Improving care of hereditary angioedema with C1 inhibitor deficiency (type 1 and type 2 hereditary angioedema) in Latin America
J. investig. allergol. clin. immunol
; 24(6): 445-447, sept.-oct. 2014. tab
Article
in English
| IBECS
| ID: ibc-130597
Responsible library:
ES1.1
Localization: BNCS
Full text:
Available
Collection:
National databases
/
Spain
Database:
IBECS
Main subject:
Sterol Esterase
/
Complement C1 Inhibitor Protein
/
Angioedemas, Hereditary
/
Hereditary Angioedema Types I and II
Type of study:
Diagnostic study
Limits:
Female
/
Humans
/
Male
Language:
English
Journal:
J. investig. allergol. clin. immunol
Year:
2014
Document type:
Article
Institution/Affiliation country:
1Instituto Argentino de Alergia e Inmunología/Argentina
/
Clínica San Pablo/Perú
/
Clínica de San Salvador/El Salvador
/
Faculty of Medicine ABC/Brazil
/
Hospital Luis Calvo Mackenna/Chile
/
Hospital México/Costa Rica
/
Hospital Pediátrico Prof. J P Garrahan/Argentina
/
Hospital San Fernando/Panama
/
Hospital de Niños Ricardo Gutierrez/Argentina
/
Instituto Nacional de Pediatría/México