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Shwachman-Kulczycki score still useful to monitor cystic fibrosis severity
(Faculdade de Medicina / USP, 2011)
INTRODUCTION: The Shwachman-Kulczycki score was the first scoring system used in cystic fibrosis to assess disease severity. Despite its subjectivity, it is still widely used. OBJECTIVE: To study correlations among forced ...
Nasal and paranasal sinus endoscopy, computed tomography and microbiology of upper airways and the correlations with genotype and severity of cystic fibrosis
(Elsevier Ireland LtdClareIrlanda, 2007)
Bhalla, Kanga And Shwachman-kulczycki Score On Cystic Fibrosis: A Look By The Modifier Genes
(WILEY-BLACKWELLHOBOKEN, 2016)
Desempenho da ressonância magnética para avaliação das alterações pulmonares em crianças com fibrose cística
(Pontifícia Universidade Católica do Rio Grande do SulPorto Alegre, 2015)
Introduction : Cystic fibrosis is a chronic disease that requires regular monitoring and testing. Chest CT is the gold standard to the evaluation of the pulmonary parenchyma, but because of the risk caused by radiation, ...
Desempenho da ressonância magnética para avaliação das alterações pulmonares em crianças com fibrose cística
(Pontifícia Universidade Católica do Rio Grande do SulPorto Alegre, 2015)
Introduction : Cystic fibrosis is a chronic disease that requires regular monitoring and testing. Chest CT is the gold standard to the evaluation of the pulmonary parenchyma, but because of the risk caused by radiation, ...
Fibrose cística em um centro de referência no Brasil: características clínicas e laboratoriais de 104 pacientes e sua associação com o genótipo e a gravidade da doençaCystic fibrosis at a Brazilian center of excellence: clinical and laboratory characteristics of 104 patients and their association with genotype and disease severity
(Sociedade Brasileira de Pediatria, 2004)
Avaliação da colonização pulmonar e do estado nutricional em crianças e adolescentes com fibrose cística, antes e após a triagem neonatal
(Universidade Federal de Minas GeraisUFMG, 2012-05-16)
Introduction: Cystic Fibrosis (CF) is a genetic disease of the exocrine glands, autosomal recessive, which involves multiple organs and cause great diversity of clinical problems arising from the change in function of the ...
Avaliação da qualidade de vida de pacientes com fibrose cística por meio do Cystic Fibrosis QuestionnaireQuality of life assessment in patients with cystic fibrosis by means of the Cystic Fibrosis Questionnaire
(Sociedade Brasileira de Pneumologia e Tisiologia, 2011)