The Changing Face of Cystic Fibrosis and Its Implications for Screening von Naehrlich, Lutz

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Risk factors for respiratory Aspergillus fumigatus in German Cystic Fibrosis patients and impact on lung function von Düesberg, Uta, Wosniok, Julia, Naehrlich, Lutz, Eschenhagen, Patience, Schwarz, Carsten

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Use of elexacaftor/tezacaftor/ivacaftor leads to changes in detection frequencies of Staphylococcus aureus and Pseudomonas aeruginosa dependent on age and lung function in people w... von Dittrich, Anna-Maria, Sieber, Sarah, Naehrlich, Lutz, Burkhart, Manuel, Hafkemeyer, Sylvia, Tümmler, Burkhard

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Assessment of pathologic increase in liver stiffness enables earlier diagnosis of CFLD: Results from a prospective longitudinal cohort study von Klotter, Victoria, Gunchick, Caroline, Siemers, Enno, Rath, Timo, Hudel, Helge, Naehrlich, Lutz, Roderfeld, Martin, Roeb, Elke

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Elexacaftor-Tezacaftor-Ivacaftor Treatment Reduces Abdominal Symptoms in Cystic Fibrosis-Early results Obtained With the CF-Specific CFAbd-Score von Mainz, Jochen G, Zagoya, Carlos, Polte, Louise, Naehrlich, Lutz, Sasse, Lenny, Eickmeier, Olaf, Smaczny, Christina, Barucha, Anton, Bechinger, Lilith, Duckstein, Franziska, Kurzidim, Ludwik, Eschenhagen, Patience, Caley, Laura, Peckham, Daniel, Schwarz, Carsten

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Epidemiological trends in nontuberculous mycobacterial infection among people with cystic fibrosis in Germany von Steindor, Mathis, Hafkemeyer, Sylvia, Ruckes, Christian, Stehling, Florian, Naehrlich, Lutz, Ringshausen, Felix C

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Cross-sectional seroprevalence surveys of SARS-CoV-2 antibodies in children in Germany, June 2020 to May 2021 von Sorg, Anna-Lisa, Bergfeld, Leon, Jank, Marietta, Corman, Victor, Semmler, Ilia, Goertz, Anna, Beyerlein, Andreas, Verjans, Eva, Wagner, Norbert, Von Bernuth, Horst, Lander, Fabian, Weil, Katharina, Hufnagel, Markus, Spiekerkoetter, Ute, Chao, Cho-Ming, Naehrlich, Lutz, Muntau, Ania Carolina, Schulze-Sturm, Ulf, Hansen, Gesine, Wetzke, Martin, Jung, Anna-Maria, Niehues, Tim, Fricke-Otto, Susanne, Von Both, Ulrich, Huebner, Johannes, Behrends, Uta, Liese, Johannes G., Schwerk, Christian, Drosten, Christian, Von Kries, Ruediger, Schroten, Horst

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Hermansky-Pudlak syndrome type 2 manifests with fibrosing lung disease early in childhood von Hengst, Meike, Naehrlich, Lutz, Mahavadi, Poornima, Grosse-Onnebrink, Joerg, Terheggen-Lagro, Suzanne, Skanke, Lars Høsøien, Schuch, Luise A, Brasch, Frank, Guenther, Andreas, Reu, Simone, Ley-Zaporozhan, Julia, Griese, Matthias

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Personalized medicine with drugs targeting the underlying protein defect in cystic fibrosis: is monitoring of treatment response necessary? von Niedermayr, Katharina, Gasser, Verena, Rueckes-Nilges, Claudia, Appelt, Dorothea, Eder, Johannes, Fuchs, Teresa, Naehrlich, Lutz, Ellemunter, Helmut

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High variability in oral glucose tolerance among 1,128 patients with cystic fibrosis: a multicenter screening study von Scheuing, Nicole, Holl, Reinhard W, Dockter, Gerd, Hermann, Julia M, Junge, Sibylle, Koerner-Rettberg, Cordula, Naehrlich, Lutz, Smaczny, Christina, Staab, Doris, Thalhammer, Gabriela, van Koningsbruggen-Rietschel, Silke, Ballmann, Manfred

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Have courage in using nasal potential difference for diagnostic decisions and clinical research von Naehrlich, Lutz

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Corrigendum: Elexacaftor-Tezacaftor-Ivacaftor treatment reduces abdominal symptoms in cystic fibrosis-early results obtained with the CF-specific CFAbd-Score von Mainz, Jochen G, Zagoya, Carlos, Polte, Louise, Naehrlich, Lutz, Sasse, Lenny, Eickmeier, Olaf, Smaczny, Christina, Barucha, Anton, Bechinger, Lilith, Duckstein, Franziska, Kurzidim, Ludwik, Eschenhagen, Patience, Caley, Laura, Peckham, Daniel, Schwarz, Carsten

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Serine Proteases Degrade Airway Mucins in Cystic Fibrosis von HENKE, Markus O, JOHN, Gerrit, RHEINECK, Christina, CHILLAPPAGARI, Shashi, NAEHRLICH, Lutz, RUBIN, Bruce K

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Identification of neutrophil activation markers as novel surrogate markers of CF lung disease von Rath, Timo, Zwaschka, Lisa, Hage, Lisa, Kügler, Marion, Menendez, Katrin, Naehrlich, Lutz, Schulz, Richard, Roderfeld, Martin, Roeb, Elke

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Serum proteome profiling identifies novel and powerful markers of cystic fibrosis liver disease von Rath, Timo, Hage, Lisa, Kügler, Marion, Menendez Menendez, Katrin, Zachoval, Reinhart, Naehrlich, Lutz, Schulz, Richard, Roderfeld, Martin, Roeb, Elke

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Diabetes in cystic fibrosis: multicenter screening results based on current guidelines von Scheuing, Nicole, Holl, Reinhard W, Dockter, Gerd, Fink, Katharina, Junge, Sibylle, Naehrlich, Lutz, Smaczny, Christina, Staab, Doris, Thalhammer, Gabriela, van Koningsbruggen-Rietschel, Silke, Ballmann, Manfred

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Cystic fibrosis transmembrane conductance regulator biomarkers in ‘real life’: can we evaluate individual efficacy of cystic fibrosis transmembrane conductance regulator therapy?... von van Koningsbruggen-Rietschel, Silke, Naehrlich, Lutz

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Multicentre feasibility of multiple-breath washout in preschool children with cystic fibrosis and other lung diseases von Stahl, Mirjam, Joachim, Cornelia, Kirsch, Ines, Uselmann, Tatjana, Yu, Yin, Alfeis, Nadine, Berger, Christiane, Minso, Rebecca, Rudolf, Isa, Stolpe, Cornelia, Bovermann, Xenia, Liboschik, Lena, Steinmetz, Alena, Tennhardt, Dunja, Dörfler, Friederike, Röhmel, Jobst, Unorji-Frank, Klaudia, Rückes-Nilges, Claudia, von Stoutz, Bianca, Naehrlich, Lutz, Kopp, Matthias V, Dittrich, Anna-Maria, Sommerburg, Olaf, Mall, Marcus A

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Risk factors for forced expiratory volume in 1 s decline in European patients with cystic fibrosis: data from the European Cystic Fibrosis Society Patient Registry von Hatziagorou, Elpis, Fieuws, Steffen, Orenti, Annalisa, Naehrlich, Lutz, Krivec, Uros, Mei-Zahav, Meir, Jung, Andreas, De Boeck, Kris

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Comparison of diagnostic data after introduction of cystic fibrosis screening in newborns in Germany von Nährlich, Lutz, Brockow, Inken

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