Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Ana Martínez Virto"'
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
Publikováno v:
Atención Primaria, Vol 47, Iss 6, Pp 386-388 (2015)
Externí odkaz:
https://doaj.org/article/e617dcdff2d548efa3d765476887ad7c
Publikováno v:
Atencion Primaria
Repisalud
Instituto de Salud Carlos III (ISCIII)
Repisalud
Instituto de Salud Carlos III (ISCIII)
Sí
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::633a15aafc0925d17bb8559db57ebaa3
http://europepmc.org/articles/PMC6837090
http://europepmc.org/articles/PMC6837090
Autor:
Antonio, Sarría Santamera, Javier, Prado Galbarro, Manuel, Quintana Díaz, Ana, Martínez Virto
Publikováno v:
Atencion Primaria
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::fb4401d541aa78f1a61752dce38d5ceb
https://pubmed.ncbi.nlm.nih.gov/25573446
https://pubmed.ncbi.nlm.nih.gov/25573446