Hugh J. Mcmillan

401 Smyth Road
Ottawa, ON, Canada

Last Updated: 09/26/2026

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Found 145 publications

Total body and appendicular lean mass by dual-energy X-ray absorptiometry are highly associated with muscle function and bone mineral density in Becker muscular dystrophy.

Total body and appendicular lean mass by dual-energy X-ray absorptiometry are highly associated with muscle function and bone mineral density in Becker muscular dystrophy.

Journal: Journal of neuromuscular diseases

Published: August 28, 2026

Expanding Vamorolone Treatment Access for Canadians with Duchenne Muscular Dystrophy.

Expanding Vamorolone Treatment Access for Canadians with Duchenne Muscular Dystrophy.

Journal: The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques

Published: July 13, 2026

Navigating sexual health, fertility, and adult wellness in individuals with Duchenne muscular dystrophy: Current standards of care and future directions.

Navigating sexual health, fertility, and adult wellness in individuals with Duchenne muscular dystrophy: Current standards of care and future directions.

Journal: Journal of neuromuscular diseases

Published: July 13, 2026

Mobile robotic walker enables precision moderately intense exercise and environmental exploration in a child with cerebral palsy GMFCS IV: assessment of use, user experience and quantitative impact in a home and hospital based setting.

Mobile robotic walker enables precision moderately intense exercise and environmental exploration in a child with cerebral palsy GMFCS IV: assessment of use, user experience and quantitative impact in a home and hospital based setting.

Journal: Disability and rehabilitation. Assistive technology

Published: July 09, 2026

Predicting Functional Decline in Duchenne Muscular Dystrophy: Advancing Trial Readiness and Patient Counseling.

Predicting Functional Decline in Duchenne Muscular Dystrophy: Advancing Trial Readiness and Patient Counseling.

Journal: Neurology

Published: May 26, 2026

Maternal-Fetal Administration of Risdiplam Partially Rescues the SMNΔ7 Mouse Model of Spinal Muscular Atrophy.

Maternal-Fetal Administration of Risdiplam Partially Rescues the SMNΔ7 Mouse Model of Spinal Muscular Atrophy.

Journal: Annals of neurology

Published: April 23, 2026

Onasemnogene abeparvovec gene therapy for treatment of patients with spinal muscular atrophy: Updated real-world practical considerations.

Onasemnogene abeparvovec gene therapy for treatment of patients with spinal muscular atrophy: Updated real-world practical considerations.

Journal: Journal of neuromuscular diseases

Published: November 10, 2025

Extracellular vesicles as biomarkers of disease progression and therapeutic response in patients with spinal muscular atrophy.

Extracellular vesicles as biomarkers of disease progression and therapeutic response in patients with spinal muscular atrophy.

Journal: Molecular therapy. Advances

Published: September 26, 2025

Assessing biomarkers of bone metabolism and the role of the interleukin-6 signaling pathway in patients with Duchenne muscular dystrophy.

Assessing biomarkers of bone metabolism and the role of the interleukin-6 signaling pathway in patients with Duchenne muscular dystrophy.

Journal: Neuromuscular disorders : NMD

Published: September 09, 2025

Optimizing Care for Growth and Puberty in Duchenne Muscular Dystrophy: A Survey of Clinical Practice in the OPTIMIZE DMD Consortium.

Optimizing Care for Growth and Puberty in Duchenne Muscular Dystrophy: A Survey of Clinical Practice in the OPTIMIZE DMD Consortium.

Journal: Muscle & nerve

Published: September 04, 2025

Bullying experiences of youth with neuromuscular disorders and their well-being: A survey study.

Bullying experiences of youth with neuromuscular disorders and their well-being: A survey study.

Journal: Journal of neuromuscular diseases

Published: August 25, 2025

Financial Toxicity and Its Determinants in Individuals Living With Inherited and Acquired Neuromuscular Disorders: The BIND Study.

Financial Toxicity and Its Determinants in Individuals Living With Inherited and Acquired Neuromuscular Disorders: The BIND Study.

Journal: Neurology

Published: August 20, 2025

Showing 1-12 of 145

Last Updated: 09/26/2026