Zobrazeno 1 - 10
of 205
pro vyhledávání: '"Markus, Hoopmann"'
Autor:
Corinna Simonini, Markus Hoopmann, Karl Oliver Kagan, Torsten Schröder, Ulrich Gembruch, Annegret Geipel
Publikováno v:
BMC Pregnancy and Childbirth, Vol 22, Iss 1, Pp 1-8 (2022)
Abstract Background Wolf-Hirschhorn syndrome (WHS) is a common genetic condition and prenatal diagnosis is difficult due to heterogeneous expression of this syndrome and rather non-specific ultrasound findings. Objective of this study was to examine
Externí odkaz:
https://doaj.org/article/fc937a194c114a9e8593b3e04291c647
Publikováno v:
Diagnostics, Vol 13, Iss 3, p 539 (2023)
Placenta percreta occurs in about 5% of placenta accreta spectrum (PAS) and causes high maternal and fetal peripartum morbidity/mortality. A 34-year-old multiparous 4G2P (1xcesarean section (CS)) was admitted to hospital at the 34th week of gestation
Externí odkaz:
https://doaj.org/article/d1cb99a33d1b4f3e926a545c3741a214
Autor:
Tobias Geis, Tanja Rödl, Haluk Topaloğlu, Burcu Balci-Hayta, Sophie Hinreiner, Wolfgang Müller-Felber, Benedikt Schoser, Yasmin Mehraein, Angela Hübner, Birgit Zirn, Markus Hoopmann, Heiko Reutter, David Mowat, Gerhard Schuierer, Ulrike Schara, Ute Hehr, Heike Kölbel
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-17 (2019)
Abstract Background The protein O-mannosyltransferase 1, encoded by the POMT1 gene, is a key enzyme in the glycosylation of α-dystroglycan. POMT1–related disorders belong to the group of dystroglycanopathies characterized by a proximally pronounce
Externí odkaz:
https://doaj.org/article/6d36a41fe83e42eb90c37bc08b33293b
Publikováno v:
Archives of Gynecology and Obstetrics. 307:1839-1845
Three-dimensional (3D) ultrasound is an invaluable tool in the detection and evaluation of many uterine anomalies and improves upon the traditional approach of two-dimensional (2D) ultrasonography. We aim to describe an easy way of assessing the uter
Autor:
Sara Yvonne Brucker, Bernhard Krämer, Harald Abele, Melanie Henes, Markus Hoopmann, Dorit Schöller, Alfred Königsrainer, Hans Bösmüller, Konstantin Nikolaou, Patrick Krumm, Peter Rosenberger, Eckhard Heim, Bastian Amend, Steffen Rausch, Karina Althaus, Tamam Bakchoul, Martina Guthoff, Nils Heyne, Silvio Nadalin, Kristin Katharina Rall
Publikováno v:
Archives of Gynecology and Obstetrics. 307:827-840
Purpose To limit the burden of long-term immunosuppression (IS) after uterus transplantation (UTx), removal of the uterine allograft is indicated after maximum two pregnancies. Hitherto this has required graft hysterectomy by laparotomy. Our objectiv
Publikováno v:
Ultraschall in der Medizin - European Journal of Ultrasound. 43:550-569
Ovarian lesions have a wide range of sonomorphological features with numerous different underlying benign and malignant histologies. Based on the studies conducted by the International Ovarian Tumor Analysis (IOTA) group, ovarian masses can currently
Autor:
Andreas Dufke, Markus Hoopmann, Stephan Waldmüller, Natalia Carmen Prodan, Stefanie Beck‐Wödl, Ute Grasshoff, Tilman Heinrich, Angelika Riess, Martin Kehrer, Ruth J. Falb, Alexandra Liebmann, Cristiana Roggia, Miriam Stampfer, Malou Schadeck, Amelie J. Müller, Mona Grimmel, Petra Stöbe, Darja Gauck, Rebecca Buchert‐Lo, Sarah Baumann, Karin Schäferhoff, Miriam Bertrand, Benita Menden, Marc Sturm, Leon Schütz, Olaf Riess, Stephan Ossowski, Tobias B. Haack, Karl Oliver Kagan
Publikováno v:
Prenatal Diagnosis. 42:901-910
To examine the diagnostic yield of trio exome sequencing in fetuses with multiple structural defects with no pathogenic findings in cytogenetic and microarray analyses.We recruited 51 fetuses with two or more defects, non-immune fetal hydrops or feta
Publikováno v:
Archives of Gynecology and Obstetrics. 307:1285-1290
A systematic evaluation of the fetal anatomy as part of the second trimester ultrasound examination in pregnancy is useful in detecting pregnancy complications, fetal abnormalities, and genetic diseases. We aim to illustrate the basic and detailed se
Autor:
Natalia Carmen Prodan, Cornelia Wiechers, Annegret Geipel, Adeline Walter, Hans Jörg Siegmann, Peter Kozlowski, Markus Hoopmann, Karl Oliver Kagan
Publikováno v:
Fetal Diagnosis and Therapy. 49:85-94
Objective: The aim of the objective was to compare the detection rate for trisomy 21 of universal cell free DNA (cfDNA) screening with contingent screening. Methods: Retrospective study was carried out at 3 German centers. The study included euploid
Autor:
Peter, Oppelt, Helge, Binder, Jacques, Birraux, Sara, Brucker, Irene, Dingeldein, Ruth, Draths, Felicitas, Eckoldt, Ulrich, Füllers, Olaf, Hiort, Dorit, Hoffmann, Markus, Hoopmann, Jürgen, Hucke, Matthias, Korell, Maritta, Kühnert, Barbara, Ludwikowski, Hans-Joachim, Mentzel, Dan, Mon OʼDey, Katharina, Rall, Michael, Riccabona, Stefan, Rimbach, Norbert, Schäffeler, Sandra, Shavit, Raimund, Stein, Boris, Utsch, Rene, Wenzl, Peter, Wieacker, Mazen, Zeino
Publikováno v:
Geburtshilfe Frauenheilkd
Objectives Female genital malformations may be present in the form of individual entities, they may involve neighboring organs or they may occur in the context of complex syndromes. Given the anatomical structures of the vulva, vagina, uterus and ute