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Archives of Gynecology and Obstetrics|February 7, 2019
Demographic changes and effects on the mode of delivery: a retrospective analysis of a large birth registry containing 27,729 singleton deliveries in a level I centerMarkus Huebner, Harald Abele, Christl Reisenauer, et al.Journal of Clinical Medicine|August 7, 2020
Living-Donor Uterus Transplantation: Pre-, Intra-, and Postoperative Parameters Relevant to Surgical Success, Pregnancy, and Obstetrics with Live BirthsSara Yvonne Brucker, Thomas Strowitzki, Florin-Andrei Taran, et al.Obesity (Silver Spring, Md.)|December 21, 2019
Maternal Weight, Weight Gain, and Metabolism are Associated with Changes in Fetal Heart Rate and VariabilityHaliza Mat Husin, Franziska Schleger, Ilena Bauer, et al.Archives of Gynecology and Obstetrics|January 9, 2026
Safety of a cytomegalovirus-specific hyperimmunoglobulin in the prevention of maternal-fetal transmission after primary infection-results of an open-label, single-arm, prospective trialKarl Oliver Kagan, Martin Enders, Michael Oliver Schneider, et al.Pathobiology : Journal of Immunopathology, Molecular and Cellular Biology|July 21, 2004
High apoptotic index correlates to p21 and p27 expression indicating a favorable outcome of primary breast cancer patients, but lacking prognostic significance in multivariate analysisThomas Schöndorf, Uwe-Jochen Göhring, Martina Becker, et al.Journal of Medical Genetics|November 6, 2021
Bi-allelic loss-of-function variants in KIF21A cause severe fetal akinesia with arthrogryposis multiplexRuth J Falb, Amelie J Müller, Wolfram Klein, et al.Recent Results in Cancer Research. Fortschritte Der Krebsforschung. Progres Dans Les Recherches Sur Le Cancer|January 17, 2003
Cisplatin, doxorubicin and paclitaxel induce mdr1 gene transcription in ovarian cancer cell linesThomas Schöndorf, Rainer Neumann, Carolin Benz, et al.Orphanet Journal of Rare Diseases|July 18, 2019
Clinical long-time course, novel mutations and genotype-phenotype correlation in a cohort of 27 families with POMT1-related disordersTobias Geis, Tanja Rödl, Haluk Topaloğlu, et al.American Journal of Human Genetics|February 17, 2015
Mutations in SEC24D, encoding a component of the COPII machinery, cause a syndromic form of osteogenesis imperfectaLutz Garbes, Kyungho Kim, Angelika Rieß, et al.Archives of Gynecology and Obstetrics|November 7, 2022
Uterine allograft removal by total laparoscopic hysterectomy after successful cesarean delivery in a living-donor uterus recipient with uterovaginal agenesis (MRKHS)Sara Yvonne Brucker, Bernhard Krämer, Harald Abele, et al.Pageof 15