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Journal of Personalized Medicine|October 27, 2023
Associations of Muscle Strength with Central Aspects of Pain: Data from the Knee Pain and Related Health in the Community (KPIC) CohortDaniel F McWilliams, Bin Yue, Stephanie L Smith, et al.
IEEE Transactions on Visualization and Computer Graphics|August 16, 2017
Cognitive Cost of Using Augmented Reality DisplaysJames Baumeister, Seung Youb Ssin, Neven A M ElSayed, et al.
American Journal of Medical Genetics. Part A|October 15, 2015
Novel loss-of-function variants in DIAPH1 associated with syndromic microcephaly, blindness, and early onset seizuresAlmundher Al-Maawali, Brenda J Barry, Anna Rajab, et al.
Antioxidants (Basel, Switzerland)|February 27, 2026
Three-Month Administration of PB125 Modifies Histopathology, Redox Homeostasis, and Mobility in the Hartley Guinea Pig Model of Primary OsteoarthritisKendra M Andrie, Robert V Musci, Maureen A Walsh, et al.
Human Molecular Genetics|November 18, 1998
LIS1 and XLIS (DCX) mutations cause most classical lissencephaly, but different patterns of malformationD T Pilz, N Matsumoto, S Minnerath, et al.
European Respiratory Review : an Official Journal of the European Respiratory Society|May 28, 2025
Determining the minimum important differences for field walking tests in adults with long-term conditions: a systematic review and meta-analysisEnya Daynes, Ruth E Barker, Amy V Jones, et al.
Cancer Discovery|August 14, 2021
Rates and Patterns of Clonal Oncogenic Mutations in the Normal Human BrainJavier Ganz, Eduardo A Maury, Basheer Becerra, et al.
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