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Journal of Child Neurology|January 16, 2019
Parents' Experiences of Information and Decision Making in the Care of Their Child With Severe Spinal Muscular Atrophy: A Population SurveyKim Beernaert, Malin Lövgren, Jørgen Jeppesen, et al.Acta Neuropathologica|November 1, 2002
Cytoskeletal derangements in hereditary myopathy with a desmin L345P mutationLena Carlsson, Christine Fischer, Gunnnar Sjöberg, et al.Journal of Child Neurology|December 7, 2018
Bereaved Parents More Satisfied With the Care Given to Their Child With Severe Spinal Muscular Atrophy Than NonbereavedElin Hjorth, Ulrika Kreicbergs, Thomas Sejersen, et al.Journal of Neuromuscular Diseases|July 4, 2026
Disease progression and economic burden of duchenne muscular dystrophy: A retrospective study using Swedish register dataThomas Sejersen, Anna-Karin Kroksmark, Aina Törnblom, et al.Neurorehabilitation|July 28, 2007
Sustained favorable effects of cognitive training in children with acquired brain injuriesIngrid van 't Hooft, Karin Andersson, Barbro Bergman, et al.Pharmacoeconomics|December 14, 2022
Caregiver Burden of Spinal Muscular Atrophy: A Systematic ReviewErik Landfeldt, Sophia Abner, Astrid Pechmann, et al.International Journal of Cardiology|November 17, 2007
Deletion in TNNI3 gene is associated with restrictive cardiomyopathyAnna Kostareva, Alexandra Gudkova, Gunnar Sjöberg, et al.Neurology|January 2, 2024
Bisphosphonates in Glucocorticoid-Treated Patients With Duchenne Muscular Dystrophy: A Systematic Review and Grading of the EvidenceErik Landfeldt, Kim Phung, Farasat Zaman, et al.Biochemistry and Biophysics Reports|January 19, 2026
Humanin improves bone health in a glucocorticoid-treated mouse model of Duchenne muscular dystrophyTherése Cedervall, Baptiste Jude, Ferdinand von Walden, et al.Biochimica Et Biophysica Acta. Molecular Basis of Disease|February 28, 2020
Desmin mutations result in mitochondrial dysfunction regardless of their aggregation propertiesNatalia Smolina, Aleksandr Khudiakov, Anastasiya Knyazeva, et al.Pageof 8