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Handbook of Cystic Fibrosis
This 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 lat...
| Clasificación: | Libro Electrónico |
|---|---|
| Autores principales: | , , |
| Autor Corporativo: | |
| Formato: | Electrónico eBook |
| Idioma: | Inglés |
| Publicado: |
Cham :
Springer International Publishing : Imprint: Adis,
2016.
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| Edición: | 1st ed. 2016. |
| Temas: | |
| Acceso en línea: | Texto Completo |
MARC
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| 005 | 20220114142404.0 | ||
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| 020 | |a 9783319325040 |9 978-3-319-32504-0 | ||
| 024 | 7 | |a 10.1007/978-3-319-32504-0 |2 doi | |
| 050 | 4 | |a RC705-779 | |
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| 100 | 1 | |a Filbrun, Amy G. |e author. |4 aut |4 http://id.loc.gov/vocabulary/relators/aut | |
| 245 | 1 | 0 | |a Handbook of Cystic Fibrosis |h [electronic resource] / |c by Amy G. Filbrun, Thomas Lahiri, Clement L Ren. |
| 250 | |a 1st ed. 2016. | ||
| 264 | 1 | |a Cham : |b Springer International Publishing : |b Imprint: Adis, |c 2016. | |
| 300 | |a XII, 99 p. 9 illus., 7 illus. in color. |b online resource. | ||
| 336 | |a text |b txt |2 rdacontent | ||
| 337 | |a computer |b c |2 rdamedia | ||
| 338 | |a online resource |b cr |2 rdacarrier | ||
| 347 | |a text file |b PDF |2 rda | ||
| 505 | 0 | |a Introduction 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 | |a This 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. | ||
| 650 | 0 | |a Respiratory organs-Diseases. | |
| 650 | 1 | 4 | |a Pneumology. |
| 700 | 1 | |a Lahiri, Thomas. |e author. |4 aut |4 http://id.loc.gov/vocabulary/relators/aut | |
| 700 | 1 | |a Ren, Clement L. |e author. |4 aut |4 http://id.loc.gov/vocabulary/relators/aut | |
| 710 | 2 | |a SpringerLink (Online service) | |
| 773 | 0 | |t Springer Nature eBook | |
| 776 | 0 | 8 | |i Printed edition: |z 9783319325026 |
| 776 | 0 | 8 | |i Printed edition: |z 9783319325033 |
| 856 | 4 | 0 | |u https://doi.uam.elogim.com/10.1007/978-3-319-32504-0 |z Texto Completo |
| 912 | |a ZDB-2-SME | ||
| 912 | |a ZDB-2-SXM | ||
| 950 | |a Medicine (SpringerNature-11650) | ||
| 950 | |a Medicine (R0) (SpringerNature-43714) | ||