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Frontiers in Pediatrics|March 13, 2023
Retinopathy of prematurity and placental histopathology findings: A retrospective cohort studySam Ebenezer Athikarisamy, Geoffrey C Lam, Matthew N Cooper, et al.ACS Biomaterials Science & Engineering|June 16, 2022
Promoter Identification and Optimization for the Response of Lactobacillus plantarum WCFS1 to the Gram-Negative Pathogen-Associated Molecule N-3-Oxododecanoyl Homoserine LactoneJoseph R Spangler, Denver N Cooper, Anthony P Malanoski, et al.Frontiers in Psychiatry|February 14, 2022
Examining Effectiveness and Predictors of Treatment Response of Pivotal Response Treatment in Autism: An Umbrella Review and a Meta-AnalysisMirko Uljarević, Wesley Billingham, Matthew N Cooper, et al.Journal of Neurology, Neurosurgery, and Psychiatry|January 11, 2002
Evaluation of the management of optic neuritis: audit on the neurological and ophthalmological practice in the north west of EnglandA Ghosh, S P Kelly, J Mathews, et al.BMC Public Health|December 8, 2020
Racial discrimination and allostatic load among First Nations Australians: a nationally representative cross-sectional studyLeah Cave, Matthew N Cooper, Stephen R Zubrick, et al.American Journal of Surgery|April 1, 1977
Preoperative intra-aortic balloon assist in high risk revascularization patientsG N Cooper, A K Singh, L L Vargas, et al.International Journal for Equity in Health|September 8, 2019
Caregiver-perceived racial discrimination is associated with diverse mental health outcomes in Aboriginal and Torres Strait Islander children aged 7-12 yearsLeah Cave, Matthew N Cooper, Stephen R Zubrick, et al.European Journal of Neurology|February 3, 2011
Acute meningo-encephalitis in pregnancy-a problem of differential diagnosisP N Cooper, D Neary, D Denning, et al.Aging|July 22, 2011
New comparative genomics approach reveals a conserved health span signature across speciesMichael Antosh, David Fox, Stephen L Helfand, et al.Human Genomics|June 30, 2011
A meta-analysis of single base-pair substitutions in translational termination codons ('nonstop' mutations) that cause human inherited diseaseStephen E Hamby, Nick S T Thomas, David N Cooper, et al.Pageof 124