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Neurology|December 22, 2017
Silent cerebral infarct definitions and full-scale IQ loss in children with sickle cell anemiaNatasha A Choudhury, Michael R DeBaun, Mark Rodeghier, et al.
Southern Medical Journal|September 7, 2016
Effect of Free Dental Services on Individuals with Sickle Cell DiseaseLauren N Whiteman, Carlton Haywood, Sophie Lanzkron, et al.
Pediatric Critical Care Medicine : a Journal of the Society of Critical Care Medicine and the World Federation of Pediatric Intensive and Critical Care Societies|November 9, 2010
Glial fibrillary acidic protein as a brain injury biomarker in children undergoing extracorporeal membrane oxygenationMelania M Bembea, William Savage, John J Strouse, et al.
Journal of Clinical & Experimental Nephrology|July 15, 2016
Typical Hus: Evidence of Acute Phase Complement Activation from a Daycare OutbreakTammy M Brady, Cozumel Pruette, Lauren F Loeffler, et al.
Southern Medical Journal|September 7, 2016
Symptomatic Avascular Necrosis: An Understudied Risk Factor for Acute Care Utilization by Patients with SCDTiffany Yu, Timothy Campbell, Isabella Ciuffetelli, et al.
Case Reports in Hematology|August 20, 2013
Patent foramen ovale in patients with sickle cell disease and stroke: case presentations and review of the literatureSheila Razdan, John J Strouse, Rakhi Naik, et al.
International Journal of Environmental Research and Public Health|November 16, 2016
Secondhand Smoke Is an Important Modifiable Risk Factor in Sickle Cell Disease: A Review of the Current Literature and Areas for Future ResearchS Christy Sadreameli, Benjamin T Kopp, Susan E Creary, et al.
The Journal of Pediatrics|December 3, 2014
Transcranial Doppler screening of Medicaid-insured children with sickle cell diseaseDavid G Bundy, Michael T Abrams, John J Strouse, et al.
Clinical Trials (London, England)|February 18, 2014
Attitudes toward clinical trials among patients with sickle cell diseaseCarlton Haywood, Sophie Lanzkron, Marie Diener-West, et al.
Blood Cells, Molecules & Diseases|November 20, 2013
New insights provided by a comparison of impaired deformability with erythrocyte oxidative stress for sickle cell diseaseViachaslau M Barodka, Enika Nagababu, Joy G Mohanty, et al.
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