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Indian Journal of Critical Care Medicine : Peer-Reviewed, Official Publication of Indian Society of Critical Care Medicine|March 10, 2023
Competencies for Point-of-care Ultrasonography in ICU: An ISCCM Expert Panel Practice RecommendationShrikanth Srinivasan, Praveen G Kumar, Deepak Govil, et al.Spine|May 3, 2023
Perioperative Complications and Health-related Quality of Life Outcomes in Severe Pediatric Spinal DeformityMunish C Gupta, Lawrence G Lenke, Sachin Gupta, et al.Journal of Neurosurgery. Spine|August 5, 2023
Predictive role of global spinopelvic alignment and upper instrumented vertebra level in symptomatic proximal junctional kyphosis in adult spinal deformityJichao Ye, Sachin Gupta, Ali S Farooqi, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 10, 2023
Poison exon annotations improve the yield of clinically relevant variants in genomic diagnostic testingStephanie A Felker, James M J Lawlor, Susan M Hiatt, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 1, 2020
Clinical outcomes of a genomic screening program for actionable genetic conditionsAdam H Buchanan, H Lester Kirchner, Marci L B Schwartz, et al.Journal of Neurosurgery. Spine|June 16, 2023
Use of multiple rods and proximal junctional kyphosis in adult spinal deformity surgeryJichao Ye, Sachin Gupta, Ali S Farooqi, et al.Stroke|June 25, 2025
Thrombectomy Versus Medical Management for Pediatric Arterial Ischemic Stroke With Large Baseline InfarctKartik D Bhatia, Prakash Muthusami, Carmen Parra-Farinas, et al.Ebiomedicine|April 29, 2023
CSF neopterin, quinolinic acid and kynurenine/tryptophan ratio are biomarkers of active neuroinflammationJingya Yan, Kavitha Kothur, Shekeeb Mohammad, et al.Brain : a Journal of Neurology|February 9, 2022
Activating RAC1 variants in the switch II region cause a developmental syndrome and alter neuronal morphologySiddharth Banka, Abigail Bennington, Martin J Baker, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 5, 2018
Adaptation and validation of the ACMG/AMP variant classification framework for MYH7-associated inherited cardiomyopathies: recommendations by ClinGen's Inherited Cardiomyopathy Expert PanelMelissa A Kelly, Colleen Caleshu, Ana Morales, et al.Pageof 42