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pro vyhledávání: '"Sara L. Smith Foltz"'
Autor:
Teresa Caballero, Carmen Alonso, María Luisa Baeza, Krasimira Baynova, José Cabeza, Isabel Cortés, Danilo Escobar Oblitas, Mar Guilarte, Alejandro Joral, Jesús Jurado Palomo, María Ángeles Lara Jiménez, Ana Martínez Virto, Laura Medrano, Emilio Monte Boquet, Montserrat Navarro, Diego Pérez, María José Plá Martí, Sara L. Smith Foltz, Coral Suero, Carolina Zamora
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-10 (2024)
Abstract Background Hereditary angioedema due to C1 inhibitor deficiency (HAE-C1INH) is a genetic rare disease characterized by recurrent, transient and unpredictable episodes of cold, non-pruriginous oedema without associated urticaria. The characte
Externí odkaz:
https://doaj.org/article/a96a217dd8ac4bbaba933f0299cf8e67
