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Cerebellum (London, England)|December 16, 2024
Case Series of Cerebellar Ataxia with Tremor Due to Heterozygous STUB1 Variants (SCA48) without TBP Expansions: Further Evidence for SCA48 as a Monogenic DiseaseYan Zochowski, Kishore R Kumar, Matthew Katz, et al.Tissue Engineering. Part C, Methods|February 21, 2014
Cellular reporter systems for high-throughput screening of interactions between bioactive matrices and human mesenchymal stromal cellsRegina Duryagina, Konstantinos Anastassiadis, Manfred F Maitz, et al.The New England Journal of Medicine|October 6, 2006
Ranibizumab versus verteporfin for neovascular age-related macular degenerationDavid M Brown, Peter K Kaiser, Mark Michels, et al.American Journal of Ophthalmology|October 24, 2007
Ranibizumab for predominantly classic neovascular age-related macular degeneration: subgroup analysis of first-year ANCHOR resultsPeter K Kaiser, David M Brown, Kang Zhang, et al.Disability and Rehabilitation|March 13, 2026
A mixed methods study exploring factors that impact physiotherapy participation for people with Parkinson's diseaseBeth Cunningham, Lindsay Hepnar, Robyn Lamont, et al.Chemistry & Biology|December 23, 2006
Metabolic engineering of Pseudomonas putida for methylmalonyl-CoA biosynthesis to enable complex heterologous secondary metabolite formationFrank Gross, Michael W Ring, Olena Perlova, et al.The Journal of Urology|August 20, 2013
Microsurgical rat varicocele modelBobby B Najari, Philip S Li, Ranjith Ramasamy, et al.Current Oncology (Toronto, Ont.)|September 27, 2023
Real-Time Ultrasound-Computed Tomography Fusion with Volume Navigation to Assess Pancreatic Cystic LesionsManoj Mathew, Mayur Virarkar, Jia Sun, et al.Retina (Philadelphia, Pa.)|March 6, 2020
PHASE 2 STUDY OF THE SAFETY AND EFFICACY OF BRIMONIDINE DRUG DELIVERY SYSTEM (BRIMO DDS) GENERATION 1 IN PATIENTS WITH GEOGRAPHIC ATROPHY SECONDARY TO AGE-RELATED MACULAR DEGENERATIONBaruch D Kuppermann, Sunil S Patel, David S Boyer, et al.Frontiers in Neurology|February 13, 2023
Case report: Adult-onset limb girdle muscular dystrophy in sibling pair due to novel homozygous LAMA2 missense variantMatthew Katz, Leigh B Waddell, Michaela Yuen, et al.Pageof 10