Zobrazeno 1 - 10
of 163
pro vyhledávání: '"Hans H. Jung"'
Autor:
Ruth H. Walker, Mariana Barreto, James R. Bateman, M. Leonor Bustamante, Graham Chiu, Scott Feitell, Beat M. Frey, Patricio Guerra, Sofia Guerrero, Hans H. Jung, Fernando Maldonado, Eduardo Meyer, Marcelo Miranda, Emelie McFarland, Patricia Oates, Gorka Ochoa, Karin Olsson, Martin Paucar, Jonatan Alvarez Proschle, Esther M. Sammler, Monica Troncoso, Rachel Wu-Wallace, Leo Young, Sunitha Vege, Connie M. Westhoff, Adrian Danek
Publikováno v:
Frontiers in Neuroscience, Vol 18 (2024)
XK disease is a very rare, multi-system disease, which can present with a wide spectrum of symptoms. This disorder can also be identified pre-symptomatically with the incidental detection of serological abnormalities when typing erythrocytes in perip
Externí odkaz:
https://doaj.org/article/6593764dccbd407cabe77da3d2d6c3c6
Autor:
Sofie Brouwers, Raphael Heimgartner, Natallia Laptseva, Adriano Aguzzi, Niklas F. Ehl, Thomas Fehr, Felicitas Hitz, Hans H. Jung, Joel Kälin, Markus G. Manz, Beat Müllhaupt, Frank Ruschitzka, Harald Seeger, Georg Stussi, Markus Zweier, Andreas J. Flammer, Bernhard Gerber, Rahel Schwotzer
Publikováno v:
Swiss Medical Weekly, Vol 154, Iss 2 (2024)
AIMS OF THE STUDY: Systemic amyloidoses are rare protein-folding diseases with heterogeneous, often nonspecific clinical presentations. To better understand systemic amyloidoses and to apply state-of-the-art diagnostic pathways and treatment, the int
Externí odkaz:
https://doaj.org/article/cf69857cee974352a0bcd0080184335f
Publikováno v:
Contact, Vol 6 (2023)
The two very rare neurodegenerative diseases historically known as the “neuroacanthocytosis syndromes” are due to mutations of either VPS13A or XK. These are phenotypically similar disorders that affect primarily the basal ganglia and hence resul
Externí odkaz:
https://doaj.org/article/46945deddc38488394f8024b85d824e9
Autor:
Eileen Neumann Dr. med., Lisa Ballmer MSc, Olivia Studhalter BSc, Nicole Schmid Dr. phil., Hans H. Jung Prof.
Publikováno v:
Gerontology and Geriatric Medicine, Vol 9 (2023)
Background: The COVID-19 pandemic had a significant impact on the Swiss health care system, affecting especially vulnerable people, such as patients suffering from dementia. The purpose of this study was to investigate the challenges experienced by d
Externí odkaz:
https://doaj.org/article/04b6625a3cab4fd19afd61f22c7ec7b1
Autor:
Aurel B. Leuchtmann, Sandro Manuel Mueller, David Aguayo, Jens A. Petersen, Maria Ligon-Auer, Martin Flück, Hans H. Jung, Marco Toigo
Publikováno v:
Scientific Reports, Vol 10, Iss 1, Pp 1-10 (2020)
Abstract Skeletal muscle capillarization is a determining factor in gas and metabolite exchange, while its impairments may contribute to the development of sarcopenia. Studies on the potential of resistance training (RT) to induce angiogenesis in old
Externí odkaz:
https://doaj.org/article/bf03df4e78884107ba8ba6e4db00b16b
Autor:
Hans H. Jung, Franz M.J. Pfister
Publikováno v:
Technology Innovation Management Review, Vol 10, Iss 2, Pp 14-24 (2020)
Written informed consent (WIC) is required in the context of voluntary participation in a clinical trial. The trial participant gives WIC in accordance with various regulatory requirements. We present a framework concept for a blockchain-based distri
