Zobrazeno 1 - 10
of 133
pro vyhledávání: '"Ursula, Plöckinger"'
Autor:
Ursula Plöckinger, Ulrike Ernst-Auga
Publikováno v:
Religions, Vol 15, Iss 8, p 909 (2024)
We discuss the concept of a ‘body’, the individual body as the lived experience of the body, the social body, shaped by the tensions between the demands of a social/moral order and the egocentric drives, and the body politic, as an institutionali
Externí odkaz:
https://doaj.org/article/946bb6c963594a44a7a263b0405a619c
Autor:
Ursula Plöckinger, Ulrike Auga
Publikováno v:
Religions, Vol 13, Iss 11, p 1118 (2022)
The four principles of Western medical bioethics, i.e., autonomy, nonmaleficence, beneficence and justice, published by Beauchamps and Childress in their seminal ‘Principles of Biomedical Ethics’, are understood as universal. However, Non-Western
Externí odkaz:
https://doaj.org/article/8910d05e1d314a36affe52c123b4e40e
Autor:
Radu Tanacli, Jan‐Hendrik Hassel, Rolf Gebker, Alexander Berger, Michael Gräfe, Christopher Schneeweis, Patrick Doeblin, Eckart Fleck, Christian Stehning, Frank Tacke, Burkert Pieske, Joachim Spranger, Ursula Plöckinger, Athanasia Ziagaki, Sebastian Kelle
Publikováno v:
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, Vol 10, Iss 17 (2021)
Background Phenylketonuria is the most common inborn error of amino acid metabolism, where oxidative stress and collateral metabolic abnormalities are likely to cause cardiac structural and functional modifications. We aim herein to characterize the
Externí odkaz:
https://doaj.org/article/deada281ee8947dd980d62941347cdfe
Autor:
Aline Azabdaftari, Markus van der Giet, Mirjam Schuchardt, Julia B. Hennermann, Ursula Plöckinger, Uwe Querfeld
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-11 (2019)
Abstract Background Patients with Phenylketonuria (PKU) are exposed to multiple cardiovascular risk factors, but the clinical significance of these abnormalities is yet unknown. The purpose of this study was to characterize the cardiovascular phenoty
Externí odkaz:
https://doaj.org/article/fd66fdb8fa424549b648d26b220ca3e3
Autor:
Fiona J. Stewart, Andrew Bentley, Barbara K. Burton, Nathalie Guffon, Susan L. Hale, Paul R. Harmatz, Susanne G. Kircher, Pavan K. Kochhar, John J. Mitchell, Ursula Plöckinger, Sue Graham, Stephen Sande, Zlatko Sisic, Tracey A. Johnston
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 8, Iss C, Pp 111-115 (2016)
The mucopolysaccharidoses (MPS disorders) are rare inherited diseases associated with multi-organ accumulation of glycosaminoglycans, leading to musculoskeletal, respiratory, cardiac, neurological, ophthalmological, otolaryngological, and gastrointes
Externí odkaz:
https://doaj.org/article/86406aef95dc4f2fac4a8c60041dc322
Autor:
Anca Zimmermann, Rüdiger Zwerenz, Michael Droste, Christof Schöfl, Christian J. Strasburger, Ursula Plöckinger, Athanasia Ziagaki, Jürgen Honegger, Anne Dixius, Bledar Millaku, Gerrit Toenges, Manfred E. Beutel, Matthias M. Weber
Publikováno v:
Frontiers in Endocrinology, Vol 9 (2018)
Objective: Acromegalic patients display a distinct neuropsychological profile and suffer from chronic physical complaints. We aimed to investigate in more detail these aspects in acromegalic patients, dependent on influencing factors like disease act
Externí odkaz:
https://doaj.org/article/e4ea5d3d42284b01a7e606dacc775a83
Autor:
Auga, Ursula Plöckinger, Ulrike
Publikováno v:
Religions; Volume 13; Issue 11; Pages: 1118
The four principles of Western medical bioethics, i.e., autonomy, nonmaleficence, beneficence and justice, published by Beauchamps and Childress in their seminal ‘Principles of Biomedical Ethics’, are understood as universal. However, Non-Western
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=multidiscipl::b5278bf903767a569bb7ae257f121611
Autor:
Karina Grohmann‐Held, Peter Burgard, Christoph G. O. Baerwald, Skadi Beblo, Stephan vom Dahl, Anibh Das, Katharina Dokoupil, Sandra Fleissner, Peter Freisinger, Margret Heddrich‐Ellerbrok, Alexandra Jung, Vanessa Korpel, Johannes Krämer, Dinah Lier, Esther M. Maier, Uta Meyer, Chris Mühlhausen, Martha Newger, Ulrike Och, Ursula Plöckinger, Stefanie Rosenbaum‐Fabian, Frank Rutsch, René Santer, Petra Schick, Martin Schwarz, Ute Spiekerkötter, Ursula Strittmatter, Alena G. Thiele, Athanasia Ziagaki, Ulrike Mütze, Florian Gleich, Sven F. Garbade, Stefan Kölker
Publikováno v:
Journal of inherited metabolic diseaseREFERENCES. 45(6)
To prevent maternal phenylketonuria (PKU) syndrome low phenylalanine concentrations (target range, 120-360 μmol/L) during pregnancy are recommended for women with PKU. We evaluated the feasibility and effectiveness of current recommendations and ide
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d73c92a48559927d2d1c35868aad7268
https://pubmed.ncbi.nlm.nih.gov/36054426
https://pubmed.ncbi.nlm.nih.gov/36054426
Autor:
Fiona Stewart MB, BS, Andrew Bentley MD, Barbara K Burton MD, Nathalie Guffon MD, Susan L. Hale MN, ARNP, Paul R. Harmatz MD, Susanne G. Kircher MD, Pavan K. Kochhar MD, John J. Mitchell MD, Ursula Plöckinger MD, Jennifer Semotok MSc, PhD, Sue Graham MSc, Stephen Sande PhD, Zlatko Sisic MD, Tracey A. Johnston MD
Publikováno v:
Journal of Inborn Errors of Metabolism and Screening, Vol 4 (2016)
The mucopolysaccharidosis (MPS) disorders are rare genetic diseases caused by deficiencies in lysosomal enzymes involved in the degradation of glycosaminoglycans, leading to pulmonary, cardiac and neurological dysfunctions, skeletal anomalies, impair
Externí odkaz:
https://doaj.org/article/88cc6463f86e47efa9e1e16fd5f5f9fd
Autor:
Martin Schwarz, Julia B. Hennermann, Stephan vom Dahl, Annemarie Klimek, Ursula Plöckinger, Frank Rutsch, Margret Heddrich-Ellerbrok, F Lang, Klaus Schöne, Markus Ott, Klaus G Parhofer, Christoph Baerwald
Publikováno v:
Annals of Nutrition and Metabolism. 76:251-258
Background: Only few data on dietary management of adult phenylketonuria (PKU) patients are published. Objectives: This study aimed to assess living situation, dietary practices, and health conditions of early-treated adult PKU patients. Methods: A t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::852231ae3a07cc63aac22023656ad221
https://doi.org/10.1159/000510260
https://doi.org/10.1159/000510260