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Spine
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February 4, 2011
The natural history of cardiac and pulmonary function decline in patients with duchenne muscular dystrophy
Rolando Roberto, Anto Fritz, Yolanda Hagar, et al.
Minerva Anestesiologica
|
April 8, 2016
Is high-dose β-lactam therapy associated with excessive drug toxicity in critically ill patients?
Craig McDonald, Menino O Cotta, Peter J Little, et al.
Gait & Posture
|
December 18, 2022
Kinematic changes in gait in boys with Duchenne Muscular Dystrophy: Utility of the Gait Deviation Index, the Gait Profile Score and the Gait Variable Scores
Susan Sienko, Cathleen Buckon, Anita Bagley, et al.
Muscle & Nerve
|
December 28, 2007
Variable phenotypes associated with mutations in DOK7
Jennifer A Anderson, Jarae J Ng, Constance Bowe, et al.
Frontiers in Neural Circuits
|
November 3, 2018
Functional Neuronal Topography: A Statistical Approach to Micro Mapping Neuronal Location
Angela Jacques, Alison Wright, Nicholas Chaaya, et al.
Gait & Posture
|
September 26, 2021
Longitudinal changes in energy cost during walking in boys with Duchenne Muscular Dystrophy (DMD)
Susan Sienko, Cathleen E Buckon, Anita Bagley, et al.
Journal of Neuromuscular Diseases
|
November 1, 2021
Knee Strength and Ankle Range of Motion Impacts on Timed Function Tests in Duchenne Muscular Dystrophy: In the Era of Glucocorticoids
Tina Duong, Jennifer Canbek, Alicia Fernandez-Fernandez, et al.
The Journal of Spinal Cord Medicine
|
October 27, 2004
Timed motor test for wheelchair users: initial development and application in children with spinal cord injury
Ross Chafetz, Craig McDonald, M J Mulcahey, et al.
Journal of Neuromuscular Diseases
|
February 16, 2024
Draft Guidance for Industry Duchenne Muscular Dystrophy, Becker Muscular Dystrophy, and Related Dystrophinopathies - Developing Potential Treatments for the Entire Spectrum of Disease
Craig McDonald, Eric Camino, Rafael Escandon, et al.
Orphanet Journal of Rare Diseases
|
June 25, 2015
How a patient advocacy group developed the first proposed draft guidance document for industry for submission to the U.S. Food and Drug Administration
Pat Furlong, John F P Bridges, Lawrence Charnas, et al.
Page
of 5
Search research articles
Search
Showing results (11-20 of 47) with videos related to
Sort By:
Page
of 5
Spine
|
February 4, 2011
The natural history of cardiac and pulmonary function decline in patients with duchenne muscular dystrophy
Rolando Roberto, Anto Fritz, Yolanda Hagar, et al.
Minerva Anestesiologica
|
April 8, 2016
Is high-dose β-lactam therapy associated with excessive drug toxicity in critically ill patients?
Craig McDonald, Menino O Cotta, Peter J Little, et al.
Gait & Posture
|
December 18, 2022
Kinematic changes in gait in boys with Duchenne Muscular Dystrophy: Utility of the Gait Deviation Index, the Gait Profile Score and the Gait Variable Scores
Susan Sienko, Cathleen Buckon, Anita Bagley, et al.
Muscle & Nerve
|
December 28, 2007
Variable phenotypes associated with mutations in DOK7
Jennifer A Anderson, Jarae J Ng, Constance Bowe, et al.
Frontiers in Neural Circuits
|
November 3, 2018
Functional Neuronal Topography: A Statistical Approach to Micro Mapping Neuronal Location
Angela Jacques, Alison Wright, Nicholas Chaaya, et al.
Gait & Posture
|
September 26, 2021
Longitudinal changes in energy cost during walking in boys with Duchenne Muscular Dystrophy (DMD)
Susan Sienko, Cathleen E Buckon, Anita Bagley, et al.
Journal of Neuromuscular Diseases
|
November 1, 2021
Knee Strength and Ankle Range of Motion Impacts on Timed Function Tests in Duchenne Muscular Dystrophy: In the Era of Glucocorticoids
Tina Duong, Jennifer Canbek, Alicia Fernandez-Fernandez, et al.
The Journal of Spinal Cord Medicine
|
October 27, 2004
Timed motor test for wheelchair users: initial development and application in children with spinal cord injury
Ross Chafetz, Craig McDonald, M J Mulcahey, et al.
Journal of Neuromuscular Diseases
|
February 16, 2024
Draft Guidance for Industry Duchenne Muscular Dystrophy, Becker Muscular Dystrophy, and Related Dystrophinopathies - Developing Potential Treatments for the Entire Spectrum of Disease
Craig McDonald, Eric Camino, Rafael Escandon, et al.
Orphanet Journal of Rare Diseases
|
June 25, 2015
How a patient advocacy group developed the first proposed draft guidance document for industry for submission to the U.S. Food and Drug Administration
Pat Furlong, John F P Bridges, Lawrence Charnas, et al.
Page
of 5