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Movement Disorders : Official Journal of the Movement Disorder Society|October 7, 2020
Low Prevalence of NOTCH2NLC GGC Repeat Expansion in White Patients with Movement DisordersWai Yan Yau, Jana Vandrovcova, Roisin Sullivan, et al.
Muscle & Nerve|October 21, 2017
Chronic pain has a strong impact on quality of life in facioscapulohumeral muscular dystrophyGermán Morís, Libby Wood, Roberto FernáNdez-Torrón, et al.
Journal of Neurology|April 12, 2017
The UK Myotonic Dystrophy Patient Registry: facilitating and accelerating clinical researchLibby Wood, Isabell Cordts, Antonio Atalaia, et al.
Health and Social Care Delivery Research|November 2, 2024
Using the Recommended Summary Plan for Emergency Care and Treatment in Primary Care: a mixed methods studyAnne-Marie Slowther, Jenny Harlock, Celia J Bernstein, et al.
Neuromuscular Disorders : NMD|September 29, 2019
Genetic and phenotypic characterisation of inherited myopathies in a tertiary neuromuscular centreEnrico Bugiardini, Alaa M Khan, Rahul Phadke, et al.
Molecular Therapy. Methods & Clinical Development|October 27, 2021
miR-223-3p and miR-24-3p as novel serum-based biomarkers for myotonic dystrophy type 1Demetris Koutalianos, Andrie Koutsoulidou, Chrystalla Mytidou, et al.
Mindfulness|March 19, 2026
The Evolution of an Indigenous Mindfulness Program: Qualitative Findings from the IndigenousMIND StudyJeffrey Proulx, Chelsea Cooley, Sojas Wagle, et al.
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