Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Marlena Rohm"'
Autor:
Marlena Rohm, Gabriele Russo, Xavier Helluy, Martijn Froeling, Vincent Umathum, Nicolina Südkamp, Denise Manahan-Vaughan, Robert Rehmann, Johannes Forsting, Frank Jacobsen, Andreas Roos, Yoon Shin, Anne Schänzer, Matthias Vorgerd, Lara Schlaffke
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-12 (2023)
Abstract Quantitative muscle MRI is increasingly important in the non-invasive evaluation of neuromuscular disorders and their progression. Underlying histopathotological alterations, leading to changes in qMRI parameters are incompletely unraveled.
Externí odkaz:
https://doaj.org/article/3bd7a96d0a32465b92df1d3a2ab6a9e5
Autor:
Johannes Forsting, Marlena Rohm, Martijn Froeling, Anne-Katrin Güttsches, Nicolina Südkamp, Andreas Roos, Matthias Vorgerd, Lara Schlaffke, Robert Rehmann
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-2 (2024)
Externí odkaz:
https://doaj.org/article/0c4a8db7e3504c8dbd40da105823fe39
Autor:
Johannes Forsting, Marlena Rohm, Martijn Froeling, Anne-Katrin Güttsches, Nicolina Südkamp, Andreas Roos, Matthias Vorgerd, Lara Schlaffke, Robert Rehmann
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-10 (2022)
Abstract To evaluate differences in qMRI parameters of muscle diffusion tensor imaging (mDTI), fat-fraction (FF) and water T2 time in leg muscles of calpainopathy patients (LGMD R1/D4) compared to healthy controls, to correlate those findings to clin
Externí odkaz:
https://doaj.org/article/815aa00d380b4a2f959745644e150855
Autor:
Marlena Rohm, Leon Volke, Lara Schlaffke, Robert Rehmann, Nicolina Südkamp, Andreas Roos, Anne Schänzer, Andreas Hentschel, Matthias Vorgerd
Publikováno v:
Cells, Vol 12, Iss 12, p 1602 (2023)
Pompe disease is a rare genetic metabolic disorder caused by mutations in acid-alpha glucoside (GAA) leading to pathological lysosomal glycogen accumulation associated with skeletal muscle weakness, respiratory difficulties and cardiomyopathy, depend
Externí odkaz:
https://doaj.org/article/7a6e8d90f5014814bf8c059a78c72fa0
Autor:
Marlena Rohm, Caroline May, Katrin Marcus, Simone Steinbach, Verena Theis, Carsten Theiss, Veronika Matschke
Publikováno v:
Cellular Physiology and Biochemistry, Vol 52, Iss 6, Pp 1412-1426 (2019)
Externí odkaz:
https://doaj.org/article/4d5f73cdefdd413995c433ee49ba56aa
Autor:
Marlena Rohm, Marius Markmann, Johannes Forsting, Robert Rehmann, Martijn Froeling, Lara Schlaffke
Publikováno v:
Diagnostics, Vol 11, Iss 10, p 1747 (2021)
Quantitative MRI combines non-invasive imaging techniques to reveal alterations in muscle pathophysiology. Creating muscle-specific labels manually is time consuming and requires an experienced examiner. Semi-automatic and fully automatic methods red
Externí odkaz:
https://doaj.org/article/8d9a33858eac4fb8af984826d3995dbb
Autor:
Johannes Forsting, Marlena Rohm, Martijn Froeling, Anne-Katrin Güttsches, Matthias Vorgerd, Lara Schlaffke, Robert Rehmann
Publikováno v:
Diagnostics, Vol 11, Iss 9, p 1521 (2021)
Background: Muscle diffusion tensor imaging (mDTI) is a promising surrogate biomarker in the evaluation of muscular injuries and neuromuscular diseases. Since mDTI metrics are known to vary between different muscles, separation of different muscles i
Externí odkaz:
https://doaj.org/article/de87a20f8d334a01bafc4a3bdd8613eb
Autor:
Nadine Griesche, Judith Schilling, Stephanie Weber, Marlena Rohm, Verena Pesch, Frank Matthes, Georg Auburger, Sybille Krauss
Publikováno v:
Frontiers in Cellular Neuroscience, Vol 10 (2016)
Expansion of CAG repeats, which code for the disease-causing polyglutamine protein, is a common feature in polyglutamine diseases. RNA-mediated mechanisms that contribute to neuropathology in polyglutamine diseases are important. RNA-toxicity describ
Externí odkaz:
https://doaj.org/article/a544fa0a88524f8ba53acfd682d78b9c
Autor:
Elena Enax‐Krumova, Johannes Forsting, Marlena Rohm, Peter Schwenkreis, Martin Tegenthoff, Christine H. Meyer‐Frießem, Lara Schlaffke
Publikováno v:
European Journal of Neurology. 30:970-981
Autor:
Vorgerd, Marlena Rohm, Leon Volke, Lara Schlaffke, Robert Rehmann, Nicolina Südkamp, Andreas Roos, Anne Schänzer, Andreas Hentschel, Matthias
Publikováno v:
Cells; Volume 12; Issue 12; Pages: 1602
Pompe disease is a rare genetic metabolic disorder caused by mutations in acid-alpha glucoside (GAA) leading to pathological lysosomal glycogen accumulation associated with skeletal muscle weakness, respiratory difficulties and cardiomyopathy, depend