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Revista De Neurologia|April 3, 2009
[Attention deficit hyperactivity behavioral phenotype dimensions of adults from Antioquian families using the Wender-Utah Scale -Spanish version]N Trujillo-Orrego, D A Pineda, C P Arango, et al.Acta Ortopedica Mexicana|November 27, 2020
[Alteration of X-ray measurements in proximal humerus osteosynthesis with intramedullary nail]E A Valencia-Ramón, E Hazan-Lasri, E Pineda-Gómez, et al.Revista De Neurologia|March 4, 2010
[Utility of the Wender-Utah rating scale and the checklists for the diagnosis of familial attention deficit hyperactivity disorder in adults. Convergent and concurrent validities]David A Pineda, Natalia Trujillo-Orrego, Daniel C Aguirre-Acevedo, et al.Journal of the National Cancer Institute|September 27, 2023
Cascade testing for hereditary cancer: comprehensive multigene panels identify unexpected actionable findings in relativesBrandie Heald, Sara Pirzadeh-Miller, Rachel E Ellsworth, et al.Nature|October 8, 2020
Four annular structures in a protostellar disk less than 500,000 years oldDominique M Segura-Cox, Anika Schmiedeke, Jaime E Pineda, et al.Biorxiv : the Preprint Server for Biology|January 8, 2024
Neoantigen Cancer Vaccines and Different Immune Checkpoint Therapies Each Utilize Both Converging and Distinct Mechanisms that in Combination Enable Synergistic Therapeutic EfficacySunita Keshari, Alexander S Shavkunov, Qi Miao, et al.Medicine and Science in Sports and Exercise|April 18, 2024
Validation of Polar Elixir™ Pulse Oximeter against Arterial Blood Gases during Stepwise Steady-State Inspired HypoxiaMonica K Russell, John F Horton, Christian A Clermont, et al.Physical Review Letters|February 16, 2024
Connection between Mechanical Relaxation and Equilibration Kinetics in a High-Entropy Metallic GlassY J Duan, M Nabahat, Yu Tong, et al.Biorxiv : the Preprint Server for Biology|February 9, 2026
Antigen presentation requirements for effective cDC1-based cancer immunotherapyJosué E Pineda, Tomoyuki Minowa, Li Shen, et al.Human Genetics|February 17, 2010
Heterozygous mutations in SIX3 and SHH are associated with schizencephaly and further expand the clinical spectrum of holoprosencephalyUte Hehr, Daniel E Pineda-Alvarez, Goekhan Uyanik, et al.Pageof 16