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Multicentre feasibility of multiple-breath washout in preschool children with cystic fibrosis and other lung diseases.
ERJ Open Res. 2020 Oct 26;6(4):00408-2020. doi: 10.1183/23120541.00408-2020. eCollection 2020 Oct.
ERJ Open Res. 2020.
PMID: 33263048
Free PMC article.
Intestinal current measurement and nasal potential difference to make a diagnosis of cases with inconclusive CFTR genetics and sweat test.
Minso R, Schulz A, Dopfer C, Alfeis N, Barneveld AV, Makartian-Gyulumyan L, Hansen G, Junge S, Müller C, Ringshausen FCC, Sauer-Heilborn A, Stanke F, Stolpe C, Tamm S, Welte T, Dittrich AM, Tümmler B.
Minso R, et al. Among authors: alfeis n.
BMJ Open Respir Res. 2020 Oct;7(1):e000736. doi: 10.1136/bmjresp-2020-000736.
BMJ Open Respir Res. 2020.
PMID: 33020115
Free PMC article.
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Clinical presentation and basic defect of the CFTR genotype p.Phe508del / p.Arg117His in a mother and her monozygous twin daughters.
Lex C, Minso R, Alfeis N, Rosewich H, Schucht S, Tümmler B.
Lex C, et al. Among authors: alfeis n.
J Cyst Fibros. 2022 Mar;21(2):375-377. doi: 10.1016/j.jcf.2021.08.018. Epub 2021 Sep 4.
J Cyst Fibros. 2022.
PMID: 34489188
Free article.
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