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Sleep & Breathing = Schlaf & Atmung|January 13, 2017
Hydroxyurea treatment effect on children with sickle cell disease and obstructive sleep apneaAnthony J Grady, Jane S Hankins, Brent Haberman, et al.
Pediatric Nephrology (Berlin, Germany)|May 12, 2011
Glomerular hyperfiltration and albuminuria in children with sickle cell anemiaBanu Aygun, Nicole A Mortier, Matthew P Smeltzer, et al.
Pediatric Blood & Cancer|May 7, 2009
Simultaneous acute splenic sequestration and transient aplastic crisis in children with sickle cell diseaseAmber Mayfield Yates, Jane S Hankins, Nicole A Mortier, et al.
Journal of Pediatric Hematology/Oncology|November 6, 2019
The Adolescent and Caregiver Sickle Cell Disease Self-management Skills Checklist: Preliminary Reliability and ValidityMegan Loew, Justin L Williams, Kathryn Russell, et al.
Journal of Magnetic Resonance Imaging : JMRI|February 26, 2021
Quantitative Susceptibility Mapping Using a Multispectral Autoregressive Moving Average Model to Assess Hepatic Iron OverloadAaryani Tipirneni-Sajja, Ralf B Loeffler, Jane S Hankins, et al.
British Journal of Haematology|February 4, 2022
Neurocognitive risk in sickle cell disease: Utilizing neuropsychology services to manage cognitive symptoms and functional limitationsJennifer N Longoria, Andrew M Heitzer, Jane S Hankins, et al.
Experimental Biology and Medicine (Maywood, N.J.)|March 5, 2016
Original Research: Parvovirus B19 infection in children with sickle cell disease in the hydroxyurea eraJane S Hankins, Rhiannon R Penkert, Paul Lavoie, et al.
American Journal of Hematology|March 9, 2023
Longitudinal effect of disease-modifying therapy on left ventricular diastolic function in children with sickle cell anemiaParul Rai, Victoria I Okhomina, Guolian Kang, et al.
Frontiers in Pediatrics|April 9, 2024
Awareness, access, and communication: provider perspectives on early intervention services for children with sickle cell diseaseAndrew M Heitzer, Erin MacArthur, Mollie Tamboli, et al.
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