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Hemoglobin Chapel Hill masquerading as hemoglobin S in newborn sickle cell screening: A case study

Volodko N, Parker ML, Ridsdale R, MacNeil L, Sosova I, Estey MP, Proctor D, Olayinka L, Newbigging A, Bordeleau P, Powell M, Higgins V

The relation between sleep and pain sensitization in pediatric sickle cell disease

Kell PA, Morris MC, Wilde ZC, Golden AP, Dickens H, Williams-Kirkwood W, Ford HA, Karlson CW

Addressing Primary Care Needs in People Living With Sickle Cell Disease: A Narrative Review

Patel A, Wright C, Klein RJ, Nguemeni Tiako MJ, Kuo AA, Cronin RM

Patterns of hormonal contraception use in women with sickle cell disease and employer-sponsored insurance

O’Brien SH, Della-Moretta SL, Stanek JR, Creary SE, Roe AH, Xu W, Bala N, Vesely SK, Hardy RY

Sickle Cell Pain: Call for Whole Person Health Approaches to Mechanisms-informed Integrative Management

Adams-Mitchell C, Ajiboye R, Stephen JK, AlHassan K, Keagle MJ, Ezenwa MO, Duckworth L PhD, ARNP, Yoon SJ, Schlaeger J, Jenerette C, Campbell CM, Molokie R, Wang ZJ, Wilkie DJ.