1. Matos, M. A., Leandro, M. P., Sa, C. K. C., & Serra, F. D. P. (2020). Complicações osteoarticulares na anemia falciforme. In C. Salles, C. Dias, & A. M. Ladeia (Eds.), Anemia Falciforme e comorbidades associadas na infância e na adolescência (pp. 67–87). Curitiba.
2. Worrall, D., Smith-Whitley, K., & Wells, L. (2016). Hemoglobin to hematocrit ratio: the strongest predictor of femoral head osteonecrosis in children with sickle cell disease. Journal of Pediatric Orthopedics, 36(2), 139–144.
3. Mukisi-Mukaza, M., Saint Martin, C., Etienne-Julan, M., Donkerwolcke, M., Burny, M. E., & Burny, F. (2011). Risk factors and impact of orthopaedic monitoring on the outcome of avascular necrosis of the femoral head in adults with sickle cell disease: 215 patients case study with control group. Orthopaedics and Traumatology: Surgery and Research, 97(8), 814–820.
4. Matos, M. A., Silva, L. L. S., Alves, G. B., Alcântara Júnior, W. S., & Veiga, D. (2018). Necrosis of the femoral head and health-related quality of life of children and adolescents. Acta Ortopedica Brasileira, 26(4), 227–230.
5. Malheiros, C. D., Lisle, L., Castelar, M., Sá, K. N., & Matos, M. A. (2015). Hip dysfunction and quality of life in patients with sickle cell disease. Clinical Pediatric (Phila), 54(14), 1354–1358.