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Journal of Neurology, Neurosurgery, and Psychiatry|February 27, 2026
Respiratory function in Becker muscular dystrophy: a comprehensive longitudinal studyPietro Riguzzi, Emma Grover, Marianela Schiava, et al.Journal of Neurology|June 7, 2025
Characterisation of a large, single-centre cohort of patients with Becker muscular dystrophy to inform standardised care guidelinesPietro Riguzzi, Holly Borland, Meredith K James, et al.JAMA Network Open|May 31, 2023
Effect of Perioperative Palliative Care on Health-Related Quality of Life Among Patients Undergoing Surgery for Cancer: A Randomized Clinical TrialRebecca A Aslakson, Elizabeth Rickerson, Bridget Fahy, et al.Muscle & Nerve|February 18, 2022
Cardiac and pulmonary findings in dysferlinopathy: A 3-year, longitudinal studyUrsula Moore, Roberto Fernandez-Torron, Marni Jacobs, et al.Neurology. Genetics|September 8, 2016
The Clinical Outcome Study for dysferlinopathy: An international multicenter studyElizabeth Harris, Catherine L Bladen, Anna Mayhew, et al.Human Mutation|April 23, 2013
ANO5 gene analysis in a large cohort of patients with anoctaminopathy: confirmation of male prevalence and high occurrence of the common exon 5 gene mutationAnna Sarkozy, Debbie Hicks, Judith Hudson, et al.Annals of Neurology|April 26, 2018
Congenital Titinopathy: Comprehensive characterization and pathogenic insightsEmily C Oates, Kristi J Jones, Sandra Donkervoort, et al.Nature Genetics|March 1, 2024
Digenic inheritance involving a muscle-specific protein kinase and the giant titin protein causes a skeletal muscle myopathyAna Töpf, Dan Cox, Irina T Zaharieva, et al.Cell|May 7, 2026
Multi-cohort proteogenomic analyses reveal genetic effects across the proteome and diseasomeMine Koprulu, Karl Smith-Byrne, Brian Richard Ferolito, et al.Nature Communications|January 27, 2022
National identity predicts public health support during a global pandemicJay J Van Bavel, Aleksandra Cichocka, Valerio Capraro, et al.Pageof 34