TY  - JOUR
AU  - Caballero, Teresa
AU  - Alonso, Carmen
AU  - Baeza, María Luisa
AU  - Baynova, Krasimira
AU  - Cabeza, José
AU  - Cortés, Isabel
AU  - Escobar Oblitas, Danilo
AU  - Guilarte, Mar
AU  - Joral, Alejandro
AU  - Jurado Palomo, Jesús
AU  - Lara Jiménez, María Ángeles
AU  - Martínez Virto, Ana
AU  - Medrano, Laura
AU  - Monte Boquet, Emilio
AU  - Navarro, Montserrat
AU  - Pérez, Diego
AU  - Plá Martí, María José
AU  - Smith Foltz, Sara L
AU  - Suero, Coral
AU  - Zamora, Carolina
PY  - 2024
DO  - 10.1186/s13023-024-03182-1
UR  - https://hdl.handle.net/20.500.13003/20498
T2  - Orphanet journal of rare diseases
AB  - 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 characteristics of the...
LA  - eng
M2  - 210
PB  - BMC
KW  - Quality of Life
KW  - Male
KW  - Spain
KW  - Female
KW  - Humans
KW  - Angioedemas, Hereditary
TI  - Hereditary angioedema in Spain: medical care and patient journey
TY  - research article
VL  - 19
ER  -