Assessing alternative treatment targets in patients with cystic fibrosis
Author:
Affiliation:
1. 1. Division of Pulmonary, Critical Care, and Sleep Disorders. Department of Medicine. University of Louisville, Louisville, KY
2. 2. Programa de Pós Graduação em Ciências Médicas Universidade Federal de Santa Catarina (UFSC), Florianópolis,SC
Publisher
Sociedade Brasileira de Pneumologia e Tisiologia
Reference16 articles.
1. 1. Ministério da Saúde. Protocolo clínico e diretrizes terapêuticas da fibrose cística. 2022. Protocolos clínicos e diretrizes terapêuticas.
2. 2. Ong T, Ramsey BW. Cystic Fibrosis: A Review. Jama. Jun 6 2023;329(21):1859-1871. doi:10.1001/jama.2023.8120
3. 3. Cystic Fibrosis Foundation. 2022 Annual Data Report. 2023. Cystic Fibrosis Foundation Patient Registry. https://www.cff.org/medical- professionals/patient-registry
4. 4. Varkki SD, Aaron R, Chapla A, et al. CFTR mutations and phenotypic correlations in people with cystic fibrosis: a retrospective study from a single centre in south India. The Lancet Regional Health-Southeast Asia. 2024;27
5. 5. Grupo Brasileiro de Estudos de Fibrose Cística. Relatório anual de 2021. 2021. Registro brasileiro de fibrose cística ano 2021. http:// www.gbefc.org.br/ingles/site/pagina.php?idpai=128&id=15
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