Psychometric study of the SF-36v2 in hereditary angioedema due to C1 inhibitor deficiency (C1-INH-HAE).

MLA

Palao-Ocharan, Paola, et al. “Psychometric Study of the SF-36v2 in Hereditary Angioedema Due to C1 Inhibitor Deficiency (C1-INH-HAE).” Orphanet Journal of Rare Diseases, vol. 17, no. 1, Mar. 2022, pp. 1–14. EBSCOhost, https://doi.org/10.1186/s13023-022-02202-2.

APA

Palao-Ocharan, P., Prior, N., Pérez-Fernández, E., Caminoa, M., DV-HAE-QoL Study Group, Aberer, W., Betschel, S., Bygum, A., Campos, R. A., Csuka, D., Farkas, H., Gómez-Traseira, C., Grumach, A. S., Leibovich, I., Malbran, A., Moldovan, D., Mihaly, E., Obtulowicz, K., Porebski, G., & Reshef, A. (2022). Psychometric study of the SF-36v2 in hereditary angioedema due to C1 inhibitor deficiency (C1-INH-HAE). Orphanet Journal of Rare Diseases, 17(1), 1–14. https://doi.org/10.1186/s13023-022-02202-2

Chicago

Palao-Ocharan, Paola, Nieves Prior, Elia Pérez-Fernández, Magdalena Caminoa, DV-HAE-QoL Study Group, W. Aberer, S. Betschel, et al. 2022. “Psychometric Study of the SF-36v2 in Hereditary Angioedema Due to C1 Inhibitor Deficiency (C1-INH-HAE).” Orphanet Journal of Rare Diseases 17 (1): 1–14. doi:10.1186/s13023-022-02202-2.