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Journal of Neurology, Neurosurgery, and Psychiatry|December 24, 2014
Bethlem myopathy: long-term follow-up identifies COL6 mutations predicting severe clinical evolutionN Deconinck, P Richard, V Allamand, et al.Neuromuscular Disorders : NMD|November 16, 2019
MYO-MRI diagnostic protocols in genetic myopathiesJodi Warman Chardon, Jordi Díaz-Manera, Giorgio Tasca, et al.Acta Neuropathologica|February 1, 2019
ACTN2 mutations cause "Multiple structured Core Disease" (MsCD)Xavière Lornage, Norma B Romero, Claire A Grosgogeat, et al.Muscle & Nerve|August 2, 2018
Muscle imaging in laminopathies: Synthesis study identifies meaningful muscles for follow-upDavid GóMez-Andrés, Jordi Díaz-Manera, Aida Alejaldre, et al.Journal of Neurology|September 27, 2019
European muscle MRI study in limb girdle muscular dystrophy type R1/2A (LGMDR1/LGMD2A)Andrea Barp, Pascal Laforet, Luca Bello, et al.Revue Neurologique|September 7, 2015
Myofibrillar myopathies: State of the art, present and future challengesA Béhin, E Salort-Campana, K Wahbi, et al.American Journal of Medical Genetics. Part A|March 15, 2019
CHRNG-related nonlethal multiple pterygium syndrome: Muscle imaging pattern and clinical, histopathological, and molecular genetic findingsLaura Carrera-García, Daniel Natera-de Benito, Klaus Dieterich, et al.Muscle & Nerve|April 7, 2018
Clinical and imaging hallmarks of the MYH7-related myopathy with severe axial involvementIvana Dabaj, Robert Y Carlier, David Gómez-Andrés, et al.Journal of Neurology|September 24, 2021
Diagnostic interest of whole-body MRI in early- and late-onset LAMA2 muscular dystrophies: a large international cohortSusana Quijano-Roy, Jana Haberlova, Claudia Castiglioni, et al.Annals of Clinical and Translational Neurology|December 31, 2025
Whole-Body Pattern of Muscle Degeneration and Progression in SarcoglycanopathiesLaura Costa-Comellas, Mauro Monforte, Angel Sanchez-Montañez, et al.Pageof 18