Zobrazeno 1 - 10
of 147
pro vyhledávání: '"Jan, Degenhardt"'
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::43c5653d9f2e78bb8206809cc97b44e4
https://doi.org/10.1002/pd.6302
https://doi.org/10.1002/pd.6302
Publikováno v:
Journal of Pediatric Urology. 18:116-126
The purpose of this retrospective cohort study was to compare the outcome of human fetuses with isolated severe lower urinary tract obstructions (LUTO) that were first treated before the completion of 16 weeks of gestation to fetuses first treated la
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f4c6ae170a6a4bfed8d392dd93f5e11c
https://doi.org/10.1016/j.jpurol.2022.01.002
https://doi.org/10.1016/j.jpurol.2022.01.002
Autor:
Ivonne, Bedei, Karl-Philipp, Gloning, Joyeux, Luc, 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.
Omphalocele is known to be associated with genetic anomalies like trisomy 13, 18 and Beckwith-Wiedemann syndrome, but not with Turner syndrome (TS). Our aim was to assess the incidence of omphalocele in fetuses with TS, the phenotype of this associat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::7527b99afb25e7039216d934cfeddb00
https://pubmed.ncbi.nlm.nih.gov/36600414
https://pubmed.ncbi.nlm.nih.gov/36600414
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
Autor:
Jan Degenhardt, Malgorzata Kolodziej, Roland Axt-Fliedner, Harald Ehrhardt, Frank Oehmke, D. Diehl, A Khaleeva, Thomas Kohl, Anita Windhorst, Eberhard Uhl, D. Faas, F. Belke, Bernd A. Neubauer
Publikováno v:
Obstetrical & Gynecological Survey. 76:319-321
Objective This observational study reports on the postnatal mortality and 30-month outcome of children who underwent fully percutaneous fetoscopic repair of myelomeningocele (MMC) at a single center in Giessen, Germany. Methods Between October 2010 a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::52be309735f25aa193ba07fc380f8ca3
https://doi.org/10.1097/01.ogx.0000754384.39211.28
https://doi.org/10.1097/01.ogx.0000754384.39211.28
Autor:
Aline Wolter, Jan Degenhardt, Rüdiger Stessig, J. Ritgen, Roland Axt-Fliedner, Malena Götte, Hakan Akintürk, Viktoria Kuhn, Markus Khalil, Christian Enzensberger, C. Vorisek, Andrii Kurkevych
Publikováno v:
Ultraschall in der Medizin - European Journal of Ultrasound. 43:e90-e97
Criss-cross heart (CCH) is a rare congenital cardiac defect defined by crossing of ventricular inflow streams contributing to less than 0.1 % of all congenital heart anomalies. Due to its rarity and complexity, prenatal diagnosis in these patients re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3d56f4368a1006be32110ea0c216a004
https://doi.org/10.1055/a-1205-0289
https://doi.org/10.1055/a-1205-0289
Autor:
Steven Willomeit, Andrii Kurkevych, Aline Wolter, Christian Enzensberger, Rüdiger Stessig, Jan Degenhardt, M. Goette, Carina Vorisek, S Bosselmann, G. Mielke, Maria Respondek-Liberska, Maciej Słodki, Roland Axt-Fliedner, Andrea Kawecki, J. Ritgen, Martin Krapp
Publikováno v:
Ultraschall in der Medizin - European Journal of Ultrasound. 42:291-296
Congenital corrected transposition of the great arteries (ccTGA) is a rare congenital cardiac anomaly which remains difficult to diagnose prenatally. We aim to investigate the natural history, associated anomalies and the outcome of patients in prena
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b4439cf8d10d5cc20976e68d48b72209
https://doi.org/10.1055/a-1069-7698
https://doi.org/10.1055/a-1069-7698
Autor:
Aline Wolter, Oliver Graupner, Jan Degenhardt, Andreea Kawecki, Thomas Kohl, Justus G. Reitz, Christian Enzensberger, Roland Axt-Fliedner
Publikováno v:
Prenatal Cardiology, Vol 2019, Iss 1, Pp 1-5 (2019)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::838c31a4400fcf98001b5de63d4e654a
https://doi.org/10.5114/pcard.2019.91331
https://doi.org/10.5114/pcard.2019.91331
Autor:
Ivonne Alexandra Bedei, Alexander Graf, Karl-Philipp Gloning, Matthias Meyer-Wittkopf, Daria Willner, Martin Krapp, Sabine Hentze, Alexander Scharf, Jan Degenhardt, Kai-Sven Heling, Peter Kozlowski, Kathrin Trautmann, Kai Jahns, Anne Geipel, Ismail Tekesin, Michael Elsässer, Lucas Wilhelm, Ingo Gottschalk, Jan-Erik Baumüller, Cahit Birdir, Felix Zöllner, Aline Wolter, Johanna Schenk, Tascha Gehrke, Corinna Keil, Jimmy Espinosa, Roland Axt-Fliedner
Publikováno v:
Journal of Clinical Medicine; Volume 11; Issue 15; Pages: 4588
Mirror syndrome is a rare and serious maternal condition associated with immune and non-immune fetal hydrops after 16 weeks of gestational age. Subjacent conditions associated with fetal hydrops may carry different risks for Mirror syndrome. Fetuses
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cd56e9b9c111d4d4eca46c9e6f5b3816
https://doi.org/10.3390/jcm11154588
https://doi.org/10.3390/jcm11154588
Autor:
Ivonne Bedei, Christian Enzensberger, Jan Degenhardt, Aline Wolter, Natalia Markert, Rüdiger Stressig, Oliver Graupner, J. Schenk, Roland Axt-Fliedner, Josef Thul, Markus Khalil, Andrii Kurkevych, J. Ritgen, Jan Sebastian Wolter, Christian Jux, C. Vorisek
Publikováno v:
Archives of Gynecology and Obstetrics
Objectives To analyse prenatal parameters predicting biventricular (BV) outcome in pulmonary atresia with intact ventricular septum/critical pulmonary stenosis (PAIVS/CPS). Methods We evaluated 82 foetuses from 01/08 to 10/18 in 3 centres in interval
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9d93fd8b48692215f47fce47131dfb6d
https://mediatum.ub.tum.de/doc/1618448/document.pdf
https://mediatum.ub.tum.de/doc/1618448/document.pdf
