Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Katalin Szöcs"'
Autor:
Betül Toprak, Katalin Szöcs, Elvin Zengin-Sahm, Christoph Sinning, Amra Hot, Peter Bannas, Kurt Hecher, Bernd Hüneke, Thomas S. Mir, Meike Rybczynski, Evaldas Girdauskas, Stefan Blankenberg, Yskert von Kodolitsch
Publikováno v:
Journal of Clinical Medicine, Vol 9, Iss 4, p 1124 (2020)
Pregnancy poses a threat to women with aortopathy. Conclusive data on the obstetric and aortic outcome in this risk collective, especially when it comes to aortic complications in the long term, are still missing. This study offers a comparative anal
Externí odkaz:
https://doaj.org/article/95667b48096d461d89d20ed2cbb33842
Autor:
Yskert von Kodolitsch, Katalin Szöcs, Fachera Ebrahimzada, Guiseppe Panuccio, Fiona Rohlffs, Jens Brickwedel, Christian Detter, E. Sebastian Debus, Tilo Kölbel
Publikováno v:
Gefässchirurgie. 27:302-314
Autor:
Anthony Demolder, Lisa Bianco, Maryanne Caruana, Elena Cervi, Arturo Evangelista, Guillaume Jondeau, Lisa Lauren Buttigieg, Ángela López-Sainz, Elena Montañés Delmás, Alessandro Pini, Anna Sabaté-Rotés, Katalin Szöcs, Maria Tchitchinadze, Gisela Teixidó-Tura, Yskert von Kodolitsch, Laura Muiño-Mosquera, Julie De Backer
Publikováno v:
Scientia
EUROPEAN JOURNAL OF MEDICAL GENETICS
EUROPEAN JOURNAL OF MEDICAL GENETICS
Arrhythmia; Heritable thoracic aortic disease Arritmia; Enfermedad hereditaria de la aorta torácica Arrítmia; Malaltia hereditària de l'aorta toràcica Background Heritable thoracic aortic diseases (HTAD), typically entailing aortic complications,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::800934a2979a9754d52560a4246e2e73
https://hdl.handle.net/11351/8059
https://hdl.handle.net/11351/8059
Autor:
Katalin Szöcs, Betül Toprak, Gerhard Schön, Meike Rybczynski, Tatjana Brinken, Adrian Mahlmann, Evaldas Girdauskas, Stefan Blankenberg, Yskert von Kodolitsch
Publikováno v:
Cardiovascular diagnosis and therapy. 12(4)
Congenital bicuspid aortic valve affects up to 2% of the general population. It occurs in complex congenital heart defects or in syndromes such as Turner, Marfan, or Loeys-Dietz. However, the majority of bicuspid aortic valves are considered to manif
Autor:
Yskert von Kodolitsch, Katalin Szöcs, Christian Detter, Petra Gehle, Tilo Kölbel, Eike Sebastian Debus
Publikováno v:
Klinische Angiologie ISBN: 9783662613795
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c611ade275b1f7d658c7d19fd46c17eb
https://doi.org/10.1007/978-3-662-61379-5_54-1
https://doi.org/10.1007/978-3-662-61379-5_54-1
Autor:
Laura Muiño Mosquera, Anthony Demolder, Katalin Szöcs, Artur Evangelista, Gisela Teixido-Tura, Guillaume Jondeau, A Sabate-Rotes, Elena Cervi, Ángela López-Sainz, Y Von Kodolitsch, Julie De Backer, A Pini, M Caruana, E Montanes-Delmas, L Buttigieg
Publikováno v:
European Heart Journal. 42
Background Marfan syndrome (MFS), Loeys-Dietz syndrome (LDS) and related heritable thoracic aortic diseases (HTAD) are well-known for their aortic complications. Myocardial dysfunction and arrhythmia are less known in this setting but have been incre
Autor:
Julie De Backer, Anji T. Yetman, Nina Riise, Katharina T I Kornhuber, Laura Muiño Mosquera, Katalin Szöcs, Thy Thy Vanem, Ingmar Staufenbiel, Reed E. Pyeritz, Alexander Rahman, Shaine A. Morris, Leema Robert, Enid Neptune, Evaldas Girdauskas, Svend Rand-Hendriksen, Marina Vogler, Stephan J. Linke, Yskert von Kodolitsch, Harald Kaemmerer, Anthony Demolder
Publikováno v:
Expert Review of Cardiovascular Therapy
Introduction: The revised Ghent nosology presents the classical features of Marfan syndrome. However, behind its familiar face, Marfan syndrome hides less well-known features. Areas covered: The German Marfan Organization listed unusual symptoms and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d3f15aa8ba541c1653253a0ae4d15a77
https://biblio.ugent.be/publication/8640129/file/8641526
https://biblio.ugent.be/publication/8640129/file/8641526
Autor:
Harald Kaemmerer, Kerstin Kutsche, Jürgen Berger, Nikolaos Tsilimparis, Julie De Backer, Heide Seidel, Thomas S. Mir, Katalin Szöcs, Alexander M. Bernhardt, Stefan Blankenberg, Laura Muiño Mosquera, Tilo Kölbel, Kristina Mühlstädt, Lauritz Schoof, Yskert von Kodolitsch, Evaldas Girdauskas, Axel Staebler, Jens Brickwedel, Christian Detter, Adrian Mahlmann
Publikováno v:
JOURNAL OF CLINICAL MEDICINE
Journal of Clinical Medicine
Volume 8
Issue 12
Journal of Clinical Medicine
Volume 8
Issue 12
Background: Pathogenic variants in TGFBR1, TGFBR2 and SMAD3 genes cause Loeys-Dietz syndrome, and pathogenic variants in FBN1 cause Marfan syndrome. Despite their similar phenotypes, both syndromes may have different cardiovascular outcomes. Methods:
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::de03b5d1aae16af5302f62c019157997
https://hdl.handle.net/1854/LU-8639007
https://hdl.handle.net/1854/LU-8639007
Autor:
Vladimir Knezl, Zuzana Broskova, Ružena Sotníková, Viktor Bauer, Katarína Drábiková, Katalin Szöcs, Štefan Bezek, Jana Navarová, Zuzana Kyseľová, V Kristová, Peter Křenek, Ján Dřímal, Jana Nedelcevova, Iveta Bernatova, Ľudmila Okruhlicová, Viera Nosáľová
Publikováno v:
Interdisciplinary Toxicology
Protection of the vascular endothelium in experimental situationsOne of the factors proposed as mediators of vascular dysfunction observed in diabetes is the increased generation of reactive oxygen species (ROS). This provides support for the use of
Autor:
Christine Schröder, Lukáš Kubala, Denise Lau, Markus Sperandio, Claudia Nussbaum, Tanja K. Rudolph, Stephan Baldus, Daniel Benten, Anna Klinke, Katalin Szöcs, Paul G. Furtmüller, Kai Friedrichs, Hans-Jürgen Duchstein, Peter Heeringa, Heimo Ehmke, Karsten Sydow, Udo Schumacher, Volker Rudolph, Thomas Meinertz, Hans-Joachim Paust
Publikováno v:
Blood, 117(4), 1350-1358. AMER SOC HEMATOLOGY
Recruitment of polymorphonuclear neutrophils (PMNs) remains a paramount prerequisite in innate immune defense and a critical cofounder in inflammatory vascular disease. Neutrophil recruitment comprises a cascade of concerted events allowing for captu