Showing results (61-70 of 140) with videos related to
Sort By:
Pageof 14
American Journal of Human Genetics|December 9, 2022
Genome-wide analysis of copy-number variation in humans with cleft lip and/or cleft palate identifies COBLL1, RIC1, and ARHGEF38 as clefting genesLisa A Lansdon, Amanda Dickinson, Sydney Arlis, et al.Trials|June 17, 2011
Paramedic Initiated Lisinopril For Acute Stroke Treatment (PIL-FAST): study protocol for a pilot randomised controlled trialLisa Shaw, Christopher Price, Sally McLure, et al.Plos One|May 30, 2013
Global gene expression profiling of individual human oocytes and embryos demonstrates heterogeneity in early developmentLisa Shaw, Sharon F Sneddon, Leo Zeef, et al.Trials|December 16, 2025
Development of a core outcome set for the assessment of spasticity in adults: a study protocolBridget Hill, Stephan Ashford, Hannah Barden, et al.British Paramedic Journal|June 11, 2026
A survey of UK emergency medical services' approach to incidental identification of atrial fibrillationLaura Blair, Graham McClelland, Lisa Shaw, et al.Human Heredity|June 13, 2009
Genome scan, fine-mapping, and candidate gene analysis of non-syndromic cleft lip with or without cleft palate reveals phenotype-specific differences in linkage and association resultsMary L Marazita, Andrew C Lidral, Jeffrey C Murray, et al.Emergency Medicine Journal : EMJ|October 1, 2013
Paramedic Initiated Lisinopril For Acute Stroke Treatment (PIL-FAST): results from the pilot randomised controlled trialLisa Shaw, Christopher Price, Sally McLure, et al.International Journal of Stroke : Official Journal of the International Stroke Society|March 16, 2021
Cost-effectiveness of an enhanced Paramedic Acute Stroke Treatment Assessment (PASTA) during emergency stroke care: Economic results from a pragmatic cluster randomized trialNawaraj Bhattarai, Christopher I Price, Peter McMeekin, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 14, 2009
Prevalence and nonrandom distribution of exonic mutations in interferon regulatory factor 6 in 307 families with Van der Woude syndrome and 37 families with popliteal pterygium syndromeRenata L L Ferreira de Lima, Sarah A Hoper, Michella Ghassibe, et al.BMJ Open|December 25, 2025
Development of a Standardised stroke risk assessment for patients with MigraAinous symptoms Reviewed as suspected TIA (SMART): study protocol for a mixed methods studyLisa Shaw, Jemma Isaac, Jason Scott, et al.Pageof 14