| Autor: |
Veronez, Camila Lopes, Mendes, Agatha Ribeiro, Leite, Caroliny Souza, Gomes, Caio Perez, Grumach, Anete Sevciovic, Pesquero, João Bosco, Cagini, Nathália, Mansour, Eli, da Silva, Jane, Giavina-Bianchi, Pedro, Teixeira, Ana Júlia, Valle, Solange Rodrigues, Goudouris, Ekaterini, Serpa, Faradiba Sarquis, Moyses, Therezinha R., Campinhos, Fernanda Lugão, Ensina, Luis Felipe, Aranda, Carolina Sánchez, Rizzo, Maria Cândida, Campos, Régis A., Gonçalves, Rozana Fátima, Minafra, Fernanda Gontijo, de Souza Bernardes, Marli, Chong-Neto, Herberto José, Filho, Nelson Rosário, Guth, Carolina, Toledo, Eliana, Coelho Dias, Gabriela Andrade, Piccirillo, Miguel Alberto, Severo Ferreira, Janáira Fernandes, Marcelino, Fernanda Casares, da Rocha Rolins Neto, Pedro, Franco, Jackeline Motta, Pafume de Sá, Gustavo, Garro, Laila Sabino, Carolina da Matta Ain, Ana, Velasco, Helena F., Fernandes Carvalho, Ellaine Dóris, Fernandes Carvalho de Andrade, Maria Denise, Boll, Cristiane Alves, Ferraroni, Natasha Rebouças, Martins Pinto Swensson, Ana Carolina, Vilela Rabelo, Leandro Augusto, Pacheco de Figueiredo, Joanemile, Figueredo, Raphael Coelho, Mendes, Ronney Corrêa, Sales, Valéria S.F., Bacarini Leite, Luiz Fernando, Beltran Moschione Castro, Ana Paula, Ferreira Mascarenhas, Elke C., Teixeira, Thais Bomfim, Campos Teixeira, Camila A., Pereira de Lira Marques, Adriana, Pires Amaral Resende, Ludmilla Luzia, Sandrin, Leda das Neves Almeida, Tavares, Clarissa Soares |
| Zdroj: |
The Journal of Allergy and Clinical Immunology: In Practice; June 2021, Vol. 9 Issue: 6 p2293-2304.e5 |
| Abstrakt: |
Primary angioedema (PA) is a complex disorder, presenting multiple hereditary (hereditary angioedema) and acquired subtypes (acquired angioedema). Despite a very similar clinical presentation among subtypes, the differential diagnosis is limited by the difficulty to identify bradykinin-mediated PA and the lack of specific biomarkers. |
| Databáze: |
Supplemental Index |
| Externí odkaz: |
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