Zobrazeno 1 - 10
of 359
pro vyhledávání: '"Roland Axt-Fliedner"'
Autor:
Mateja Pfeifer, Helga Rehder, Maria Gerykova Bujalkova, Christine Bartsch, Barbara Fritz, Cordula Knopp, Björn Beckers, Frank Dohle, Matthias Meyer-Wittkopf, Roland Axt-Fliedner, Alexander V. Beribisky, Manuel Hofer, Franco Laccone, Katharina Schoner
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-11 (2024)
Abstract Background In this study we aimed to describe the morphological and pathogenetic differences between tracheal agenesis and tracheal atresia, which are not clearly distinguished from each other in the literature, and to contribute thereby to
Externí odkaz:
https://doaj.org/article/a27bc7de37c240fbb01c3dfa427cba1f
Autor:
Justus G. Reitz, MD, David Zurakowski, MS, PhD, Viktoria A. Kuhn, MD, Johnathan Murnick, MD, Mary T. Donofrio, MD, Yves d'Udekem, MD, Daniel Licht, MD, Agnieszka Kosiorek, MD, Catherine Limperopoulos, PhD, Roland Axt-Fliedner, MD, Can Yerebakan, MD, Jessica L. Carpenter, MD
Publikováno v:
JTCVS Open, Vol 17, Iss , Pp 229-247 (2024)
Objectives: Brain injury is commonly seen on magnetic resonance imaging in infants with complex congenital heart disease. The impact of perioperative brain injury on neurodevelopmental outcomes is not well understood. We evaluate the association of b
Externí odkaz:
https://doaj.org/article/c8862ef1093c4356b1d8a849da5c76e7
Autor:
Aruna Marchetto, Susanne Leidescher, Theresia van Hoi, Niklas Hirschberger, Florian Vogel, Siegmund Köhler, Ivonne Alexandra Bedei, Roland Axt-Fliedner, Moneef Shoukier, Corinna Keil
Publikováno v:
Life, Vol 14, Iss 5, p 628 (2024)
Fryns syndrome (FS) is a multiple congenital anomaly syndrome with different multisystemic malformations. These include congenital diaphragmatic hernia, pulmonary hypoplasia, and craniofacial dysmorphic features in combination with malformations of t
Externí odkaz:
https://doaj.org/article/2728a72c1ee44fb285eda6d595e31ab5
Autor:
Roland Axt-Fliedner, Asia Nazar, Ivonne Bedei, Johanna Schenk, Maleen Reitz, Stefan Rupp, Christian Jux, Aline Wolter
Publikováno v:
Diagnostics, Vol 14, Iss 3, p 238 (2024)
We aimed to evaluate retrospectively associated anomalies and outcome in prenatal aortic arch anomalies (AAAs). We included ninety patients with aberrant right subclavian artery (ARSA), right aortic arch (RAA) with mirror image branching (RAA-mirror)
Externí odkaz:
https://doaj.org/article/9b41969c9b55483c80ac586c89a230c7
Autor:
Maciej Słodki, Katarzyna-Zych-Krekora, Roland Axt-Fliedner, Ana Bianchi, Edward Araujo Junior, Isaac Blickstein, Sefa Kelekci, Lami Yeo, Jay D. Pruetz, Giuseppe Rizzo, Neil Seligman, Mark Sklansky, Luc de Catte, Stuart Weiner, Frank Chervenak, Jader Cruz, Andrii Kurkevych, Michał Krekora, Maria Respondek-Liberska
Publikováno v:
Journal of Ultrasonography, Vol 16, Iss 64, Pp 94-96 (2016)
Congenital heart defects are among the most common congenital defects and contribute substantially to the mortality of newborns and young infants, in spite of well-developed medical and surgical treatments.
Externí odkaz:
https://doaj.org/article/ae5bae1edb03430eb48299cf2aba2831
Autor:
Christian Enzensberger, Friederike Achterberg, Jan Degenhardt, Aline Wolter, Oliver Graupner, Johannes Herrmann, Roland Axt-Fliedner
Publikováno v:
Ultrasound International Open, Vol 03, Iss 01, Pp E26-E33 (2017)
Objective The primary objective of this study was to determine the feasibility and reproducibility of 2-dimensional speckle tracking imaging based on the wall motion tracking (WMT) technique in fetal echocardiography. The secondary objective was to c
Externí odkaz:
https://doaj.org/article/577d6051628740708b0be657fde9b823
Publikováno v:
Case Reports in Obstetrics and Gynecology, Vol 2014 (2014)
Body stalk anomaly is a rare and severe malformation syndrome in which the exact pathophysiology and trigger factors are still unknown. This is a case of a 30-year-old patient who underwent ultrasound at 9 weeks of gestation. It revealed an abnormal
Externí odkaz:
https://doaj.org/article/527d4d4751aa4ae98bb82d6ebebb9ad8
Autor:
Edward Araujo Júnior, Luiza Graça Coutinho, Nathalie Jeanne Bravo-Valenzuela, Patrícia Aquino, Luciane Alves da Rocha, Giuseppe Rizzo, Gabriele Tonni, Maria Respondek-Liberska, Maciej Slodki, Aline Wolter, Roland Axt-Fliedner
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::895b0ab85ebd2dc58c62ade50e3e7e71
https://hdl.handle.net/2108/320197
https://hdl.handle.net/2108/320197
Autor:
Ivonne Bedei, Karl‐Philipp Gloning, Luc Joyeux, Matthias Meyer‐Wittkopf, Daria Willner, Martin Krapp, Alexander Scharf, Jan Degenhardt, Kai‐Sven Heling, Peter Kozlowski, Kathrin Trautmann, Kai M. Jahns, Annegret Geipel, Ismail Tekesin, Michael Elsässer, Lucas Wilhelm, Ingo Gottschalk, Jan‐Erik Baumüller, Cahit Birdir, Andreas Schröer, Felix Zöllner, Aline Wolter, Johanna Schenk, Tascha Gehrke, Alicia Spaeth, Roland Axt‐Fliedner
Publikováno v:
Prenatal Diagnosis. 43:183-191
Autor:
Michaela Möginger, Nadine Mand, Katharina Schoner, Maria Seipelt, Maximilian Schulze, Siegmund Köhler, Roland Axt-Fliedner, Corinna Nora Keil
Publikováno v:
Zeitschrift für Geburtshilfe und Neonatologie. 226:416-421
ZusammenfassungSeit Beginn der Pandemie dominiert die SARS-CoV-2-Infektion den klinischen Alltag. In der Behandlung von Hochrisikopopulationen bestand lange Unklarheit über das Ausmaß und die Konsequenzen der Infektion. Zu diesem Risikokollektiv ge