Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Elisabeth Seidl"'
Autor:
Elisabeth Seidl-Mlczoch, Gregor Kasprian, Erwin Kitzmueller, Daniel Zimpfer, Irene Steiner, Victoria Jowett, Marlene Stuempflen, Alice Wielandner, Barbara Ulm, Ina Michel-Behnke
Publikováno v:
Frontiers in Pediatrics, Vol 10 (2022)
ObjectiveCardiac and extra-cardiac anomalies in 46 pre-natally diagnosed cases of heterotaxy were compared to post-natal anatomical patterns in order to reveal discordant findings. Second, the outcome of these fetuses was evaluated.MethodsFetuses wit
Externí odkaz:
https://doaj.org/article/02fb46b06ee94035aceff6a14001fe5b
Autor:
Stephanie Springer, Eva Karner, Elisabeth Seidl-Mlczoch, Guelen Yerlikaya-Schatten, Petra Pateisky, Barbara Ulm
Publikováno v:
Diagnostics, Vol 13, Iss 3, p 489 (2023)
Fetal dysrhythmias are common abnormalities, which can be categorized into three types: rhythm irregularities, tachyarrhythmias, and bradyarrhythmias. Fetal arrhythmias, especially in high-risk pregnancies, require special monitoring and treatment. T
Externí odkaz:
https://doaj.org/article/ecb75e4347584bc79f6d207b52e0363e
Autor:
Stephanie Springer, Eva Karner, Christof Worda, Maria Magdalena Grabner, Elisabeth Seidl-Mlczoch, Franco Laccone, Jürgen Neesen, Anke Scharrer, Barbara Ulm
Publikováno v:
Life, Vol 12, Iss 8, p 1223 (2022)
Fetal congenital heart disease (CHD) is often associated with chromosomal abnormalities. Our primary aim was to assess stillbirth and neonatal mortality rates for pregnancies complicated by trisomies 13, 18, and 21 in the presence of CHD, from a sing
Externí odkaz:
https://doaj.org/article/bad7dc1d84a54981975839f1452545e8
Autor:
Tim Zalewski, Daniela Prayer, Elisabeth Seidl-Mlczoch, Michael Weber, Vanessa Berger-Kulemann, Patricia A. Ulm, Barbara Ulm, G.O. Dovjak, Gregor Kasprian
Publikováno v:
Journal of the American College of Cardiology. 78:2312-2322
Knowledge about extracardiac anomalies (ECA) in fetal congenital heart disease (CHD) can improve our understanding of the developmental origins of various outcomes in these infants. The prevalence and spectrum of ECA, including structural brain anoma
Autor:
M. Stuempflen, Erwin Kitzmüller, Ina Michel-Behnke, Gregor Kasprian, Elisabeth Seidl-Mlczoch, Ahmed Ba-Ssalamah, Dana A. Muin, Daniel Zimpfer, Barbara Ulm, Daniela Prayer
Publikováno v:
Ultrasound in Obstetrics & Gynecology. 58:837-845
OBJECTIVE Heterotaxy or isomerism of the atrial appendages is a congenital disorder with variable presentation, associated with both cardiac and non-cardiac anomalies, which may have a serious impact on fetal outcome. The aim of this exploratory stud
Autor:
Gregor O. Dovjak, Georg Hausmaninger, Tim Zalewski, Victor Schmidbauer, Michael Weber, Christof Worda, Elisabeth Seidl-Mlczoch, Vanessa Berger-Kulemann, Daniela Prayer, Gregor J. Kasprian, Barbara Ulm
Publikováno v:
American journal of obstetrics and gynecology. 227(2)
Congenital heart disease is associated with an increased risk of smaller brain volumes and structural brain damage, and impaired growth of supratentorial brain structures in utero has been linked to poor neurodevelopmental outcomes. However, little i
Autor:
V. Berger-Kulemann, G. Schatten, G. Kasprian, Barbara Ulm, Ina Michel-Behnke, Elisabeth Seidl-Mlczoch
Publikováno v:
The Thoracic and Cardiovascular Surgeon.
Negative view slow-flow color Doppler: A potential improvement for first trimester cardiac screening
Autor:
Martin Metzenbauer, Elisabeth Seidl-Mlczoch, Hubertus Gregor, Erich Hafner, Ina Michel-Behnke
Publikováno v:
European Journal of Obstetrics & Gynecology and Reproductive Biology. 260:234-235
Autor:
Elisabeth Seidl
Publikováno v:
Das Handbuch Public Health ISBN: 9783709173145
In weiten Teilen der Welt, besonders im angelsachsischen Raum, ist Pflegewissenschaft schon seit Jahrzehnten als Fachdisziplin etabliert (vgl. z.B. Affara, 1995, S. 153, oder Axmacher, 1991, S. 120). Von den deutschsprachigen Landern, die in dieser H
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::eb286873c3772e8f08e73c3391039200
https://doi.org/10.1007/978-3-7091-6398-6_23
https://doi.org/10.1007/978-3-7091-6398-6_23