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Nature Medicine|June 5, 2019
Identification of rare-disease genes using blood transcriptome sequencing and large control cohortsLaure Frésard, Craig Smail, Nicole M Ferraro, et al.Science (New York, N.Y.)|September 11, 2020
Transcriptomic signatures across human tissues identify functional rare genetic variationNicole M Ferraro, Benjamin J Strober, Jonah Einson, et al.Frontiers in Immunology|February 11, 2025
Plasma IL-17A is increased in patients with critical MIS-C and associated to in-hospital mortalityEmmerson C F de Farias, Luciana M P P do Nascimento, Manoel J C Pavão Junior, et al.Scientific Reports|March 6, 2024
Factors associated to mortality in children with critical COVID-19 and multisystem inflammatory syndrome in a resource-poor settingEmmerson C F de Farias, Manoel J C Pavão Junior, Susan C D de Sales, et al.JAMA Neurology|August 30, 2021
Association of Variants in the SPTLC1 Gene With Juvenile Amyotrophic Lateral SclerosisJanel O Johnson, Ruth Chia, Danny E Miller, et al.Pageof 34