ReP USP - Resultado da busca

Filtros : "School of Medicine of Santa Casa de Misericórdia of Vitória, Vitória, ES" "Moreno, Adriana Santos" Limpar

Filtros

USP affiliated authors
- arruda, luisa karla de paula (2)
- dias, marina mendonça (2)
- silva junior, wilson araújo da (2)
- aragon, davi casale (1)
- dias, fabrício césar (1)

Collaboration
Normalized affiliation
- universidade estadual paulista júlio de mesquita filho (unesp) (~1)
- universidade de são paulo (usp) (~1)
Non normalized affiliation
- federal university of rio de janeiro, clementino fraga filho university hospital, rio de janeiro, rj (2)
- school of medicine of santa casa de misericórdia of vitória, vitória, es (2)
- johannes-gutenberg university, mainz (1)
- johannes-gutenberg university, mainz, germany (1)
- joseph-fourier university of grenoble, grenoble, france (1)

Artigo de periodico-carta/editorial
Genotype‐phenotype correlations in Brazilian patients with hereditary angioedema due to C1 inhibitor deficiency. [Carta] (2019)
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
Source: Allergy. Unidades: FMRP, FM, ICB
Subjects: BRADICININA, ANGIOEDEMA, DOENÇAS HEREDITÁRIAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 01 jun. 2024. , 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 2024 jun. 01 ] 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 2024 jun. 01 ] Available from: https://doi.org/10.1111/all.13699
Artigo de periodico
Coagulation factor XII gene mutation in Brazilian families with hereditary angioedema with normal C1 inhibitor (2015)
Moreno, Adriana Santos; Valle, Solange Oliveira Rodrigues; Levy, Soloni ; França, Alfeu Tavares; Serpa, Faradiba S. ; Arcuri, Helen Andrade; Palma, Mario Sérgio; Campos, Wagner Narciso de; Dias, Marina M. ; Ponard, Denise ; Monnier, Nicole; Lunardi, Joel ; Bork, Konrad ; Silva Júnior, Wilson Araújo da; Arruda, Luisa Karla de Paula
Source: International Archives of Allergy and Immunology. Unidade: FMRP
Subjects: ANGIOEDEMA, DNA, REAÇÃO EM CADEIA POR POLIMERASE, DOENÇAS HEREDITÁRIAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MORENO, Adriana Santos et al. Coagulation factor XII gene mutation in Brazilian families with hereditary angioedema with normal C1 inhibitor. International Archives of Allergy and Immunology, v. 166, n. 2, p. 114-120, 2015Tradução . . Disponível em: https://doi.org/10.1159/000376547. Acesso em: 01 jun. 2024.
APA
Moreno, A. S., Valle, S. O. R., Levy, S. , França, A. T., Serpa, F. S. , Arcuri, H. A., et al. (2015). Coagulation factor XII gene mutation in Brazilian families with hereditary angioedema with normal C1 inhibitor. International Archives of Allergy and Immunology, 166( 2), 114-120. doi:10.1159/000376547
NLM
Moreno AS, Valle SOR, Levy S , França AT, Serpa F S , Arcuri HA, Palma MS, Campos WN de, Dias M M , Ponard D , Monnier N, Lunardi J , Bork K , Silva Júnior WA da, Arruda LK de P. Coagulation factor XII gene mutation in Brazilian families with hereditary angioedema with normal C1 inhibitor [Internet]. International Archives of Allergy and Immunology. 2015 ; 166( 2): 114-120.[citado 2024 jun. 01 ] Available from: https://doi.org/10.1159/000376547
Vancouver
Moreno AS, Valle SOR, Levy S , França AT, Serpa F S , Arcuri HA, Palma MS, Campos WN de, Dias M M , Ponard D , Monnier N, Lunardi J , Bork K , Silva Júnior WA da, Arruda LK de P. Coagulation factor XII gene mutation in Brazilian families with hereditary angioedema with normal C1 inhibitor [Internet]. International Archives of Allergy and Immunology. 2015 ; 166( 2): 114-120.[citado 2024 jun. 01 ] Available from: https://doi.org/10.1159/000376547

Digital Library of Intellectual Production of Universidade de São Paulo 2012 - 2024