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Journal of the American College of Radiology : JACR|November 27, 2022
ACR Appropriateness Criteria® Ataxia-Child, Rupa Radhakrishnan, Lindsey A G Shea, et al.Journal of Inherited Metabolic Disease|February 22, 2026
Pharmacodynamics, Efficacy, and Safety of Intraputaminal Eladocagene Exuparvovec Administered to Pediatric Patients With Aromatic L-Amino Acid Decarboxylase Deficiency Using an MR-Compatible Cannula: 48 Weeks of Follow-UpDaniel J Curry, Phillip L Pearl, Scellig S D Stone, et al.Journal of Attention Disorders|October 16, 2007
Atomoxetine treatment of ADHD in children with comorbid Tourette syndromeThomas J Spencer, F Randy Sallee, Donald L Gilbert, et al.Behavior Research Methods|November 9, 2021
OSARI, an Open-Source Anticipated Response Inhibition TaskJason L He, Rebecca J Hirst, Rohan Puri, et al.Neuromuscular Disorders : NMD|June 12, 2020
Randomized phase 2 trial and open-label extension of domagrozumab in Duchenne muscular dystrophyKathryn R Wagner, Hoda Z Abdel-Hamid, Jean K Mah, et al.Journal of Neuromuscular Diseases|June 14, 2021
A Randomized, Double-Blind, Placebo-Controlled, Global Phase 3 Study of Edasalonexent in Pediatric Patients with Duchenne Muscular Dystrophy: Results of the PolarisDMD TrialRichard S Finkel, Craig M McDonald, H Lee Sweeney, et al.Biological Psychiatry|December 16, 2011
Rare copy number variants in tourette syndrome disrupt genes in histaminergic pathways and overlap with autismThomas V Fernandez, Stephan J Sanders, Ilana R Yurkiewicz, et al.Pediatrics|November 20, 2025
Evaluation, Diagnosis, and Treatment of Sydenham Chorea: Consensus GuidelinesTerrence Thomas, Michael Eyre, Emanuela Ferrarin, et al.Journal of Neuromuscular Diseases|July 13, 2026
Navigating sexual health, fertility, and adult wellness in individuals with Duchenne muscular dystrophy: Current standards of care and future directionsNat Nasomyont, Amanda Appel, Susan Apkon, et al.Annals of Clinical and Translational Neurology|February 9, 2025
Clinical characterization of Collagen XII-related disease caused by biallelic COL12A1 variantsRiley M McCarty, Dimah Saade, Pinki Munot, et al.Pageof 21