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Annals of Hematology|December 6, 2024
Livedoid vasculopathy in hemoglobinopathy-associated chronic leg ulcersHarish Eswaran, Samuel Wilson, Jane Little, et al.
Kidney360|May 31, 2023
Emerging Therapies and Advances in Sickle Cell Disease with a Focus on Renal ManifestationsMofiyin Obadina, Sam Wilson, Vimal K Derebail, et al.
Clinical Medicine (London, England)|April 23, 2010
The trainee-led clinicopathological conference: an innovative method for educating medical traineesElspeth Potton, Jane Little, Jim Campbell, et al.
Blood Advances|February 8, 2022
GRNDaD: big data and sickle cell diseaseSophie Lanzkron, Deepa Manwani, Payal Desai, et al.
Pediatric Blood & Cancer|January 27, 2022
Building the foundation of health-related knowledge via near-peer education for children with sickle cell diseaseElaissa L Trybus Hardy, Brenda Williams, Christopher Harden, et al.
Microcirculation (New York, N.Y. : 1994)|January 21, 2017
Normal saline is associated with increased sickle red cell stiffness and prolonged transit times in a microfluidic model of the capillary systemMarcus A Carden, Meredith Fay, Yumiko Sakurai, et al.
Pediatric Blood & Cancer|August 27, 2025
Virtual Transition Assessments in Sickle Cell Disease Are Feasible and Available Transition Instruments May Highlight Different Components of the Transition ExperienceAlexandra Boye-Doe, Samuel Wilson, Lindsey Akpuogu, et al.
Transfusion|March 9, 2019
Challenges in the treatment and prevention of delayed hemolytic transfusion reactions with hyperhemolysis in sickle cell disease patientsChristina L Dean, Cheryl L Maier, Satheesh Chonat, et al.
Pediatric Blood & Cancer|July 20, 2019
Splenectomy is not associated with a higher tricuspid regurgitant jet velocity in people with sickle cell anemiaArpan A Sinha, Tanvi Adusumilli, Hillel W Cohen, et al.
Healthcare Quarterly (Toronto, Ont.)|June 25, 2008
Safe medication swallowing in Dysphagia: a collaborative improvement projectLawrence D Jackson, Jane Little, Edward Kung, et al.
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