Showing results (181-190 of 245) with videos related to

Sort By:
Pageof 25
European Journal of Neurology|June 1, 2021
Genotype-phenotype correlation in French patients with myelin protein zero gene-related inherited neuropathyMarie Subréville, Nathalie Bonello-Palot, Douniazed Yahiaoui, et al.
Neuromuscular Disorders : NMD|March 27, 2023
Expanding the muscle imaging spectrum in dysferlinopathy: description of an outlier population from the classical MRI patternLaura Llansó, Ursula Moore, Carla Bolano-Diaz, et al.
Neurology|April 14, 2019
FSHD1 and FSHD2 form a disease continuumSabrina Sacconi, Audrey Briand-Suleau, Marilyn Gros, et al.
Neurology|February 11, 2021
Impact of Coronavirus Disease 2019 in a French Cohort of Myasthenia GravisGuilhem Solé, Stéphane Mathis, Diane Friedman, et al.
Orphanet Journal of Rare Diseases|January 24, 2024
Multidisciplinary team meetings in treatment of spinal muscular atrophy adult patients: a real-life observatory for innovative treatmentsEmmanuelle Salort-Campana, Guilhem Solé, Armelle Magot, et al.
Neuromuscular Disorders : NMD|January 23, 2023
Myostatin and follistatin as monitoring and prognostic biomarkers in dysferlinopathyUrsula Moore, Esther Fernández-Simón, Marianela Schiava, et al.
Frontiers in Neurology|January 4, 2021
Intensive Teenage Activity Is Associated With Greater Muscle Hyperintensity on T1W Magnetic Resonance Imaging in Adults With DysferlinopathyUrsula Moore, Marni Jacobs, Roberto Fernandez-Torron, et al.
Journal of Cachexia, Sarcopenia and Muscle|April 4, 2022
Three-year quantitative magnetic resonance imaging and phosphorus magnetic resonance spectroscopy study in lower limb muscle in dysferlinopathyHarmen Reyngoudt, Fiona E Smith, Ericky Caldas de Almeida Araújo, et al.
Neuromuscular Disorders : NMD|February 21, 2021
Miyoshi myopathy and limb girdle muscular dystrophy R2 are the same diseaseUrsula Moore, Heather Gordish, Jordi Diaz-Manera, et al.
European Journal of Neurology|February 13, 2025
Disease Progression in Charcot-Marie-Tooth Disease Type 4B (CMT4B) Associated With Mutations in Myotubularin-Related Proteins 2 and 13Alessandro Bertini, Mary M Reilly, Chiara Pisciotta, et al.
Pageof 25