Left atrial dysfunction in sickle cell anemia is associated with diffuse myocardial fibrosis, increased right ventricular pressure and reduced exercise capacity.
Alsaied, T; Niss, O; Tretter, JT; Powell, AW; Chin, C; Fleck, RJ; Cnota, JF; Malik, P; Quinn, CT; Nagueh, SM; et al.
Scientific Reports.
2020;
10.
Severe infusion-related reaction to crizanlizumab in an adolescent with sickle cell disease.
Karkoska, K; Quinn, CT; Clapp, K; McGann, PT.
American Journal of Hematology.
2020;
95:E338-E339.
Hydroxyurea Optimization through Precision Study (HOPS): study protocol for a randomized, multicenter trial in children with sickle cell anemia.
Meier, ER; Creary, SE; Heeney, MM; Dong, M; Appiah-Kubi, AO; Nelson, SC; Niss, O; Piccone, C; Quarmyne, M; Quinn, CT; et al.
Trials.
2020;
21.
Improving self-management in adolescents with sickle cell disease.
Crosby, LE; Hood, A; Kidwell, K; Nwankwo, C; Peugh, J; Strong, H; Quinn, C; Britto, MT.
Pediatric Blood and Cancer.
2020;
67.
Non-transfusion-dependent ß-thalassemia because of a single ß-thalassemia mutation and coinherited a-globin gene triplication: Need for increased awareness to prevent incorrect and delayed diagnosis.
Gurunathan, A; Tarango, C; McGann, PT; Niss, O; Quinn, CT.
Journal of Pediatric Hematology/Oncology.
2020;
42:e494-e496.
Non–transfusion-dependent β-Thalassemia Because of a Single β-Thalassemia Mutation and Coinherited α-Globin Gene Triplication: Need for Increased Awareness to Prevent Incorrect and Delayed Diagnosis.
Gurunathan, A; Tarango, C; McGann, PT; Niss, O; Quinn, CT.
Journal of Pediatric Hematology/Oncology.
2020;
42:e494-e496.
Disease Self-Efficacy and Health-Related Quality of Life in Adolescents with Sickle Cell Disease.
Goldstein-Leever, A; Peugh, JL; Quinn, CT; Crosby, LE.
Journal of Pediatric Hematology/Oncology.
2020;
42:141-144.
Clinical utility of confirmatory genetic testing to differentiate sickle cell trait from sickle-β+thalassemia by newborn screening.
Shook, LM; Haygood, D; Quinn, CT.
International Journal of Neonatal Screening.
2020;
6:7-7.
Vitamin D supplementation and pain-related emergency department visits in children with sickle cell disease.
Hood, AM; Quinn, CT; King, CD; Shook, LM; Peugh, JL; Crosby, LE.
Complementary Therapies in Medicine.
2020;
49:102342-102342.
L-glutamine for sickle cell disease: Knight or pawn?.
Sadaf, A; Quinn, CT.
Experimental biology and medicine (Maywood, N.J.).
2020;
245:146-154.