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Titlebook: Handbook of Cystic Fibrosis; Amy G. Filbrun,Thomas Lahiri,Clement L Ren Book 2016 Springer International Publishing Switzerland 2016 CFTR

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樓主: EVOKE
21#
發(fā)表于 2025-3-25 06:08:02 | 只看該作者
The Rise of Effective Treatments, of CF care has become even brighter with the development of CFTR modulators; medications that can target the underlying defect causing CF. Currently available CFTR modulators target only a small proportion of patients with CF or lack potency, although, newer more effective compounds are under devel
22#
發(fā)表于 2025-3-25 11:23:44 | 只看該作者
23#
發(fā)表于 2025-3-25 14:45:05 | 只看該作者
,Uniqueness of meromorphic functions on ?,tic fibrosis transmembrane conductance regulator (CFTR) modulator therapies heralds a new era in CF care, their full impact on CF remains to be determined, and older patients with CF are likely to still have complications of CF that need to be addressed.
24#
發(fā)表于 2025-3-25 17:42:00 | 只看該作者
25#
發(fā)表于 2025-3-25 22:20:02 | 只看該作者
26#
發(fā)表于 2025-3-26 02:14:12 | 只看該作者
Bernhard Kramann,Manfred SchmelingCystic fibrosis (CF) is a multisystem disease, and its clinical features reflect the broad impact that loss of cystic fibrosis transmembrane conductance regulator (CFTR) function has on multiple organs (Fig. .). However, pulmonary and gastrointestinal disease account for the vast majority of morbidity and mortality in CF.
27#
發(fā)表于 2025-3-26 07:35:15 | 只看該作者
Clinical Features and Complications of Cystic Fibrosis,Cystic fibrosis (CF) is a multisystem disease, and its clinical features reflect the broad impact that loss of cystic fibrosis transmembrane conductance regulator (CFTR) function has on multiple organs (Fig. .). However, pulmonary and gastrointestinal disease account for the vast majority of morbidity and mortality in CF.
28#
發(fā)表于 2025-3-26 12:23:36 | 只看該作者
Amy G. Filbrun,Thomas Lahiri,Clement L RenConcise yet complete overview of the epidemiology, pathophysiology, and clinical features of cystic fibrosis and an in-depth review of the most up-to-date methods of diagnosis, symptom management, and
29#
發(fā)表于 2025-3-26 12:56:43 | 只看該作者
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30#
發(fā)表于 2025-3-26 20:41:00 | 只看該作者
https://doi.org/10.1007/978-3-319-32504-0CFTR mutations; Cystic Fibrosis; Cystic Fibrosis manifestations; Pulmonary; Respiratory medicine
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