Zobrazeno 1 - 10
of 582
pro vyhledávání: '"Sabine Krause"'
Autor:
Katja C. Senn, Simone Thiele, Laura Gumbert, Sabine Krause, Maggie C. Walter, Klaus H. Nagels
Publikováno v:
Health and Quality of Life Outcomes, Vol 21, Iss 1, Pp 1-11 (2023)
Abstract Background To understand the health-related quality of life (HRQoL) in inclusion body myositis (IBM) from a holistic perspective on the background of a complex care situation. The focus was on how the patient journey may be structured over t
Externí odkaz:
https://doaj.org/article/53e5a4b74c7f47b5b60241d845e44125
Autor:
Per-Ole Carstens, Luisa M. Müllar, Arne Wrede, Sabrina Zechel, Martin M. Wachowski, Almuth Brandis, Sabine Krause, Stephan Zierz, Jens Schmidt
Publikováno v:
Frontiers in Immunology, Vol 14 (2023)
IntroductionWe aimed to identify B-cell-mediated immunomechanisms in inclusion body myositis (IBM) and polymyositis (PM) as part of the complex pathophysiology.Materials and methodsHuman primary myotube cultures were derived from orthopedic surgery.
Externí odkaz:
https://doaj.org/article/23060bdf8e2743068f853639ee4aa7c1
Autor:
Katja C. Senn, Laura Gumbert, Simone Thiele, Sabine Krause, Maggie C. Walter, Klaus H. Nagels
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 17, Iss 1, Pp 1-15 (2022)
Abstract Background Inclusion body myositis (IBM) is a rare neuromuscular disease (NMD) and effective therapies are not available. Thus, it is relevant to determine the health-related quality of life (HRQoL) in IBM patients including aspects of menta
Externí odkaz:
https://doaj.org/article/d04be4ed591b44ceb60553b7cde4074e
Autor:
Fabian Hofmeister, Lisa Baber, Uta Ferrari, Stefan Hintze, Stefanie Jarmusch, Sabine Krause, Peter Meinke, Stefan Mehaffey, Carl Neuerburg, Fabiana Tangenelli, Benedikt Schoser, Michael Drey
Publikováno v:
BMC Neurology, Vol 21, Iss 1, Pp 1-9 (2021)
Abstract Background Sarcopenia is the age-related loss of muscle mass and strength. Undiagnosed late-onset neuromuscular disorders need to be considered in the differential diagnosis of sarcopenia. Aim Based on emblematic case reports and current neu
Externí odkaz:
https://doaj.org/article/6a4938f4acb643c28d120c9301611016
Autor:
Michael Stirm, Lina Marie Fonteyne, Bachuki Shashikadze, Magdalena Lindner, Maila Chirivi, Andreas Lange, Clara Kaufhold, Christian Mayer, Ivica Medugorac, Barbara Kessler, Mayuko Kurome, Valeri Zakhartchenko, Arne Hinrichs, Elisabeth Kemter, Sabine Krause, Rüdiger Wanke, Georg J. Arnold, Gerhard Wess, Hiroshi Nagashima, Martin Hrabĕ de Angelis, Florian Flenkenthaler, Levin Arne Kobelke, Claudia Bearzi, Roberto Rizzi, Andrea Bähr, Sven Reese, Kaspar Matiasek, Maggie C. Walter, Christian Kupatt, Sibylle Ziegler, Peter Bartenstein, Thomas Fröhlich, Nikolai Klymiuk, Andreas Blutke, Eckhard Wolf
Publikováno v:
Disease Models & Mechanisms, Vol 14, Iss 12 (2021)
Large-animal models for Duchenne muscular dystrophy (DMD) are crucial for the evaluation of diagnostic procedures and treatment strategies. Pigs cloned from male cells lacking DMD exon 52 (DMDΔ52) exhibit molecular, clinical and pathological hallmar
Externí odkaz:
https://doaj.org/article/d8939e99103646a0a9090e1ac2200524
Autor:
Tina Donandt, Stefan Hintze, Sabine Krause, Eckhard Wolf, Benedikt Schoser, Maggie C. Walter, Peter Meinke
Publikováno v:
Life, Vol 12, Iss 10, p 1668 (2022)
Duchenne muscular dystrophy (DMD) is the most frequent genetic myopathy in childhood and leads to progressive muscle atrophy, weakness, and premature death. So far, there is no curative treatment available. Therapeutic development from bench to bedsi
Externí odkaz:
https://doaj.org/article/b5ed86dd25f04376951a37029f5ad1ec
Autor:
Anne-Katrin Guettsches, Nancy Meyer, René P. Zahedi, Teresinha Evangelista, Thomas Muentefering, Tobias Ruck, Emmanuelle Lacene, Christoph Heute, Humberto Gonczarowska-Jorge, Benedikt Schoser, Sabine Krause, Andreas Hentschel, Matthias Vorgerd, Andreas Roos
Publikováno v:
Biomedicines, Vol 10, Iss 10, p 2443 (2022)
Dominant VCP–mutations cause a variety of neurological manifestations including inclusion body myopathy with early–onset Paget disease and frontotemporal dementia 1 (IBMPFD). VCP encodes a ubiquitously expressed multifunctional protein that is a
Externí odkaz:
https://doaj.org/article/01e33abb37a14f4589274c424ffffc0e
Autor:
Suzan M Hammond, Annemieke Aartsma‐Rus, Sandra Alves, Sven E Borgos, Ronald A M Buijsen, Rob W J Collin, Giuseppina Covello, Michela A Denti, Lourdes R Desviat, Lucía Echevarría, Camilla Foged, Gisela Gaina, Alejandro Garanto, Aurelie T Goyenvalle, Magdalena Guzowska, Irina Holodnuka, David R Jones, Sabine Krause, Taavi Lehto, Marisol Montolio, Willeke Van Roon‐Mom, Virginia Arechavala‐Gomeza
Publikováno v:
EMBO Molecular Medicine, Vol 13, Iss 4, Pp n/a-n/a (2021)
Abstract Nucleic acid‐based therapeutics that regulate gene expression have been developed towards clinical use at a steady pace for several decades, but in recent years the field has been accelerating. To date, there are 11 marketed products based
Externí odkaz:
https://doaj.org/article/76e52486fd764de6bb07b4e5106b079a
Autor:
Alexander Schmölz, Sabine Krause
Publikováno v:
MedienPädagogik: Zeitschrift für Theorie und Praxis der Medienbildung, Vol 29, Pp 17-34 (2017)
Dieser Beitrag verortet Medienpädagogik im Feld der Wissenschaften. Es wird die Frage diskutiert, inwieweit ein eigenständiger Zugang der Medienpädagogik zu ihren Forschungsanliegen als grundlegend für die Konstitution einer wissenschaftlichen Di
Externí odkaz:
https://doaj.org/article/51314e0e33914be1ac880a141f61a407
Publikováno v:
Medienimpulse, Vol 55, Iss 4 (2018)
Externí odkaz:
https://doaj.org/article/8e9bf452e58a43daa458dc42d8b41d08