Genotype‐phenotype correlations in Brazilian patients with hereditary angioedema due to C1 inhibitor deficiency. [Carta] (2019)
- Authors:
- Maia, Luana Sella Motta
- Moreno, Adriana Santos
- Ferriani, Mariana Paes Leme
- Nunes, Fernanda Leonel
- Ferraro, Maria Fernanda
- Dias, Marina Mendonça
- Roxo-Junior, Pérsio
- Dias, Fabrício Moura
- Valle, Solange Oliveira Rodrigues
- Levy, Soloni
- Alonso, Maria Luiza Oliva
- França, Alfeu Tavares
- Serpa, Faradiba Sarquis
- Motta, Antônio Abílio
- Maia, Felipe Gonçalves Motta
- Aragon, Davi Casale
- Sarti, Willy
- Silva Junior, Wilson Araújo da
- Bork, Konrad
- Cichon, Sven
- Arruda, Luisa Karla de Paula
- Maia, Luana Sella Motta
- USP affiliated authors: DIAS, MARINA MENDONÇA - FMRP ; ROXO JÚNIOR, PÉRSIO - FMRP ; ARAGON, DAVI CASALE - FMRP ; SARTI, WILLY - FMRP ; SILVA JUNIOR, WILSON ARAÚJO DA - FMRP ; ARRUDA, LUISA KARLA DE PAULA - FMRP ; MAIA, LUANA SELLA MOTTA - FMRP ; MORENO, ADRIANA SANTOS - FMRP ; FERRIANI, MARIANA PAES LEME - FM ; NUNES, FERNANDA LEONEL - FMRP ; DIAS, FABRÍCIO CÉSAR - FMRP ; MAIA, FELIPE GONÇALVES MOTTA - ICB
- Unidades: FMRP; FM; ICB
- DOI: 10.1111/all.13699
- Subjects: BRADICININA; ANGIOEDEMA; DOENÇAS HEREDITÁRIAS
- Agências de fomento:
- Language: Inglês
- Imprenta:
- Publisher place: West Sussex
- Date published: 2019
- Source:
- Este periódico é de assinatura
- Este artigo NÃO é de acesso aberto
- Cor do Acesso Aberto: closed
-
ABNT
MAIA, Luana Sella Motta et al. Genotype‐phenotype correlations in Brazilian patients with hereditary angioedema due to C1 inhibitor deficiency. [Carta]. Allergy. West Sussex: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. Disponível em: https://doi.org/10.1111/all.13699. Acesso em: 27 dez. 2025. , 2019 -
APA
Maia, L. S. M., Moreno, A. S., Ferriani, M. P. L., Nunes, F. L., Ferraro, M. F., Dias, M. M., et al. (2019). Genotype‐phenotype correlations in Brazilian patients with hereditary angioedema due to C1 inhibitor deficiency. [Carta]. Allergy. West Sussex: Faculdade de Medicina de Ribeirão Preto, Universidade de São Paulo. doi:10.1111/all.13699 -
NLM
Maia LSM, Moreno AS, Ferriani MPL, Nunes FL, Ferraro MF, Dias MM, Roxo-Junior P, Dias FM, Valle SOR, Levy S , Alonso MLO, França AT, Serpa FS, Motta AA, Maia FGM, Aragon DC, Sarti W, Silva Junior WA da, Bork K , Cichon S, Arruda LK de P. Genotype‐phenotype correlations in Brazilian patients with hereditary angioedema due to C1 inhibitor deficiency. [Carta] [Internet]. Allergy. 2019 ; 74( 5): 1013-1016.[citado 2025 dez. 27 ] Available from: https://doi.org/10.1111/all.13699 -
Vancouver
Maia LSM, Moreno AS, Ferriani MPL, Nunes FL, Ferraro MF, Dias MM, Roxo-Junior P, Dias FM, Valle SOR, Levy S , Alonso MLO, França AT, Serpa FS, Motta AA, Maia FGM, Aragon DC, Sarti W, Silva Junior WA da, Bork K , Cichon S, Arruda LK de P. Genotype‐phenotype correlations in Brazilian patients with hereditary angioedema due to C1 inhibitor deficiency. [Carta] [Internet]. Allergy. 2019 ; 74( 5): 1013-1016.[citado 2025 dez. 27 ] Available from: https://doi.org/10.1111/all.13699 - A cost-effective algorithm for diagnosis of hereditary angioedema with normal C1 inhibitor.: applying molecular approach to clinical practice
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- A multidisciplinary intervention resulted in improvement in qualilty of life among patients with hereditary angioedema
- Gene mapping strategy for Alu elements rearrangements: detection of new large deletions in the SERPING1 gene causing hereditary angioedema in Brazilian families
- Study of angiopoietin and plasminogen genes in hereditary angioedema
- Mutações no gene serping1 em pacientes brasileiros com angioedema hereditário
- Coagulation factor XII gene mutation in Brazilian families with hereditary angioedema with normal C1 inhibitor
Informações sobre o DOI: 10.1111/all.13699 (Fonte: oaDOI API)
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