Brazilian Guidelines for Hereditary Angioedema Management - 2017 Update Part 1: Definition, Classification and Diagnosis

Hereditary angioedema is an autosomal dominant disease characterized by recurrent angioedema attacks with the involvement of multiple organs. The disease is unknown to many health professionals and is therefore underdiagnosed. Patients who are not adequately diagnosed and treated have an estimated m...

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Αποθηκεύτηκε σε:
Λεπτομέρειες βιβλιογραφικής εγγραφής
Κύριοι συγγραφείς: Pedro Giavina-Bianchi, Luisa Karla Arruda, Marcelo V. Aun, Regis A. Campos, Herberto J. Chong-Neto, Rosemeire N. Constantino-Silva, Fátima R. Fernandes, Maria F. Ferraro, Mariana P.L. Ferriani, Alfeu T. França, Gustavo Fusaro, Juliana F.B. Garcia, Shirley Komninakis, Luana S.M. Maia, Eli Mansour, Adriana S. Moreno, Antonio A. Motta, João B. Pesquero, Nathalia Portilho, Nelson A. Rosário, Faradiba S. Serpa, Dirceu Solé, Priscila Takejima, Eliana Toledo, Solange O.R. Valle, Camila L. Veronez, Anete S. Grumach
Μορφή: Artigo
Γλώσσα:Inglês
Έκδοση: Faculdade de Medicina / USP 2018-05-01
Σειρά:Clinics
Θέματα:
Hereditary Angioedema
Angioedema
C1 Inhibitor Deficiency
Coagulation Factor XII Mutations
Management, Guidelines
Διαθέσιμο Online:http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1807-59322018000100303&lng=en&tlng=en
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