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Clinical Trials (London, England)
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July 2, 2019
Design and analysis of a clinical trial using previous trials as historical control
David Alan Schoenfeld, Dianne M Finkelstein, Eric Macklin, et al.
Neuromuscular Disorders : NMD
|
March 5, 2023
Urine titin as a novel biomarker for Duchenne muscular dystrophy
Misawa Niki Ishii, Masato Nakashima, Hidenori Kamiguchi, et al.
Annals of Clinical and Translational Neurology
|
November 16, 2016
Predicting disease progression in amyotrophic lateral sclerosis
Albert A Taylor, Christina Fournier, Meraida Polak, et al.
Health and Quality of Life Outcomes
|
January 22, 2022
Qualitative measures that assess functional disability and quality of life in ALS
Susan L Hartmaier, Thomas Rhodes, Suzanne F Cook, et al.
Skeletal Muscle
|
November 19, 2023
Electrical impedance myography detects dystrophin-related muscle changes in mdx mice
Tetsuaki Hiyoshi, Fuqiang Zhao, Rina Baba, et al.
Neurology
|
October 10, 2014
The PRO-ACT database: design, initial analyses, and predictive features
Nazem Atassi, James Berry, Amy Shui, et al.
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics
|
January 24, 2015
Being PRO-ACTive: What can a Clinical Trial Database Reveal About ALS?
Neta Zach, David L Ennist, Albert A Taylor, et al.
Molecular Neurobiology
|
October 19, 2018
Laquinimod Treatment Improves Myelination Deficits at the Transcriptional and Ultrastructural Levels in the YAC128 Mouse Model of Huntington Disease
Marta Garcia-Miralles, Nur Amirah Binte Mohammad Yusof, Jing Ying Tan, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration
|
January 21, 2021
ALSUntangled 59: Tamoxifen
Richard Bedlack, Sky Kihuwa-Mani, Paul E Barkhaus, et al.
Nature Biotechnology
|
November 3, 2014
Crowdsourced analysis of clinical trial data to predict amyotrophic lateral sclerosis progression
Robert Küffner, Neta Zach, Raquel Norel, et al.
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of 3
Search research articles
Search
Showing results (11-20 of 23) with videos related to
Sort By:
Page
of 3
Clinical Trials (London, England)
|
July 2, 2019
Design and analysis of a clinical trial using previous trials as historical control
David Alan Schoenfeld, Dianne M Finkelstein, Eric Macklin, et al.
Neuromuscular Disorders : NMD
|
March 5, 2023
Urine titin as a novel biomarker for Duchenne muscular dystrophy
Misawa Niki Ishii, Masato Nakashima, Hidenori Kamiguchi, et al.
Annals of Clinical and Translational Neurology
|
November 16, 2016
Predicting disease progression in amyotrophic lateral sclerosis
Albert A Taylor, Christina Fournier, Meraida Polak, et al.
Health and Quality of Life Outcomes
|
January 22, 2022
Qualitative measures that assess functional disability and quality of life in ALS
Susan L Hartmaier, Thomas Rhodes, Suzanne F Cook, et al.
Skeletal Muscle
|
November 19, 2023
Electrical impedance myography detects dystrophin-related muscle changes in mdx mice
Tetsuaki Hiyoshi, Fuqiang Zhao, Rina Baba, et al.
Neurology
|
October 10, 2014
The PRO-ACT database: design, initial analyses, and predictive features
Nazem Atassi, James Berry, Amy Shui, et al.
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics
|
January 24, 2015
Being PRO-ACTive: What can a Clinical Trial Database Reveal About ALS?
Neta Zach, David L Ennist, Albert A Taylor, et al.
Molecular Neurobiology
|
October 19, 2018
Laquinimod Treatment Improves Myelination Deficits at the Transcriptional and Ultrastructural Levels in the YAC128 Mouse Model of Huntington Disease
Marta Garcia-Miralles, Nur Amirah Binte Mohammad Yusof, Jing Ying Tan, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration
|
January 21, 2021
ALSUntangled 59: Tamoxifen
Richard Bedlack, Sky Kihuwa-Mani, Paul E Barkhaus, et al.
Nature Biotechnology
|
November 3, 2014
Crowdsourced analysis of clinical trial data to predict amyotrophic lateral sclerosis progression
Robert Küffner, Neta Zach, Raquel Norel, et al.
Page
of 3