Zobrazeno 1 - 10
of 71
pro vyhledávání: '"Stephan, Wenninger"'
Autor:
David Mal, Nina Döllinger, Erik Wolf, Stephan Wenninger, Mario Botsch, Carolin Wienrich, Marc Erich Latoschik
Publikováno v:
Frontiers in Virtual Reality, Vol 5 (2024)
Virtual humans play a pivotal role in social virtual environments, shaping users’ VR experiences. The diversity in available options and users’ individual preferences can result in a heterogeneous mix of appearances among a group of virtual human
Externí odkaz:
https://doaj.org/article/8ac81b9d9ecc42fba8a9e7575e4c1987
Autor:
Erik Wolf, Nina Döllinger, David Mal, Stephan Wenninger, Andrea Bartl, Mario Botsch, Marc Erich Latoschik, Carolin Wienrich
Publikováno v:
Frontiers in Virtual Reality, Vol 3 (2022)
Virtual reality applications employing avatar embodiment typically use virtual mirrors to allow users to perceive their digital selves not only from a first-person but also from a holistic third-person perspective. However, due to distance-related bi
Externí odkaz:
https://doaj.org/article/b83cf3b094744a209c025bb223a72925
Autor:
Nina Döllinger, Erik Wolf, David Mal, Stephan Wenninger, Mario Botsch, Marc Erich Latoschik, Carolin Wienrich
Publikováno v:
Frontiers in Virtual Reality, Vol 3 (2022)
Obesity is a serious disease that can affect both physical and psychological well-being. Due to weight stigmatization, many affected individuals suffer from body image disturbances whereby they perceive their body in a distorted way, evaluate it nega
Externí odkaz:
https://doaj.org/article/1154d5aca35b4b2a8ff2c50f901fac8e
Publikováno v:
Frontiers in Virtual Reality, Vol 2 (2021)
Realistic and lifelike 3D-reconstruction of virtual humans has various exciting and important use cases. Our and others’ appearances have notable effects on ourselves and our interaction partners in virtual environments, e.g., on acceptance, prefer
Externí odkaz:
https://doaj.org/article/d92d50d614fd4495b4839335231cba47
Publikováno v:
Frontiers in Virtual Reality, Vol 2 (2021)
3D morphable models are widely used to describe the variation of human body shapes. However, these models typically focus on the surface of the human body, since the acquisition of the volumetric interior would require prohibitive medical imaging. In
Externí odkaz:
https://doaj.org/article/fbfaece5686e4c778e2c84ad40f2d062
Autor:
Lukacs Zoltan, Paulina Nieves Cobos, Stephan Wenninger, Tracey A. Willis, Michela Guglieri, Marc Roberts, Rosaline Quinlivan, David Hilton-Jones, Teresinha Evangelista, Stephan Zierz, Beate Schlotter-Weigel, Maggie C Walter, Peter Reilich, Thomas Klopstock, Marcus Deschauer, Volker Straub, Wolfgang Müller-Felber, Benedikt Schoser
Publikováno v:
Нервно-мышечные болезни, Vol 6, Iss 3, Pp 24-27 (2019)
Externí odkaz:
https://doaj.org/article/4ec0d1645281460598905760d4b17f8a
Publikováno v:
Journal of Neurology. 270:250-261
Background Spinal muscular atrophy (SMA) is an autosomal recessive neuromuscular disorder caused by mutations in the SMN gene, leading to progressive muscular weakness, atrophy and so far neglected musculoskeletal pain. This study is the first to cha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5affc7900715666da89a37b8cf24ef2a
https://doi.org/10.1007/s00415-022-11351-0
https://doi.org/10.1007/s00415-022-11351-0
Autor:
Kristina Gutschmidt, Corinna Wirner-Piotrowski, Natalia García Angarita, Federica Montagnese, Benedikt Schoser, Stephan Wenninger
Publikováno v:
Neuromuscular Disorders.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::81f87461d6ad5c41eade8f555e4bbf69
https://doi.org/10.1016/j.nmd.2023.05.002
https://doi.org/10.1016/j.nmd.2023.05.002
Autor:
Stephan Wenninger
Publikováno v:
Notfallmedizin up2date. 17:189-206
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8eac8dc4fad0bc394785af52b8ca7ad6
https://doi.org/10.1055/a-1500-4451
https://doi.org/10.1055/a-1500-4451
Publikováno v:
Frontiers in Neurology, Vol 9 (2018)
Myotonic dystrophy type 1 (DM1) and type 2 (DM2) represent the most frequent multisystemic muscular dystrophies in adulthood. They are progressive, autosomal dominant diseases caused by an abnormal expansion of an unstable nucleotide repeat located i
Externí odkaz:
https://doaj.org/article/16dfa42aa47c471bbab3374850611a69