New clinical diagnostic procedures for cystic fibrosis in Europe von De Boeck, Christiane, Derichs, N, Fajac, I, de Jonge, H.R, Bronsveld, I, Sermet, I, Vermeulen, François, Sheppard, D.N, Cuppens Harry, Harry, Hug, M, Melotti, P, Middleton, P.G, Wilschanski, M, ECFS Diagnostic Network Working Group, EuroCareCF WP3 Group on CF diagnosis

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New clinical diagnostic procedures for cystic fibrosis in Europe von De Boeck, K, Derichs, N, Fajac, I, de Jonge, H.R, Bronsveld, I, Sermet, I, Vermeulen, F, Sheppard, D.N, Cuppens, H, Hug, M, Melotti, P, Middleton, P.G, Wilschanski, M

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Comparison of Nasal Potential Difference and Intestinal Current Measurements as Surrogate Markers for CFTR Function von Wilschanski, Michael, Yaakov, Yasmin, Omari, Ibrahim, Zaman, Munir, Martin, Camilia R., Cohen‐Cymberknoh, Malena, Shoseyov, David, Kerem, Eitan, Dasilva, Deborah, Sheth, Sunil, Uluer, Ahmet, O'Sullivan, Brian P., Freedman, Steven

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A Clinical and Molecular Survey of 62 Cystic Fibrosis Patients from Umbria (Central Italy) Disclosing a High Frequency (2.4%) of the 2184insA Allele: Implications for Screening von Prontera, Paolo, Isidori, Ilenia, Mencarini, Valeria, Pennoni, Guido, Mencarelli, Amedea, Stangoni, Gabriela, Di Cara, Giuseppe, Verrotti, Alberto

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Individualized medicine using intestinal responses to CFTR potentiators and correctors von Beekman, Jeffrey M.

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Functional analysis of the p.[Arg74Trp;Val201Met;Asp1270Asn]/p.Phe508del CFTR mutation genotype in human native colon von Schucht, Sylvia, Minso, Rebecca, Lex, Christiane, Reiss, Jochen, Stanke, Frauke, Tamm, Stephanie, van Barneveld, Andrea, Tümmler, Burkhard

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