Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Regina Pribe‐Wolferts"'
Autor:
Mustafa Yildirim, Christoph Reich, Christian Salbach, Regina Pribe‐Wolferts, Barbara Ruth Milles, Tobias Täger, Matthias Mueller‐Hennessen, Markus Weiler, Benjamin Meder, Norbert Frey, Evangelos Giannitsis
Publikováno v:
ESC Heart Failure, Vol 11, Iss 6, Pp 3732-3741 (2024)
Abstract Aims Concentrations of high‐sensitivity cardiac troponin T (hs‐cTnT) are frequently elevated in stable patients with confirmed muscle dystrophies. However, sparse information is available on the interpretation of serial concentration cha
Externí odkaz:
https://doaj.org/article/edafe5ea1c43436b9d9fd5c4d91a2a6f
Autor:
Ruxandra Jurcut, Andrea Ros, Luisa Politano, Juan Jiménez-Jáimez, Pablo García-Pavía, Ali Yilmaz, Job A J Verdonschot, Alberto Palladino, María I. García-Álvarez, Luis Ruiz-Guerrero, Karim Wahbi, Ana García-Álvarez, Luis R. Lopes, Michael Arad, Maria Teresa Basurte Elorz, Jens Mogensen, Roberto Barriales-Villa, Paloma Jordà, José M. Larrañaga-Moreira, Francisco Bermúdez-Jiménez, Zofia T. Bilińska, Benjamin Meder, Rosa L. E. van Loon, Zornitsa Shomanova, Tanya Stojkovic, Francesca Girolami, Miloš Kubánek, Julián Palomino-Doza, Perry M. Elliott, Torsten Bloch Rasmussen, Dov Freimark, Maria Robledo Iñarritu, María Alejandra Restrepo-Córdoba, Giovanni Quarta, Pascal Laforêt, Anca Florian, Juan Pablo Ochoa, Regina Pribe-Wolferts, Ramon Brugada, Rasmus B Hansen, Vicente Climent-Payá, Fernando Domínguez, José Rodríguez-Palomares
Publikováno v:
European journal of heart failure, 23(8), 1276-1286. Wiley
DDFV. Repositorio Institucional de la Universidad Francisco de Vitoria
instname
Restrepo-Cordoba, M A, Wahbi, K, Florian, A R, Jiménez-Jáimez, J, Politano, L, Arad, M, Climent-Paya, V, Garcia-Alvarez, A, Hansen, R B, Larrañaga-Moreira, J M, Kubanek, M, Lopes, L R, Ros, A, Jurcut, R, Rasmussen, T B, Ruiz-Guerrero, L, Pribe-Wolferts, R, Palomino-Doza, J, Bilinska, Z, Rodríguez-Palomares, J F, Van Loon, R L E, Basurte Elorz, M T, Quarta, G, Robledo Iñarritu, M, Verdonschot, J A J, Stojkovic, T, Shomanova, Z, Bermudez-Jimenez, F, Palladino, A, Freimark, D, García-Álvarez, M I, Jorda, P, Dominguez, F, Ochoa, J P, Girolami, F, Brugada, R, Meder, B, Barriales-Villa, R, Mogensen, J, Laforêt, P, Yilmaz, A, Elliott, P, Garcia-Pavia, P & for the European Genetic Cardiomyopathies Initiative Investigators (see online supplementary Appendix S1) 2021, ' Prevalence and clinical outcomes of dystrophin-associated dilated cardiomyopathy without severe skeletal myopathy ', European Journal of Heart Failure, vol. 23, no. 8, pp. 1276-1286 . https://doi.org/10.1002/ejhf.2250
DDFV. Repositorio Institucional de la Universidad Francisco de Vitoria
instname
Restrepo-Cordoba, M A, Wahbi, K, Florian, A R, Jiménez-Jáimez, J, Politano, L, Arad, M, Climent-Paya, V, Garcia-Alvarez, A, Hansen, R B, Larrañaga-Moreira, J M, Kubanek, M, Lopes, L R, Ros, A, Jurcut, R, Rasmussen, T B, Ruiz-Guerrero, L, Pribe-Wolferts, R, Palomino-Doza, J, Bilinska, Z, Rodríguez-Palomares, J F, Van Loon, R L E, Basurte Elorz, M T, Quarta, G, Robledo Iñarritu, M, Verdonschot, J A J, Stojkovic, T, Shomanova, Z, Bermudez-Jimenez, F, Palladino, A, Freimark, D, García-Álvarez, M I, Jorda, P, Dominguez, F, Ochoa, J P, Girolami, F, Brugada, R, Meder, B, Barriales-Villa, R, Mogensen, J, Laforêt, P, Yilmaz, A, Elliott, P, Garcia-Pavia, P & for the European Genetic Cardiomyopathies Initiative Investigators (see online supplementary Appendix S1) 2021, ' Prevalence and clinical outcomes of dystrophin-associated dilated cardiomyopathy without severe skeletal myopathy ', European Journal of Heart Failure, vol. 23, no. 8, pp. 1276-1286 . https://doi.org/10.1002/ejhf.2250
