Olaf Eickmeier
- CXCR1 and CXCR2 haplotypes synergistically modulate cystic fibrosis lung diseaseBy Michael S.D. Kormann, Andreas Hector, Veronica Marcos, Lauren E. Mays, Matthias Kappler, Thomas Illig, Norman Klopp, Sonja Zeilinger, Melanie Carevic, Nikolaus Rieber, Olaf Eickmeier, Stefan Zielen, Amit Gaggar, Barbara Moepps, Matthias Griese and Dominik HartlMichael S.D. KormannAndreas HectorVeronica MarcosLauren E. MaysMatthias KapplerThomas IlligNorman KloppSonja ZeilingerMelanie CarevicNikolaus RieberOlaf EickmeierStefan ZielenAmit GaggarBarbara MoeppsMatthias Griese
- TGFβ1 genotype in correlation to TGFβ1 induced sputum (IS) and serum in cystic fibrosis (CF)By Sabina Schmitt-Grohé, Felix Schreiner, Louisa van den Boom, Doris N'Gampolo, Olaf Eickmeier, Ralf Schubert, Ilse Broeckart, Stefan Zielen and Michael LentzeSabina Schmitt-Grohé1Children's Hospital Medical Center, University of Bonn, Bonn, GermanyFelix Schreiner1Children's Hospital Medical Center, University of Bonn, Bonn, GermanyLouisa van den Boom1Children's Hospital Medical Center, University of Bonn, Bonn, GermanyDoris N'Gampolo1Children's Hospital Medical Center, University of Bonn, Bonn, GermanyOlaf Eickmeier2Department of Pediatric Pulmonary, Goethe University Hospital, Frankfurt, GermanyRalf Schubert2Department of Pediatric Pulmonary, Goethe University Hospital, Frankfurt, GermanyIlse Broeckart1Children's Hospital Medical Center, University of Bonn, Bonn, GermanyStefan Zielen2Department of Pediatric Pulmonary, Goethe University Hospital, Frankfurt, GermanyMichael Lentze1Children's Hospital Medical Center, University of Bonn, Bonn, Germany
- Vocal cord dysfunction in adolescentsBy Johannes Schulze, Sarah Weber, Martin Rosewich, Olaf Eickmeier, Markus Rose and Stefan ZielenJohannes SchulzeDepartment of Allergy, Pulmonology and Cystic Fibrosis, Children's Hospital, Goethe-University, Frankfurt, GermanySarah WeberDepartment of Allergy, Pulmonology and Cystic Fibrosis, Children's Hospital, Goethe-University, Frankfurt, GermanyMartin RosewichDepartment of Allergy, Pulmonology and Cystic Fibrosis, Children's Hospital, Goethe-University, Frankfurt, GermanyOlaf EickmeierDepartment of Allergy, Pulmonology and Cystic Fibrosis, Children's Hospital, Goethe-University, Frankfurt, GermanyMarkus RoseDepartment of Allergy, Pulmonology and Cystic Fibrosis, Children's Hospital, Goethe-University, Frankfurt, GermanyStefan ZielenDepartment of Allergy, Pulmonology and Cystic Fibrosis, Children's Hospital, Goethe-University, Frankfurt, Germany
- Connexin 37 and Connexin 43 genotypes in correlation to cytokines in induced sputum and blood in cystic fibrosis (CF)By Olaf Eickmeier, Michael Ludwig, Felix Schreiner, Louisa van denBoom, Michael J. Lentze, Doris NGampolo, Ralf Schubert, Stefan Zielen and Sabina Schmitt-GroheOlaf Eickmeier2Pneumology, Allergy and Cystic Fibrosis, Children's Hospital, Goethe University, Frankfurt, GermanyMichael Ludwig3Clinical Chemistry and Clinical Pharmacology, University of Bonn, GermanyFelix Schreiner1Allgemeine Paediatrie, Zentrum fuer Kinderheilkunde des Universitaetsklinikum, Bonn, GermanyLouisa van denBoom1Allgemeine Paediatrie, Zentrum fuer Kinderheilkunde des Universitaetsklinikum, Bonn, GermanyMichael J. Lentze1Allgemeine Paediatrie, Zentrum fuer Kinderheilkunde des Universitaetsklinikum, Bonn, GermanyDoris NGampolo1Allgemeine Paediatrie, Zentrum fuer Kinderheilkunde des Universitaetsklinikum, Bonn, GermanyRalf Schubert3Clinical Chemistry and Clinical Pharmacology, University of Bonn, GermanyStefan Zielen3Clinical Chemistry and Clinical Pharmacology, University of Bonn, GermanySabina Schmitt-Grohe1Allgemeine Paediatrie, Zentrum fuer Kinderheilkunde des Universitaetsklinikum, Bonn, Germany
