Brazilian guidelines for the pharmacological treatment of the pulmonary symptoms of cystic fibrosis. Official document of the Sociedade Brasileira de Pneumologia e Tisiologia (SBPT, Brazilian Thoracic Association)

Cystic fibrosis (CF) is a genetic disease that results in dysfunction of the CF transmembrane conductance regulator (CFTR) protein, which is a chloride and bicarbonate channel expressed in the apical portion of epithelial cells of various organs. Dysfunction of that protein results in diverse clinic...

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Detalles Bibliográficos
Autores principales: Athanazio, Rodrigo Abensur, Tanni, Suzana Erico, Ferreira, Juliana, Dalcin, Paulo de Tarso Roth, de Fuccio, Marcelo B, Esposito, Concetta, Canan, Mariane Gonçalves Martynychen, Coelho, Liana Sousa, Firmida, Mônica de Cássia, de Almeida, Marina Buarque, Marostica, Paulo José Cauduro, Monte, Luciana de Freitas Velloso, Souza, Edna Lúcia, Pinto, Leonardo Araujo, Rached, Samia Zahi, de Oliveira, Verônica Stasiak Bednarczuk, Riedi, Carlos Antonio, da Silva, Luiz Vicente Ribeiro Ferreira
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Pneumologia e Tisiologia 2023
Materias:
Special Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10171269/
https://www.ncbi.nlm.nih.gov/pubmed/37194817
http://dx.doi.org/10.36416/1806-3756/e20230040

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10171269/
https://www.ncbi.nlm.nih.gov/pubmed/37194817
http://dx.doi.org/10.36416/1806-3756/e20230040

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