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Movement Disorders : Official Journal of the Movement Disorder Society|March 18, 2026
The Movement Disorder Spectrum of ATP1A3-Related Disorders: Cross-Sectional Analysis and Video Archive of 88 PatientsKaterina Bernardi, Anna Zhou, Kathryn Yang, et al.
Critical Care Explorations|November 13, 2023
Pharmacologic and Genetic Downregulation of Proprotein Convertase Subtilisin/Kexin Type 9 and Survival From SepsisPatrick R Lawler, Garen Manvelian, Alida Coppi, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|February 26, 2022
Efficacy and Safety of Sarilumab in Hospitalized Patients With Coronavirus Disease 2019: A Randomized Clinical TrialSumathi Sivapalasingam, David J Lederer, Rafia Bhore, et al.
Medrxiv : the Preprint Server for Health Sciences|November 24, 2025
Divergent T Cell Phenotypes Define Pediatric Crohn's Disease and Ulcerative ColitisLeonard Nettey, Hengqi Betty Zheng, Joseph C Devlin, et al.
Nature Genetics|August 5, 2024
Genetic risk factors for COVID-19 and influenza are largely distinctJack A Kosmicki, Anthony Marcketta, Deepika Sharma, et al.
Nature|March 7, 2022
Whole-genome sequencing reveals host factors underlying critical COVID-19Athanasios Kousathanas, Erola Pairo-Castineira, Konrad Rawlik, et al.
American Journal of Human Genetics|June 11, 2021
Pan-ancestry exome-wide association analyses of COVID-19 outcomes in 586,157 individualsJack A Kosmicki, Julie E Horowitz, Nilanjana Banerjee, et al.
Medrxiv : the Preprint Server for Health Sciences|March 3, 2021
A catalog of associations between rare coding variants and COVID-19 outcomesJ A Kosmicki, J E Horowitz, N Banerjee, et al.
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