dansithong, Warunee, Wolf, Cordula M., Sarkar, Partha, Paul, Sharan, Chiang, Andy, Holt, Ian, Morris, Glenn E., Branco, Dorothy, Sherwood, Megan C., Comai, Lucio, Berul, Charles I., Reddy, Sita
Publicado 2008

EGFR and MMP-9 are associated with neointimal hyperplasia in systemic-to-pulmonary shunts in children with complex cyanotic heart disease

por Kottmann, Philip, Eildermann, Katja, Murthi, Sarala Raj, Cleuziou, Julie, Lemmer, Julia, Vitanova, Keti, von Stumm, Maria, Lehmann, Luisa, Hörer, Jürgen, Ewert, Peter, Sigler, Matthias, Lange, Rüdiger, Lahm, Harald, Dreßen, Martina, Lichtner, Peter, Wolf, Cordula M.
Publicado 2023

Cell cycle defects underlie childhood-onset cardiomyopathy associated with Noonan syndrome

por Meier, Anna B., Raj Murthi, Sarala, Rawat, Hilansi, Toepfer, Christopher N., Santamaria, Gianluca, Schmid, Manuel, Mastantuono, Elisa, Schwarzmayr, Thomas, Berutti, Riccardo, Cleuziou, Julie, Ewert, Peter, Görlach, Agnes, Klingel, Karin, Laugwitz, Karl-Ludwig, Seidman, Christine E., Seidman, Jonathan G., Moretti, Alessandra, Wolf, Cordula M.
Publicado 2021

Clinical presentation of calmodulin mutations: the International Calmodulinopathy Registry

por Crotti, Lia, Spazzolini, Carla, Nyegaard, Mette, Overgaard, Michael T, Kotta, Maria-Christina, Dagradi, Federica, Sala, Luca, Aiba, Takeshi, Ayers, Mark D, Baban, Anwar, Barc, Julien, Beach, Cheyenne M, Behr, Elijah R, Bos, J Martijn, Cerrone, Marina, Covi, Peter, Cuneo, Bettina, Denjoy, Isabelle, Donner, Birgit, Elbert, Adrienne, Eliasson, Håkan, Etheridge, Susan P, Fukuyama, Megumi, Girolami, Francesca, Hamilton, Robert, Horie, Minoru, Iascone, Maria, Jaimez, Juan Jiménez, Jensen, Henrik Kjærulf, Kannankeril, Prince J, Kaski, Juan P, Makita, Naomasa, Muñoz-Esparza, Carmen, Odland, Hans H, Ohno, Seiko, Papagiannis, John, Porretta, Alessandra Pia, Prandstetter, Christopher, Probst, Vincent, Robyns, Tomas, Rosenthal, Eric, Rosés-Noguer, Ferran, Sekarski, Nicole, Singh, Anoop, Spentzou, Georgia, Stute, Fridrike, Tfelt-Hansen, Jacob, Till, Jan, Tobert, Kathryn E, Vinocur, Jeffrey M, Webster, Gregory, Wilde, Arthur A M, Wolf, Cordula M, Ackerman, Michael J, Schwartz, Peter J
Publicado 2023