- Connexin 37 and connexin 43 genotypes in correlation to cytokines in induced sputum and blood in cystic fibrosis (CF)By Michael Ludwig, Olaf Eickmeier, Christina Smaczny, Felix Schreiner, Wilma Dubois, Doris NGampolo, Ralf Schubert, Stefan Zielen, Rainer Ganschow and Sabina Schmitt-GrohéMichael Ludwig2Institut für Klinische Biochemie und Klinische Pharmakologie, Universitätsklinikum Bonn, Bonn, GermanyOlaf Eickmeier3Christiane Herzog CF-Zentrum des Universitätsklinikum Frankfurt, Goethe-Universität, Frankfurt, GermanyChristina Smaczny3Christiane Herzog CF-Zentrum des Universitätsklinikum Frankfurt, Goethe-Universität, Frankfurt, GermanyFelix Schreiner1Abt. Allgemeine Pädiatrie, Zentrum für Kinderheilkunde des Universitätsklinikums Bonn, Bonn, GermanyWilma Dubois1Abt. Allgemeine Pädiatrie, Zentrum für Kinderheilkunde des Universitätsklinikums Bonn, Bonn, GermanyDoris NGampolo1Abt. Allgemeine Pädiatrie, Zentrum für Kinderheilkunde des Universitätsklinikums Bonn, Bonn, GermanyRalf Schubert3Christiane Herzog CF-Zentrum des Universitätsklinikum Frankfurt, Goethe-Universität, Frankfurt, GermanyStefan Zielen3Christiane Herzog CF-Zentrum des Universitätsklinikum Frankfurt, Goethe-Universität, Frankfurt, GermanyRainer Ganschow1Abt. Allgemeine Pädiatrie, Zentrum für Kinderheilkunde des Universitätsklinikums Bonn, Bonn, GermanySabina Schmitt-Grohé1Abt. Allgemeine Pädiatrie, Zentrum für Kinderheilkunde des Universitätsklinikums Bonn, Bonn, Germany
- Pirfenidone in diffuse parenchymal lung disease after stem cell transplantation of a patient with dyskeratosis congenitaBy Martin Rosewich, Olaf Eickmeier, Jonas Eckrich, Ralf Schubert and Stefan ZieenMartin Rosewich1Department of Pediatric Pulmonology, Allergy and Cystic fibrosis, Children's Hospital, Goethe-University, Frankfurt/M, GermanyOlaf Eickmeier1Department of Pediatric Pulmonology, Allergy and Cystic fibrosis, Children's Hospital, Goethe-University, Frankfurt/M, GermanyJonas Eckrich1Department of Pediatric Pulmonology, Allergy and Cystic fibrosis, Children's Hospital, Goethe-University, Frankfurt/M, GermanyRalf Schubert1Department of Pediatric Pulmonology, Allergy and Cystic fibrosis, Children's Hospital, Goethe-University, Frankfurt/M, GermanyStefan Zieen1Department of Pediatric Pulmonology, Allergy and Cystic fibrosis, Children's Hospital, Goethe-University, Frankfurt/M, Germany
- CXCR4+ granulocytes reflect fungal cystic fibrosis lung diseaseBy Melanie Carevic, Anurag Singh, Nikolaus Rieber, Olaf Eickmeier, Matthias Griese, Andreas Hector and Dominik HartlArticle | Published in 2015 in European Respiratory JournalMelanie Carevic1CF Centre, Dept of Pediatrics I, University of Tübingen, Tübingen, GermanyAnurag Singh1CF Centre, Dept of Pediatrics I, University of Tübingen, Tübingen, GermanyNikolaus Rieber1CF Centre, Dept of Pediatrics I, University of Tübingen, Tübingen, GermanyOlaf Eickmeier2Dept of Pediatric Pulmonology, Allergy and Cystic Fibrosis, Children's Hospital, Christiane Herzog CF-Center, Goethe University, Frankfurt, GermanyMatthias Griese3Dept of Pediatrics, Ludwig-Maximilians-University, Comprehensive Pneumology Center Munich, German Center for Lung Research (DZL), Munich, GermanyAndreas Hector1CF Centre, Dept of Pediatrics I, University of Tübingen, Tübingen, GermanyDominik Hartl1CF Centre, Dept of Pediatrics I, University of Tübingen, Tübingen, Germany
- CXCR4+ granulocytes reflect fungal cystic fibrosis lung diseaseBy Melanie Carevic, Anurag Singh, Nikolaus Rieber, Olaf Eickmeier, Matthias Griese, Andreas Hector and Dominik HartlMelanie Carevic1CF Centre, Dept of Pediatrics I, University of Tübingen, Tübingen, GermanyAnurag Singh1CF Centre, Dept of Pediatrics I, University of Tübingen, Tübingen, GermanyNikolaus Rieber1CF Centre, Dept of Pediatrics I, University of Tübingen, Tübingen, GermanyOlaf Eickmeier2Dept of Pediatric Pulmonology, Allergy and Cystic Fibrosis, Children's Hospital, Christiane Herzog CF-Center, Goethe University, Frankfurt, GermanyMatthias Griese3Dept of Pediatrics, Ludwig-Maximilians-University, Comprehensive Pneumology Center Munich, German Center for Lung Research (DZL), Munich, GermanyAndreas Hector1CF Centre, Dept of Pediatrics I, University of Tübingen, Tübingen, GermanyDominik Hartl1CF Centre, Dept of Pediatrics I, University of Tübingen, Tübingen, Germany
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