Showing results (591-600 of 831) with videos related to
Sort By:
Pageof 84
Journal of Neurology|August 31, 2006
Comparison of CMT1A and CMT2: similarities and differencesHenriette M E Bienfait, Camiel Verhamme, Ivo N van Schaik, et al.Ultrasound in Medicine & Biology|December 17, 2008
Skeletal muscle ultrasound: correlation between fibrous tissue and echo intensitySigrid Pillen, Ramon O Tak, Machiel J Zwarts, et al.Disability and Rehabilitation|May 18, 2026
Congenital myopathies in adult patients: lived experiences and coping mechanismsLizan Stinissen, Erin Peet, Sanne A J H van de Camp, et al.International Journal of Molecular Sciences|August 27, 2020
Age-Associated Salivary MicroRNA Biomarkers for Oculopharyngeal Muscular DystrophyVered Raz, Rosemarie H M J M Kroon, Hailiang Mei, et al.Journal of Neuromuscular Diseases|August 23, 2024
Cardiac Involvement in LAMA2-Related Muscular Dystrophy and SELENON-Related Congenital Myopathy: A Case SeriesKarlijn Bouman, Frederik M A van den Heuvel, Reinder Evertz, et al.Scientific Reports|January 27, 2022
Facioscapulohumeral dystrophy transcriptome signatures correlate with different stages of disease and are marked by different MRI biomarkersAnita van den Heuvel, Saskia Lassche, Karlien Mul, et al.European Journal of Nuclear Medicine|January 1, 1985
The elimination rate of 123I-heptadecanoic acid after intracoronary and intravenous administrationF C Visser, M J van Eenige, E E van der Wall, et al.Neuromuscular Disorders : NMD|April 19, 2017
Respiratory function in facioscapulohumeral muscular dystrophy 1M Wohlgemuth, C G C Horlings, E L van der Kooi, et al.Neurology|October 22, 2021
Natural History of Facioscapulohumeral Dystrophy in Children: A 2-Year Follow-upJildou N Dijkstra, Rianne J M Goselink, Nens van Alfen, et al.Neuromuscular Disorders : NMD|June 19, 2012
Brody syndrome: a clinically heterogeneous entity distinct from Brody disease: a review of literature and a cross-sectional clinical study in 17 patientsN C Voermans, A E Laan, A Oosterhof, et al.Pageof 84