Hereditary angioedema in Spain: medical care and patient journey.

Autor:	Caballero, Teresa1,2,3 (AUTHOR) mteresa.caballero@ciberer.es, Alonso, Carmen4 (AUTHOR), Luisa Baeza, María5,6 (AUTHOR), Baynova, Krasimira7 (AUTHOR), Cabeza, José8 (AUTHOR), Cortés, Isabel9 (AUTHOR), Escobar Oblitas, Danilo10,11 (AUTHOR), Guilarte, Mar12 (AUTHOR), Joral, Alejandro13 (AUTHOR), Jurado Palomo, Jesús14 (AUTHOR), Lara Jiménez, María Ángeles15 (AUTHOR), Martínez Virto, Ana16 (AUTHOR), Medrano, Laura17 (AUTHOR), Monte Boquet, Emilio18 (AUTHOR), Navarro, Montserrat19 (AUTHOR), Pérez, Diego20 (AUTHOR), Plá Martí, María José21 (AUTHOR), Smith Foltz, Sara L.17 (AUTHOR), Suero, Coral22 (AUTHOR), Zamora, Carolina17 (AUTHOR)
Zdroj:	Orphanet Journal of Rare Diseases. 5/21/2024, Vol. 19 Issue 1, p1-10. 10p. 4 Diagrams, 1 Chart.
Databáze:	Academic Search Ultimate
Externí odkaz:	Zobrazit plný text záznamu