Ian R. Woodcock
Melbourne, VIC, Australia
Last Updated: 09/26/2026
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Found 28 publications
Strategic consensus on the clinical translation of advanced therapies in paediatric rare neurological disorders.
Journal: Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics
Published: February 05, 2026
Author Correction: Intrathecal onasemnogene abeparvovec for treatment-experienced patients with spinal muscular atrophy: a phase 3b, open-label trial.
Journal: Nature medicine
Published: January 28, 2026
Framing childhood-onset facioscapulohumeral dystrophy: from first symptoms to future trials.
Journal: Neuromuscular disorders : NMD
Published: January 11, 2026
A Retrospective Cohort Study of Nutrition Outcomes in Children With Spinal Muscular Atrophy Type 1 and 2 Treated With Disease Modifying Therapies.
Journal: Muscle & nerve
Published: September 17, 2025
Intrathecal onasemnogene abeparvovec for treatment-experienced patients with spinal muscular atrophy: a phase 3b, open-label trial.
Journal: Nature medicine
Published: July 23, 2025
Detailed immune cell profiling of paediatric patient with limb girdle muscular dystrophy R3.
Journal: Journal of the neurological sciences
Published: March 16, 2025
Cost-Effectiveness of Newborn Screening for Spinal Muscular Atrophy in Australian Hospitals.
Journal: Neurology and therapy
Published: February 21, 2025
Survival in Duchenne muscular dystrophy in Australia: a 50 year retrospective cohort study.
Journal: The Lancet regional health. Western Pacific
Published: December 15, 2024
Effect of creatine monohydrate on motor function in children with facioscapulohumeral muscular dystrophy: A multicenter, randomized, double-blind placebo-controlled crossover trial.
Journal: Pharmacotherapy
Published: November 02, 2024
A contemporary analysis of the Australian clinical and genetic landscape of spinal muscular atrophy: a registry based study.
Journal: The Lancet regional health. Western Pacific
Published: April 07, 2024
Nutrition outcomes of disease modifying therapies in spinal muscular atrophy: A systematic review.
Journal: Muscle & nerve
Published: March 06, 2024
Rare homozygous disease-associated sequence variants in children with spinal muscular atrophy: a phenotypic description and review of the literature.
Journal: Neuromuscular disorders : NMD
Published: December 03, 2023
Last Updated: 09/26/2026