1.0Institut de Myologiehttps://www.institut-myologie.org/en/adminhttps://www.institut-myologie.org/en/author/admin/Monitoring disease progression in LGMD2I - Institut de Myologierich600338<blockquote class="wp-embedded-content" data-secret="3OKvrmnCqr"><a href="https://www.institut-myologie.org/en/2013/09/27/monitoring-disease-progression-in-lgmd2i/">Monitoring disease progression in LGMD2I</a></blockquote><iframe sandbox="allow-scripts" security="restricted" src="https://www.institut-myologie.org/en/2013/09/27/monitoring-disease-progression-in-lgmd2i/embed/#?secret=3OKvrmnCqr" width="600" height="338" title="“Monitoring disease progression in LGMD2I” — Institut de Myologie" data-secret="3OKvrmnCqr" frameborder="0" marginwidth="0" marginheight="0" scrolling="no" class="wp-embedded-content"></iframe><script type="text/javascript">
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Outcome measures for clinical trials in neuromuscular diseases are typically based on physical assessments, which are dependent on patient effort, combine the effort of different muscle groups, and may not be sensitive to progression over short trial periods in slow-progressing diseases. In this study, the authors hypothesised that quantitative fat imaging by MRI (Dixon technique) … [Read more]https://www.institut-myologie.org/wp-content/uploads/archive/en/plosonelogo_x155.jpg