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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書目名稱Handbook of Cystic Fibrosis影響因子(影響力)




書目名稱Handbook of Cystic Fibrosis影響因子(影響力)學(xué)科排名




書目名稱Handbook of Cystic Fibrosis網(wǎng)絡(luò)公開度




書目名稱Handbook of Cystic Fibrosis網(wǎng)絡(luò)公開度學(xué)科排名




書目名稱Handbook of Cystic Fibrosis被引頻次




書目名稱Handbook of Cystic Fibrosis被引頻次學(xué)科排名




書目名稱Handbook of Cystic Fibrosis年度引用




書目名稱Handbook of Cystic Fibrosis年度引用學(xué)科排名




書目名稱Handbook of Cystic Fibrosis讀者反饋




書目名稱Handbook of Cystic Fibrosis讀者反饋學(xué)科排名

EPT

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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Synchronism

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commodity

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

使人煩燥

詞匯記憶方法

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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