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Undersea & Hyperbaric Medicine : Journal of the Undersea and Hyperbaric Medical Society, Inc|August 2, 2017
Applying quality improvement methods in a hyperbaric oxygen program: reducing unnecessary glucose testingSarah L Stevens, Atsushi Sorita, Anthony J Narr, et al.
Arthritis & Rheumatology (Hoboken, N.J.)|December 5, 2015
Development of Th17-Associated Interstitial Kidney Inflammation in Lupus-Prone Mice Lacking the Gene Encoding STAT-1Gloria Yiu, Tue K Rasmussen, Bahareh Ajami, et al.
Journal of the American Chemical Society|July 18, 2001
Perchlorophenalenyl radicalP A Koutentis, Y Chen, Y Cao, et al.
Frontiers in Behavioral Neuroscience|October 31, 2025
Different frequencies of human scalp-recorded theta activity may index integration of activity in distinct recurrent cortico-subcortical mnemonic networksInanna K Haddon, Rohan O C King, Dylan A Taylor, et al.
The Journal of Thoracic and Cardiovascular Surgery|March 1, 1990
Heparin dosing and monitoring for cardiopulmonary bypass. A comparison of techniques with measurement of subclinical plasma coagulationG P Gravlee, W S Haddon, H K Rothberger, et al.
Surgery|September 17, 2025
Patient-reported health-related social needs obtained at the bedside and outcomes after elective major surgeryKurt S Schultz, Miranda S Moore, Emily Y Park, et al.
JCI Insight|January 24, 2020
Integrated, multicohort analysis reveals unified signature of systemic lupus erythematosusWinston A Haynes, D James Haddon, Vivian K Diep, et al.
Arthritis Research & Therapy|June 14, 2015
Gene expression changes reflect clinical response in a placebo-controlled randomized trial of abatacept in patients with diffuse cutaneous systemic sclerosisEliza F Chakravarty, Viktor Martyanov, David Fiorentino, et al.
Plos One|July 19, 2012
Multilevel-3D bit patterned magnetic media with 8 signal levels per nanocolumnNissim Amos, John Butler, Beomseop Lee, et al.
Research Involvement and Engagement|July 14, 2026
Public involvement and co-design of longitudinal studies of sleep health alongside young people with rare genetic conditionsJulie P Clayton, Josephine E Haddon, Jessica Hall, et al.
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