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24. Personalized medicine for cystic fibrosis: establishing human model systems. Mou H; Brazauskas K; Rajagopal J Pediatr Pulmonol; 2015 Oct; 50 Suppl 40():S14-23. PubMed ID: 26335952 [TBL] [Abstract][Full Text] [Related]
25. Use of in vivo nasal transepithelial potential difference to evaluate efficacy in CF gene therapy phase I trials. Chinet TC Eur Respir J; 1994 Nov; 7(11):1917-20. PubMed ID: 7875259 [No Abstract] [Full Text] [Related]
26. [Lung function tests in cystic fibrosis as a means of guiding treatment]. Andersen HJ; Bjure J; Hjalmarson O; Kjellmer I Lakartidningen; 1976 Mar; 73(10):859-62. PubMed ID: 1256133 [No Abstract] [Full Text] [Related]
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40. Newborn screening for cystic fibrosis: an opportunity to improve care and outcomes. Campbell PW; White TB J Pediatr; 2005 Sep; 147(3 Suppl):S2-5. PubMed ID: 16202776 [No Abstract] [Full Text] [Related] [Previous] [Next] [New Search]