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Urinary acid mucopolysaccharides in cystic fibrosis.
Constantopoulos G, Dekaban AS, Lapey A, di Sant'Agnese PA. Constantopoulos G, et al. Among authors: lapey a. J Pediatr. 1971 May;78(5):806-11. doi: 10.1016/s0022-3476(71)80351-7. J Pediatr. 1971. PMID: 4253145 No abstract available.
Nutrient status of adults with cystic fibrosis.
Gordon CM, Anderson EJ, Herlyn K, Hubbard JL, Pizzo A, Gelbard R, Lapey A, Merkel PA. Gordon CM, et al. Among authors: lapey a. J Am Diet Assoc. 2007 Dec;107(12):2114-9. doi: 10.1016/j.jada.2007.09.005. J Am Diet Assoc. 2007. PMID: 18060897 Free PMC article.
Safety, pharmacokinetics, and pharmacodynamics of ivacaftor in patients aged 2-5 years with cystic fibrosis and a CFTR gating mutation (KIWI): an open-label, single-arm study.
Davies JC, Cunningham S, Harris WT, Lapey A, Regelmann WE, Sawicki GS, Southern KW, Robertson S, Green Y, Cooke J, Rosenfeld M; KIWI Study Group. Davies JC, et al. Among authors: lapey a. Lancet Respir Med. 2016 Feb;4(2):107-15. doi: 10.1016/S2213-2600(15)00545-7. Epub 2016 Jan 21. Lancet Respir Med. 2016. PMID: 26803277 Free PMC article. Clinical Trial.
51 results