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JAMIA Open|June 15, 2026
Early prediction of unplanned critical care transfers in children using EHR-based ensemble machine learningEamonn Tweedy, Sanjiv Mehta, Mark V Mai, et al.Pediatrics|October 7, 2024
Using ChatGPT to Provide Patient-Specific Answers to Parental Questions in the PICUR Brandon Hunter, Satid Thammasitboon, Sreya S Rahman, et al.BMC Neurology|December 14, 2018
Batten disease: biochemical and molecular characterization revealing novel PPT1 and TPP1 gene mutations in Indian patientsJayesh Sheth, Mehul Mistri, Riddhi Bhavsar, et al.Journal of Child Neurology|December 3, 2025
Delayed Bilateral Internal Carotid Artery Occlusion in a Pediatric Patient Following Traumatic Injury: Insights on Management and Interventional ApproachSamuel J Belfer, Lauren A Beslow, Alexander Vaz, et al.BMC Neurology|August 5, 2023
Comparative yield of molecular diagnostic algorithms for autism spectrum disorder diagnosis in India: evidence supporting whole exome sequencing as first tier testFrenny Sheth, Jhanvi Shah, Deepika Jain, et al.Pediatric Research|October 4, 2025
Comparison of vasopressin to epinephrine during pediatric in-hospital cardiac arrest: survival and physiologic responsivenessMorgann Loaec, Garrett Keim, Kathryn Graham, et al.Epilepsia Open|August 16, 2023
Landscape of genetic infantile epileptic spasms syndrome-A multicenter cohort of 124 children from IndiaBalamurugan Nagarajan, Vykuntaraju K Gowda, Sangeetha Yoganathan, et al.Orphanet Journal of Rare Diseases|August 13, 2024
Burden of rare genetic disorders in India: twenty-two years' experience of a tertiary centreJayesh Sheth, Aadhira Nair, Frenny Sheth, et al.Pageof 2