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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: tamm s. 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.
Changes in cystic fibrosis transmembrane conductance regulator protein expression prior to and during elexacaftor-tezacaftor-ivacaftor therapy.
Stanke F, Pallenberg ST, Tamm S, Hedtfeld S, Eichhorn EM, Minso R, Hansen G, Welte T, Sauer-Heilborn A, Ringshausen FC, Junge S, Tümmler B, Dittrich AM. Stanke F, et al. Among authors: tamm s. Front Pharmacol. 2023 Jan 27;14:1114584. doi: 10.3389/fphar.2023.1114584. eCollection 2023. Front Pharmacol. 2023. PMID: 36778025 Free PMC article.
Genes that determine immunology and inflammation modify the basic defect of impaired ion conductance in cystic fibrosis epithelia.
Stanke F, Becker T, Kumar V, Hedtfeld S, Becker C, Cuppens H, Tamm S, Yarden J, Laabs U, Siebert B, Fernandez L, Macek M Jr, Radojkovic D, Ballmann M, Greipel J, Cassiman JJ, Wienker TF, Tümmler B. Stanke F, et al. Among authors: tamm s. J Med Genet. 2011 Jan;48(1):24-31. doi: 10.1136/jmg.2010.080937. Epub 2010 Sep 12. J Med Genet. 2011. PMID: 20837493 Free PMC article.
147 results