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Molecular Genetics & Genomic Medicine
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September 7, 2019
A novel TTN deletion in a family with skeletal myopathy, facial weakness, and dilated cardiomyopathy
Jennifer Roggenbuck, Kelly Rich, Ana Morales, et al.
The EPMA Journal
|
March 7, 2020
Evaluation of machine learning methodology for the prediction of healthcare resource utilization and healthcare costs in patients with critical limb ischemia-is preventive and personalized approach on the horizon?
Jeffrey S Berger, Lloyd Haskell, Windsor Ting, et al.
Research Square
|
April 8, 2025
Targeting senescence in Amyotrophic Lateral Sclerosis: senolytic treatment improves neuromuscular function and preserves cortical excitability in a TDP-43<sup>Q331K</sup> mouse model
Jose A Viteri, Nathan R Kerr, Charles D Brennan, et al.
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics
|
June 14, 2024
MeCP2 gene therapy ameliorates disease phenotype in mouse model for Pitt Hopkins syndrome
Cassandra N Dennys, Sheryl Anne D Vermudez, Robert J M Deacon, et al.
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of 1
Search research articles
Search
Showing results (1-10 of 4) with videos related to
Sort By:
Page
of 1
Molecular Genetics & Genomic Medicine
|
September 7, 2019
A novel TTN deletion in a family with skeletal myopathy, facial weakness, and dilated cardiomyopathy
Jennifer Roggenbuck, Kelly Rich, Ana Morales, et al.
The EPMA Journal
|
March 7, 2020
Evaluation of machine learning methodology for the prediction of healthcare resource utilization and healthcare costs in patients with critical limb ischemia-is preventive and personalized approach on the horizon?
Jeffrey S Berger, Lloyd Haskell, Windsor Ting, et al.
Research Square
|
April 8, 2025
Targeting senescence in Amyotrophic Lateral Sclerosis: senolytic treatment improves neuromuscular function and preserves cortical excitability in a TDP-43<sup>Q331K</sup> mouse model
Jose A Viteri, Nathan R Kerr, Charles D Brennan, et al.
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics
|
June 14, 2024
MeCP2 gene therapy ameliorates disease phenotype in mouse model for Pitt Hopkins syndrome
Cassandra N Dennys, Sheryl Anne D Vermudez, Robert J M Deacon, et al.
Page
of 1