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Craig Campbell

Showing results (121-130 of 188) with videos related to

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Neurology|February 15, 2024
Neurobehavioral Phenotype of Children With Congenital Myotonic DystrophyNamita Patel, Kiera N Berggren, Man Hung, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|April 19, 2022
Electronic alerts and a care bundle for acute kidney injury-an Australian cohort studySradha Kotwal, Sanjeeva Herath, Jonathan Erlich, et al.
The Journal of Continuing Education in the Health Professions|June 20, 2007
Developing an instrument to measure bias in CMEJatinder Takhar, Dave Dixon, Jill Donahue, et al.
Orphanet Journal of Rare Diseases|May 27, 2026
Implementation of a neuromuscular clinical trial network: a rare disease model for enhancing clinical trial readiness, capacity, and access in CanadaKerri Lynn Schellenberg, Homira Osman, Maria Masnata, et al.
Clinical Chemistry|April 28, 2023
Analytical and Non-Analytical Variation May Lead to Inappropriate Antimicrobial Dosing in Neonates: An In Silico StudyThi A Nguyen, Ranita Kirubakaran, Hayley B Schultz, et al.
Neurology|June 17, 2016
Disease burden and functional outcomes in congenital myotonic dystrophy: A cross-sectional studyNicholas E Johnson, Russell Butterfield, Kiera Berggren, et al.
Developmental Medicine and Child Neurology|October 30, 2015
Parent-reported multi-national study of the impact of congenital and childhood onset myotonic dystrophyNicholas E Johnson, Anne-Berit Ekstrom, Craig Campbell, et al.
Science (New York, N.Y.)|November 11, 2009
Pathogenesis of chytridiomycosis, a cause of catastrophic amphibian declinesJamie Voyles, Sam Young, Lee Berger, et al.
Journal of Comparative Effectiveness Research|October 25, 2021
Meta-analyses of deflazacort versus prednisone/prednisolone in patients with nonsense mutation Duchenne muscular dystrophyPerry B Shieh, Gary Elfring, Panayiota Trifillis, et al.
Muscle & Nerve|July 28, 2016
Myostatin inhibitor ACE-031 treatment of ambulatory boys with Duchenne muscular dystrophy: Results of a randomized, placebo-controlled clinical trialCraig Campbell, Hugh J McMillan, Jean K Mah, et al.
Pageof 19

Showing results (121-130 of 188) with videos related to

Sort By:
Pageof 19
Neurology|February 15, 2024
Neurobehavioral Phenotype of Children With Congenital Myotonic DystrophyNamita Patel, Kiera N Berggren, Man Hung, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|April 19, 2022
Electronic alerts and a care bundle for acute kidney injury-an Australian cohort studySradha Kotwal, Sanjeeva Herath, Jonathan Erlich, et al.
The Journal of Continuing Education in the Health Professions|June 20, 2007
Developing an instrument to measure bias in CMEJatinder Takhar, Dave Dixon, Jill Donahue, et al.
Orphanet Journal of Rare Diseases|May 27, 2026
Implementation of a neuromuscular clinical trial network: a rare disease model for enhancing clinical trial readiness, capacity, and access in CanadaKerri Lynn Schellenberg, Homira Osman, Maria Masnata, et al.
Clinical Chemistry|April 28, 2023
Analytical and Non-Analytical Variation May Lead to Inappropriate Antimicrobial Dosing in Neonates: An In Silico StudyThi A Nguyen, Ranita Kirubakaran, Hayley B Schultz, et al.
Neurology|June 17, 2016
Disease burden and functional outcomes in congenital myotonic dystrophy: A cross-sectional studyNicholas E Johnson, Russell Butterfield, Kiera Berggren, et al.
Developmental Medicine and Child Neurology|October 30, 2015
Parent-reported multi-national study of the impact of congenital and childhood onset myotonic dystrophyNicholas E Johnson, Anne-Berit Ekstrom, Craig Campbell, et al.
Science (New York, N.Y.)|November 11, 2009
Pathogenesis of chytridiomycosis, a cause of catastrophic amphibian declinesJamie Voyles, Sam Young, Lee Berger, et al.
Journal of Comparative Effectiveness Research|October 25, 2021
Meta-analyses of deflazacort versus prednisone/prednisolone in patients with nonsense mutation Duchenne muscular dystrophyPerry B Shieh, Gary Elfring, Panayiota Trifillis, et al.
Muscle & Nerve|July 28, 2016
Myostatin inhibitor ACE-031 treatment of ambulatory boys with Duchenne muscular dystrophy: Results of a randomized, placebo-controlled clinical trialCraig Campbell, Hugh J McMillan, Jean K Mah, et al.
Pageof 19