Clinical features of a Brazilian family with hereditary angioedema with normal C1 inhibitor and mutation in F12 gene (2016)
- Autores:
- Autor USP: ARRUDA, LUISA KARLA DE PAULA - FMRP
- Unidade: FMRP
- Assuntos: ANGIOEDEMA; HEREDITARIEDADE; DOENÇAS RARAS; MUTAÇÃO GENÉTICA
- Idioma: Inglês
- Imprenta:
- Local: Copenhagen
- Data de publicação: 2016
- Fonte:
- Nome do evento: Congress of European Academy of Allergy and Clinical Immunology (EAACI)
-
ABNT
FERRIANI, M. P. L. et al. Clinical features of a Brazilian family with hereditary angioedema with normal C1 inhibitor and mutation in F12 gene. Allergy. Copenhagen: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 19 set. 2024. , 2016 -
APA
Ferriani, M. P. L., Maia, L., Nociti, T. M., Dias, M. M., Moreno, A. S., & Arruda, L. K. de P. (2016). Clinical features of a Brazilian family with hereditary angioedema with normal C1 inhibitor and mutation in F12 gene. Allergy. Copenhagen: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. -
NLM
Ferriani MPL, Maia L, Nociti TM, Dias MM, Moreno AS, Arruda LK de P. Clinical features of a Brazilian family with hereditary angioedema with normal C1 inhibitor and mutation in F12 gene. Allergy. 2016 ; 71 555.[citado 2024 set. 19 ] -
Vancouver
Ferriani MPL, Maia L, Nociti TM, Dias MM, Moreno AS, Arruda LK de P. Clinical features of a Brazilian family with hereditary angioedema with normal C1 inhibitor and mutation in F12 gene. Allergy. 2016 ; 71 555.[citado 2024 set. 19 ] - Co-sensitization to cockroach and mite is not simply explained by tropomyosin cross-reactivity
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