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Muscle & Nerve
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April 18, 2019
Intermittent glucocorticoid regimes for younger boys with duchenne muscular dystrophy: Balancing efficacy with side effects
Hugh 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 disorders
Hugh J McMillan
Muscle & Nerve
|
October 11, 2019
Nusinersen: Evidence of sustained clinical improvement and lessened fatigue in older ambulatory patients with spinal muscular atrophy
Hugh J McMillan
CMAJ : Canadian Medical Association Journal = Journal De L'Association Medicale Canadienne
|
October 18, 2017
We need a "made in Canada" orphan drug framework
Hugh J McMillan, Craig Campbell
Muscle & Nerve
|
June 2, 2021
Biomarkers in Duchenne and Becker muscular dystrophies
Hugh J McMillan, Hanns Lochmüller
Muscle & Nerve
|
November 16, 2023
Sustained clinical benefit following systemic gene replacement therapy in Duchenne muscular dystrophy
Hugh 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 testing
Srinivas Bulusu, Hugh J McMillan
Neurology
|
May 26, 2026
Predicting Functional Decline in Duchenne Muscular Dystrophy: Advancing Trial Readiness and Patient Counseling
Hugh J McMillan, Maryam Oskoui
Pediatric Radiology
|
October 14, 2010
Cranial nerve hypertrophy in pediatric chronic inflammatory demyelinating polyradiculoneuropathy
Hugh J McMillan, Elka Miller
Clinical Journal of Gastroenterology
|
July 21, 2015
Achalasia, chronic sensory neuropathy, and N-type calcium channel autoantibodies: beneficial response to IVIG
Hugh J McMillan, Jayashri Srinivasan
Page
of 14
Search research articles
Search
Showing results (1-10 of 134) with videos related to
Sort By:
Page
of 14
Muscle & Nerve
|
April 18, 2019
Intermittent glucocorticoid regimes for younger boys with duchenne muscular dystrophy: Balancing efficacy with side effects
Hugh 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 disorders
Hugh J McMillan
Muscle & Nerve
|
October 11, 2019
Nusinersen: Evidence of sustained clinical improvement and lessened fatigue in older ambulatory patients with spinal muscular atrophy
Hugh J McMillan
CMAJ : Canadian Medical Association Journal = Journal De L'Association Medicale Canadienne
|
October 18, 2017
We need a "made in Canada" orphan drug framework
Hugh J McMillan, Craig Campbell
Muscle & Nerve
|
June 2, 2021
Biomarkers in Duchenne and Becker muscular dystrophies
Hugh J McMillan, Hanns Lochmüller
Muscle & Nerve
|
November 16, 2023
Sustained clinical benefit following systemic gene replacement therapy in Duchenne muscular dystrophy
Hugh 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 testing
Srinivas Bulusu, Hugh J McMillan
Neurology
|
May 26, 2026
Predicting Functional Decline in Duchenne Muscular Dystrophy: Advancing Trial Readiness and Patient Counseling
Hugh J McMillan, Maryam Oskoui
Pediatric Radiology
|
October 14, 2010
Cranial nerve hypertrophy in pediatric chronic inflammatory demyelinating polyradiculoneuropathy
Hugh J McMillan, Elka Miller
Clinical Journal of Gastroenterology
|
July 21, 2015
Achalasia, chronic sensory neuropathy, and N-type calcium channel autoantibodies: beneficial response to IVIG
Hugh J McMillan, Jayashri Srinivasan
Page
of 14