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_aRC858.C95 _b2016 EB |
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_aFilbrun, Amy G. _999244 _0Local |
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_aHandbook of Cystic Fibrosis _cby Amy G Filbrun, Thomas Lahiri, Clement L Ren |
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_aCham _bSpringer International Publishing _bImprint _bAdis _c2016 |
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_a1 recurso en línea (XII, 99 páginas) _b9 ilustraciones, 7 ilustraciones en color |
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| 505 | 0 | _aIntroduction and epidemiology of cystic fibrosis -- Pathophysiology of cystic fibrosis -- Clinical features and complications of cystic fibrosis -- Diagnosis of cystic fibrosis -- Monitoring and evaluation of patients with cystic fibrosis -- Treatment of cystic fibrosis. | |
| 520 | 3 | _aThis concise manual provides clinicians and other related health care professionals with an essential reference tool to the background of cystic fibrosis, and the management and treatment of this disease. The latest guidelines are reviewed and current and emerging treatments are discussed in the latter chapters. Cystic fibrosis is an inherited condition where a mutation in the gene coding for the cystic fibrosis transmembrane conductance regulator (CFTR) causes loss of function. The dysfunction of CFTR results in the production of thick mucus in the lungs and digestive tract, causing pulmonary and gastrointestinal manifestations. The incidence of cystic fibrosis in Europe and the US ranges between 1 in 2,000 and 1 in 25,000. | |
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_aLahiri, Thomas _0Local _999245 |
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_aRen, Clement L. _999246 _0Local |
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_uhttps://go.openathens.net/redirector/universidadeuropea.es?url=https://link.springer.com/book/10.1007/978-3-319-32504-0 _zAcceso a este recurso digital (usuarios Universidad Europea de Madrid) |
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