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Nicholas A Di Prospero

Showing results (21-30 of 27) with videos related to

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The Journal of Clinical Investigation|February 24, 2007
Trichostatin A increases SMN expression and survival in a mouse model of spinal muscular atrophyAmy M Avila, Barrington G Burnett, Addis A Taye, et al.
Plos Genetics|January 22, 2010
Altered gene expression and DNA damage in peripheral blood cells from Friedreich's ataxia patients: cellular model of pathologyAstrid C Haugen, Nicholas A Di Prospero, Joel S Parker, et al.
International Journal of Clinical Pharmacology and Therapeutics|November 20, 2014
Effects of rifampin, cyclosporine A, and probenecid on the pharmacokinetic profile of canagliflozin, a sodium glucose co-transporter 2 inhibitor, in healthy participantsDamayanthi Devineni, Nicole Vaccaro, Joe Murphy, et al.
Alimentary Pharmacology & Therapeutics|March 15, 2023
Review article: The need for more efficient and patient-oriented drug development pathways in NASH-setting the scene for platform trialsJuan M Pericàs, Nicholas A Di Prospero, Quentin M Anstee, et al.
Brain : a Journal of Neurology|October 23, 2009
Clinical features of spinal and bulbar muscular atrophyLindsay E Rhodes, Brandi K Freeman, Sungyoung Auh, et al.
Rehabilitation Research and Practice|May 31, 2014
Assessing function and endurance in adults with spinal and bulbar muscular atrophy: validity of the adult myopathy assessment toolMichael O Harris-Love, Lindsay Fernandez-Rhodes, Galen Joe, et al.
The Lancet. Neurology|January 11, 2011
Efficacy and safety of dutasteride in patients with spinal and bulbar muscular atrophy: a randomised placebo-controlled trialLindsay E Fernández-Rhodes, Angela D Kokkinis, Michelle J White, et al.
Pageof 3

Showing results (21-30 of 27) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 27 results.
The Journal of Clinical Investigation|February 24, 2007
Trichostatin A increases SMN expression and survival in a mouse model of spinal muscular atrophyAmy M Avila, Barrington G Burnett, Addis A Taye, et al.
Plos Genetics|January 22, 2010
Altered gene expression and DNA damage in peripheral blood cells from Friedreich's ataxia patients: cellular model of pathologyAstrid C Haugen, Nicholas A Di Prospero, Joel S Parker, et al.
International Journal of Clinical Pharmacology and Therapeutics|November 20, 2014
Effects of rifampin, cyclosporine A, and probenecid on the pharmacokinetic profile of canagliflozin, a sodium glucose co-transporter 2 inhibitor, in healthy participantsDamayanthi Devineni, Nicole Vaccaro, Joe Murphy, et al.
Alimentary Pharmacology & Therapeutics|March 15, 2023
Review article: The need for more efficient and patient-oriented drug development pathways in NASH-setting the scene for platform trialsJuan M Pericàs, Nicholas A Di Prospero, Quentin M Anstee, et al.
Brain : a Journal of Neurology|October 23, 2009
Clinical features of spinal and bulbar muscular atrophyLindsay E Rhodes, Brandi K Freeman, Sungyoung Auh, et al.
Rehabilitation Research and Practice|May 31, 2014
Assessing function and endurance in adults with spinal and bulbar muscular atrophy: validity of the adult myopathy assessment toolMichael O Harris-Love, Lindsay Fernandez-Rhodes, Galen Joe, et al.
The Lancet. Neurology|January 11, 2011
Efficacy and safety of dutasteride in patients with spinal and bulbar muscular atrophy: a randomised placebo-controlled trialLindsay E Fernández-Rhodes, Angela D Kokkinis, Michelle J White, et al.
Pageof 3