Aims: Dilated cardiomyopathy (DCM) associated with dystrophin gene (DMD) mutations in individuals with mild or absent skeletal myopathy is often indistinguishable from other DCM forms. We sought to describe the phenotype and prognosis of DMD associat
Autor:
Huan Lan, Daniel Nowak, Hugo A. Katus, Zhihan Zhao, Martin Borggrefe, Xiaobo Zhou, Dierk Thomas, Siegfried Lang, Thomas Wieland, Katherine Sattler, Xin Li, Gökhan Yücel, Kleopatra Rapti, Karen Bieback, Antonius Ratte, Lukas Cyganek, Regina Pribe-Wolferts, Ursula Ravens, Patrick Most, Ibrahim Akin, Wolfram-Hubertus Zimmermann, Janina Wittig, Oliver Müller, Constanze Schmidt, Ibrahim El-Battrawy, Jochen Utikal, Jan-Dierk Schünemann, Ralf Bauer
Publikováno v:
Circulation: Genomic and Precision Medicine. 11
Background: Limb-Girdle muscular dystrophies (LGMD) are a heritable group of genetically determined disorders with a primary involvement of the pelvic or shoulder girdle musculature with partially cardiac manifestation, such as dilated cardiomyopathy
Autor:
Patrick A. Schweizer, Constanze Merten, Derliz Mereles, Rüdiger Becker, Mohamed A Abdelrazek, Benjamin Meder, Regina Pribe-Wolferts, Dierk Thomas, Florian Andre, Jennifer Franke, Jin Li, Philipp Ehlermann, Hugo A. Katus
Publikováno v:
Clinical Research in Cardiology. 104:241-249
Left ventricular noncompaction (LVNC) is a cardiomyopathy with hypertrabeculation of the LV, often complicated by heart failure, arrhythmia and thromboembolic events. The features of LVNC are still incompletely characterized due to its late recogniti
Autor:
Yuhua Liao, Alan Lai, Christoph Dieterich, Jan Haas, Diana Martins Bordalo, Sabine Haßfeld, Omid Shirvani Samani, Min Wang, Qiutang Zeng, Feng Zhu, Li Yuan, Hugo A. Katus, Min Zhou, Michael Gotthardt, Regina Pribe-Wolferts, Benjamin Meder, Tobias Fehlmann, Ali Amr, Daniel Tian Li, Kai Huang, Ming Nie, Martin Liss, Zihua Zhou, Marion Müller, Katrin Streckfuß-Bömeke, Christine Schwartz, Jing Wang, Elham Kayvanpour, Christian Geier, Andreas Keller, Karen S. Frese, Yan-Wen Shu, Jing Shao, Avisha Carstensen, Philipp Ehlermann, Christine Fischer, Farbod Sedaghat-Hamedani, Long-Xian Cheng
Publikováno v:
European heart journal. 38(46)
Aims: In this study, we aimed to clinically and genetically characterize LVNC patients and investigate the prevalence of variants in known and novel LVNC disease genes. Introduction: Left ventricular non-compaction cardiomyopathy (LVNC) is an increas
Publikováno v:
SpringerReference Innere Medizin ISBN: 9783642546761
DGIM Innere Medizin ISBN: 9783642546761
DGIM Innere Medizin ISBN: 9783642546761
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4469f9fda9b26a9f68f6bfb4ee600fbb
https://doi.org/10.1007/978-3-642-54676-1_185-1
https://doi.org/10.1007/978-3-642-54676-1_185-1
Autor:
Jan Haas, Hugo A. Katus, Benjamin Meder, Christian Geier, Jennifer Franke, Karen S. Frese, Elham Kayvanpour, Andreas Keller, Justo Lorenzo Bermejo, Regina Pribe-Wolferts, Barbara Peil, Farbod Sedaghat-Hamedani, Zhu Feng, Yuhua Liao
Publikováno v:
Circulation. 130
Left ventricular noncompaction cardiomyopathy (LVNC) is an increasingly recognized cause of heart failure, arrhythmias, thrombembolic events, and sudden cardiac death. To better understand the contribution of genetic factors to this disease, allowing
Autor:
Christoph Eisenbach, Wolfgang Stremmel, Hugo A. Katus, Regina Pribe-Wolferts, Felix Lasitschka, Andreas Dösch, Tobias Rehlen
Publikováno v:
Endoscopy. 47:E314-E315