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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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發(fā)表于 2025-3-21 18:42:27 | 只看該作者 |倒序瀏覽 |閱讀模式
書目名稱Handbook of Cystic Fibrosis
編輯Amy G. Filbrun,Thomas Lahiri,Clement L Ren
視頻videohttp://file.papertrans.cn/422/421123/421123.mp4
概述Concise 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
圖書封面Titlebook: Handbook of Cystic Fibrosis;  Amy G. Filbrun,Thomas Lahiri,Clement L Ren Book 2016 Springer International Publishing Switzerland 2016 CFTR
描述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.
出版日期Book 2016
關鍵詞CFTR mutations; Cystic Fibrosis; Cystic Fibrosis manifestations; Pulmonary; Respiratory medicine
版次1
doihttps://doi.org/10.1007/978-3-319-32504-0
isbn_softcover978-3-319-32502-6
isbn_ebook978-3-319-32504-0
copyrightSpringer International Publishing Switzerland 2016
The information of publication is updating

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https://doi.org/10.1007/978-3-030-54363-1ng cassette proteins. It is expressed in multiple tissues throughout the body, where it plays a key role in the regulation of ion transport across cell membranes in mucosal surfaces [1]. CFTR conducts chloride (Cl) and bicarbonate (HCO.), and it also appears to reduce sodium (Na) transport through i
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Pathophysiology of Cystic Fibrosis,ng cassette proteins. It is expressed in multiple tissues throughout the body, where it plays a key role in the regulation of ion transport across cell membranes in mucosal surfaces [1]. CFTR conducts chloride (Cl) and bicarbonate (HCO.), and it also appears to reduce sodium (Na) transport through i
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Monitoring and Evaluation of Patients with Cystic Fibrosis,early intervention have been realized. The era of newborn screening (NBS) has provided a wealth of information that has demonstrated the importance of optimal nutrition early in life. The prognosis of an individual patient is closely tied to his or her nutritional status and, therefore necessitates
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