Avaliação da colonização pulmonar e do estado nutricional em crianças e adolescentes com fibrose cística, antes e após a triagem neonatal
=== 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 protein transmembrane conductance regulator. Newborn screening is importa...
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| Format: | Others |
| Language: | Portuguese |
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Universidade Federal de Minas Gerais
2012
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| Online Access: | http://hdl.handle.net/1843/BUOS-93CNWL |