Showing results (341-350 of 365) with videos related to

Sort By:
Pageof 37
American Journal of Human Genetics|January 17, 2012
PRRT2 mutations cause benign familial infantile epilepsy and infantile convulsions with choreoathetosis syndromeSarah E Heron, Bronwyn E Grinton, Sara Kivity, et al.
Critical Care and Resuscitation : Journal of the Australasian Academy of Critical Care Medicine|October 25, 2023
Protocol and statistical analysis plan for the mega randomised registry trial comparing conservative vs. liberal oxygenation targets in adults with nonhypoxic ischaemic acute brain injuries and conditions in the intensive care unit (Mega-ROX Brains)Paul J Young, Abdulrahman Al-Fares, Diptesh Aryal, et al.
Chest|January 23, 2025
Long-Term Mental Health Morbidity in Adult Survivors of COVID-19 Critical Illness: A Population-Based Cohort StudyShannon M Fernando, Danial Qureshi, Robert Talarico, et al.
Resuscitation|April 10, 2016
Targeted therapeutic mild hypercapnia after cardiac arrest: A phase II multi-centre randomised controlled trial (the CCC trial)Glenn M Eastwood, Antoine G Schneider, Satoshi Suzuki, et al.
Journal of Human Nutrition and Dietetics : the Official Journal of the British Dietetic Association|November 26, 2024
Nutrition delivery during hospitalisation after critical illness in Australia and New Zealand: a multicentre, prospective observational studyEmma J Ridley, Kate Ainscough, Michael Bailey, et al.
Critical Care and Resuscitation : Journal of the Australasian Academy of Critical Care Medicine|October 25, 2023
Protocol summary and statistical analysis plan for the low oxygen intervention for cardiac arrest injury limitation (LOGICAL) trialPaul J Young, Carol L Hodgson, Diane Mackle, et al.
Critical Care and Resuscitation : Journal of the Australasian Academy of Critical Care Medicine|October 25, 2023
Protocol and statistical analysis plan for the mega randomised registry trial comparing conservative vs. liberal oxygenation targets in adults with sepsis in the intensive care unit (Mega-ROX Sepsis)Paul J Young, Abdulrahman Al-Fares, Diptesh Aryal, et al.
Neurology|March 14, 2014
GABRA1 and STXBP1: novel genetic causes of Dravet syndromeGemma L Carvill, Sarah Weckhuysen, Jacinta M McMahon, et al.
American Journal of Human Genetics|March 1, 2008
Array-based gene discovery with three unrelated subjects shows SCARB2/LIMP-2 deficiency causes myoclonus epilepsy and glomerulosclerosisSamuel F Berkovic, Leanne M Dibbens, Alicia Oshlack, et al.
Pageof 37