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Scientific Reports|November 6, 2022
Dual-energy X-ray absorptiometry measures of lean body mass as a biomarker for progression in boys with Duchenne muscular dystrophySarah P Sherlock, Jeffrey Palmer, Kathryn R Wagner, et al.
Food & Function|April 2, 2024
Theabrownin from Fu Brick tea ameliorates high-fat induced insulin resistance, hepatic steatosis, and inflammation in mice by altering the composition and metabolites of gut microbiotaZhongting Lu, Yan Zheng, Juan Zheng, et al.
Neurology. Clinical Practice|November 22, 2019
Consensus-based care recommendations for congenital and childhood-onset myotonic dystrophy type 1Nicholas E Johnson, Eugenio Zapata Aldana, Nathalie Angeard, et al.
Neurology|January 16, 2020
MRI vastus lateralis fat fraction predicts loss of ambulation in Duchenne muscular dystrophyKarin J Naarding, Harmen Reyngoudt, Erik W van Zwet, et al.
Frontiers in Cell and Developmental Biology|March 30, 2022
Desmin Modulates Muscle Cell Adhesion and MigrationCoralie Hakibilen, Florence Delort, Marie-Thérèse Daher, et al.
The Journal of Pediatrics|April 9, 2019
Comparison of Pulmonary Function Decline in Steroid-Treated and Steroid-Naïve Patients with Duchenne Muscular DystrophyHemant Sawnani, Paul S Horn, Brenda Wong, et al.
Neurology. Clinical Practice|June 25, 2024
Spinal Muscular Atrophy Update in Best Practices: Recommendations for Diagnosis ConsiderationsMary Schroth, Jennifer Deans, Kapil Arya, et al.
Neuromuscular Disorders : NMD|April 9, 2022
Real-world and natural history data for drug evaluation in Duchenne muscular dystrophy: suitability of the North Star Ambulatory Assessment for comparisons with external controlsFrancesco Muntoni, James Signorovitch, Gautam Sajeev, et al.
Journal of Neurology|April 9, 2022
Quantitative magnetic resonance imaging measures as biomarkers of disease progression in boys with Duchenne muscular dystrophy: a phase 2 trial of domagrozumabSarah P Sherlock, Jeffrey Palmer, Kathryn R Wagner, et al.
Plos One|July 10, 2024
Meaningful changes in motor function in Duchenne muscular dystrophy (DMD): A multi-center studyFrancesco Muntoni, James Signorovitch, Gautam Sajeev, et al.
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