Externí odkaz:
https://doaj.org/article/9c2312354a454045bcc11fb13d2e1089
Autor:
Adalgisa Condoluci, Marie Théaudin, Rahel Schwotzer, Aju P. Pazhenkottil, Paolo Arosio, Manuela Averaimo, Ulrike Bacher, Peter Bode, Andrea Cavalli, Stefan Dirnhofer, Nadia Djerbi, Stephan Dobner, Thomas Fehr, Maura Garofalo, Ariana Gaspert, Sabine Gerull, Raphael Heimgartner, Annemarie Hübers, Hans H. Jung, Chiara Kessler, Raphael Knöpfel, Natallia Laptseva, Giulia Magini, Robert Manka, Luca Mazzucchelli, Martin Meyer, Violeta Mihaylova, Pierre Monney, Alessio Mylonas, René Nkoulou, Thomas Pabst, Otmar Pfister, Axel Rüfer, Adrian Schmidt, Harald Seeger, Simon F. Stämpfli, Guido Stirnimann, Thomas Suter, Giorgio Treglia, Alexandar Tzankov, Friederike Vetter, Markus Zweier, Andreas J. Flammer, Bernhard Gerber
Publikováno v:
Swiss Medical Weekly, Vol 151, Iss 4142 (2021)
This article was corrected and republished online on November 4, 2021. Please see Erratum (Swiss Med Wkly. 2021;151:w30104)
Externí odkaz:
https://doaj.org/article/a2cc0239496a4b7e934b23762969b699
Autor:
Sandro Manuel Mueller, Violeta Mihaylova, Sebastian Frese, Jens A. Petersen, Maria Ligon-Auer, David Aguayo, Martin Flück, Hans H. Jung, Marco Toigo
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-5 (2019)
Abstract Background Skeletal muscle wasting is a hallmark of Huntington’s disease (HD). However, data on myocellular characteristics and myofiber remodeling in HD patients are scarce. We aimed at gaining insights into myocellular characteristics of
Externí odkaz:
https://doaj.org/article/bd6649abb3a34995ac432bb70b57e9e9
Publikováno v:
Tremor and Other Hyperkinetic Movements, Pp 1-10 (2019)
Background: Huntington’s disease (HD) is a rare, progressive neurodegenerative disease. Currently, there is no cure for the disease, but treatment may alleviate HD symptoms. In recent years, several exercise training interventions have been conduct
Externí odkaz:
https://doaj.org/article/81c18bf0c520462b90ee6b691c9c9e73
Autor:
Rahel Schwotzer, Andreas J. Flammer, Sabine Gerull, Thomas Pabst, Paolo Arosio, Manuela Averaimo, Ulrike Bacher, Peter Bode, Andrea Cavalli, Adalgisa Condoluci, Stefan Dirnhofer, Nadia Djerbi, Stephan W. Dobner, Thomas Fehr, Maura Garofalo, Ariana Gaspert, Raphael Heimgartner, Annemarie Hübers, Hans H. Jung, Chiara Kessler, Raphael Knöpfel, Natallia Laptseva, Robert Manka, Luca Mazzucchelli, Martin Meyer, Violeta Mihaylova, Pierre Monney, Alessio Mylonas, René Nkoulou, Aju P. Pazhenkottil, Otmar Pfister, Axel Rüfer, Adrian Schmidt, Harald Seeger, Simon F. Stämpfli, Guido Stirnimann, Thomas Suter, Marie Théaudin, Giorgio Treglia, Alexandar Tzankov, Friederike Vetter, Markus Zweier, Bernhard Gerber
Publikováno v:
Swiss Medical Weekly, Vol 150, Iss 4950 (2020)
Systemic amyloidosis is a heterogeneous group of diseases associated with protein misfolding into insoluble beta-sheet rich structures that deposit extracellularly in different organs, eventually compromising their function. There are more than 30 di
Externí odkaz:
https://doaj.org/article/0e5c75901fcc4911aff0d76ae3910380