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Plos One|December 20, 2012
Characterisation and validation of insertions and deletions in 173 patient exomesFrancesco Lescai, Silvia Bonfiglio, Chiara Bacchelli, et al.
The Lancet. Child & Adolescent Health|May 15, 2020
The effect of lactoferrin supplementation on death or major morbidity in very low birthweight infants (LIFT): a multicentre, double-blind, randomised controlled trialWilliam O Tarnow-Mordi, Mohamed E Abdel-Latif, Andrew Martin, et al.
BMC Infectious Diseases|April 7, 2026
Optimising COVID-19 episode identification using serology and PCR/rapid antigen testing: insights from the BRACE trialEllie McDonald, Laure F Pittet, Marc Bonten, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|May 26, 2007
Genetics of epilepsy: epilepsy research foundation workshop reportSanjay Sisodiya, J Helen Cross, Ingmar Blümcke, et al.
Nature Biotechnology|July 17, 2018
Multiplexed identification, quantification and genotyping of infectious agents using a semiconductor biochipArjang Hassibi, Arun Manickam, Rituraj Singh, et al.
Neurobiology of Aging|September 3, 2020
Analysis of DNM3 and VAMP4 as genetic modifiers of LRRK2 Parkinson's diseaseEmmeline E Brown, Cornelis Blauwendraat, Joanne Trinh, et al.
Vaccine|July 27, 2025
Longitudinal Meta-cohort study protocol using systems biology to identify vaccine safety biomarkersJoann Diray-Arce, Ana C Chang, Sara Moradipoor, et al.
Vaccine|May 17, 2026
SARS-CoV-2 Ancestral and Omicron variant immunity in Australian children in 2023, a seroprevalence studyArchana Koirala, Shayal A Prasad, M Christian Tjiam, et al.
Cell Reports|July 27, 2012
Mutations in the gene PRRT2 cause paroxysmal kinesigenic dyskinesia with infantile convulsionsHsien-Yang Lee, Yong Huang, Nadine Bruneau, et al.
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