Source: Journal of Pain and Symptom Management. Unidade: EERP
Subjects: ANEMIA FALCIFORME, DOR, ENFRENTAMENTO, DOENÇAS HEMATOLÓGICAS
ABNT
HYACINTH, Octavia et al. Pain experience, physical function, pain coping, and catastrophizing in children with sickle cell disease who had normal and abnormal sensory patterns. Journal of Pain and Symptom Management, v. 60, n. 6, p. 1079-1091, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.jpainsymman.2020.07.006. Acesso em: 05 nov. 2024.APA
Hyacinth, O., Silva-Rodrigues, F. M., Nunes, M. D. R., Lopes Júnior, L. C., Fernandes, A., Nascimento, L. C., & Jacob, E. (2020). Pain experience, physical function, pain coping, and catastrophizing in children with sickle cell disease who had normal and abnormal sensory patterns. Journal of Pain and Symptom Management, 60( 6), 1079-1091. doi:10.1016/j.jpainsymman.2020.07.006NLM
Hyacinth O, Silva-Rodrigues FM, Nunes MDR, Lopes Júnior LC, Fernandes A, Nascimento LC, Jacob E. Pain experience, physical function, pain coping, and catastrophizing in children with sickle cell disease who had normal and abnormal sensory patterns [Internet]. Journal of Pain and Symptom Management. 2020 ; 60( 6): 1079-1091.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1016/j.jpainsymman.2020.07.006Vancouver
Hyacinth O, Silva-Rodrigues FM, Nunes MDR, Lopes Júnior LC, Fernandes A, Nascimento LC, Jacob E. Pain experience, physical function, pain coping, and catastrophizing in children with sickle cell disease who had normal and abnormal sensory patterns [Internet]. Journal of Pain and Symptom Management. 2020 ; 60( 6): 1079-1091.[citado 2024 nov. 05 ] Available from: https://doi.org/10.1016/j.jpainsymman.2020.07.006