Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Kathrin Trautmann"'
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
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:
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:
Hendryk Pilch, Kathrin Trautmann, Claudia Fusshoeller, Marcus Schmidt, Cordula Franz, Debra K. Kelleher, Hawighorst-Knapstein S, Paul Georg Knapstein, Peter Vaupel, Goetz Schoenefuss, Heinz Koelbl
Publikováno v:
Gynecologic Oncology. 94:398-403
Objective . To evaluate the impact of treatment for genital cancer on quality of life and body image to determine patients' therapy-related needs for quality improvement of medical care before and after surgery. Methods . We started to evaluate women
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1c6164a0a7f03fd2c2ff63550b599425
https://doi.org/10.1016/j.ygyno.2004.04.025
https://doi.org/10.1016/j.ygyno.2004.04.025