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Journal of Palliative Medicine|October 13, 2023
Palliative Care in Survivors of Critical Illness: A Qualitative Study of Post-Intensive Care Unit Program CliniciansTammy L Eaton, Taylor E Lincoln, Anna Lewis, et al.
ATS Scholar|April 19, 2021
COVID-19 and the Early-Career Physician-Scientist. Fostering Resilience beyond the PandemicCorrine R Kliment, Ian J Barbash, Jacob S Brenner, et al.
Blood|July 8, 2026
The CYB5R3 T117S Missense Variant is Associated with Attenuated Riociguat Efficacy in Sickle Cell DiseaseKatherine C Wood, Seyed Mehdi Nouraie, Mark T Gladwin, et al.
Experimental Biology and Medicine (Maywood, N.J.)|August 19, 2021
Progression of central nervous system disease from pediatric to young adulthood in sickle cell anemiaGrace Champlin, Scott N Hwang, Andrew Heitzer, et al.
British Journal of Haematology|April 6, 2007
Genetic polymorphisms associated with priapism in sickle cell diseaseLaine Elliott, Allison E Ashley-Koch, Laura De Castro, et al.
JAMA Internal Medicine|April 2, 2019
Clinician-Family Communication About Patients' Values and Preferences in Intensive Care UnitsLeslie P Scheunemann, Natalie C Ernecoff, Praewpannarai Buddadhumaruk, et al.
The Lancet. Haematology|March 15, 2025
Crizanlizumab with or without hydroxyurea in patients with sickle cell disease (STAND): primary analyses from a placebo-controlled, randomised, double-blind, phase 3 trialMiguel R Abboud, Rodolfo D Cançado, Mariane De Montalembert, et al.
Scientific Reports|November 16, 2019
Machine Learning to Quantitate Neutrophil NETosisLaila Elsherif, Noah Sciaky, Carrington A Metts, et al.
British Journal of Haematology|July 9, 2024
Persistent albuminuria and chronic kidney disease in adults with sickle cell anaemia: Results from a multicenter natural history studyLaura Y Zhou, Vimal K Derebail, Payal C Desai, et al.
British Journal of Haematology|August 19, 2011
Tapered oral dexamethasone for the acute chest syndrome of sickle cell diseaseCharles T Quinn, Marie J Stuart, Karen Kesler, et al.
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