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Hugh J McMillan

Showing results (1-10 of 134) with videos related to

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Muscle & Nerve|April 18, 2019
Intermittent glucocorticoid regimes for younger boys with duchenne muscular dystrophy: Balancing efficacy with side effectsHugh J McMillan
Muscle & Nerve|April 23, 2015
Congenital muscular dystrophies: New evidence-based guidelines for the diagnosis and management of this evolving group of muscle disordersHugh J McMillan
Muscle & Nerve|October 11, 2019
Nusinersen: Evidence of sustained clinical improvement and lessened fatigue in older ambulatory patients with spinal muscular atrophyHugh J McMillan
CMAJ : Canadian Medical Association Journal = Journal De L'Association Medicale Canadienne|October 18, 2017
We need a "made in Canada" orphan drug frameworkHugh J McMillan, Craig Campbell
Muscle & Nerve|June 2, 2021
Biomarkers in Duchenne and Becker muscular dystrophiesHugh J McMillan, Hanns Lochmüller
Muscle & Nerve|November 16, 2023
Sustained clinical benefit following systemic gene replacement therapy in Duchenne muscular dystrophyHugh J McMillan, Hanns Lochmüller
American Journal of Electroneurodiagnostic Technology|October 13, 2011
A report of hereditary neuropathy with liability to pressure palsy (HNPP) presenting with brachial plexopathy: the value of complete electrodiagnostic testingSrinivas Bulusu, Hugh J McMillan
Neurology|May 26, 2026
Predicting Functional Decline in Duchenne Muscular Dystrophy: Advancing Trial Readiness and Patient CounselingHugh J McMillan, Maryam Oskoui
Pediatric Radiology|October 14, 2010
Cranial nerve hypertrophy in pediatric chronic inflammatory demyelinating polyradiculoneuropathyHugh J McMillan, Elka Miller
Clinical Journal of Gastroenterology|July 21, 2015
Achalasia, chronic sensory neuropathy, and N-type calcium channel autoantibodies: beneficial response to IVIGHugh J McMillan, Jayashri Srinivasan
Pageof 14

Showing results (1-10 of 134) with videos related to

Sort By:
Pageof 14
Muscle & Nerve|April 18, 2019
Intermittent glucocorticoid regimes for younger boys with duchenne muscular dystrophy: Balancing efficacy with side effectsHugh J McMillan
Muscle & Nerve|April 23, 2015
Congenital muscular dystrophies: New evidence-based guidelines for the diagnosis and management of this evolving group of muscle disordersHugh J McMillan
Muscle & Nerve|October 11, 2019
Nusinersen: Evidence of sustained clinical improvement and lessened fatigue in older ambulatory patients with spinal muscular atrophyHugh J McMillan
CMAJ : Canadian Medical Association Journal = Journal De L'Association Medicale Canadienne|October 18, 2017
We need a "made in Canada" orphan drug frameworkHugh J McMillan, Craig Campbell
Muscle & Nerve|June 2, 2021
Biomarkers in Duchenne and Becker muscular dystrophiesHugh J McMillan, Hanns Lochmüller
Muscle & Nerve|November 16, 2023
Sustained clinical benefit following systemic gene replacement therapy in Duchenne muscular dystrophyHugh J McMillan, Hanns Lochmüller
American Journal of Electroneurodiagnostic Technology|October 13, 2011
A report of hereditary neuropathy with liability to pressure palsy (HNPP) presenting with brachial plexopathy: the value of complete electrodiagnostic testingSrinivas Bulusu, Hugh J McMillan
Neurology|May 26, 2026
Predicting Functional Decline in Duchenne Muscular Dystrophy: Advancing Trial Readiness and Patient CounselingHugh J McMillan, Maryam Oskoui
Pediatric Radiology|October 14, 2010
Cranial nerve hypertrophy in pediatric chronic inflammatory demyelinating polyradiculoneuropathyHugh J McMillan, Elka Miller
Clinical Journal of Gastroenterology|July 21, 2015
Achalasia, chronic sensory neuropathy, and N-type calcium channel autoantibodies: beneficial response to IVIGHugh J McMillan, Jayashri Srinivasan
Pageof 14