- Forty years experience with sweat chloride testing in the Prague CF Centre2002 | Central Library of Charles University, Second Faculty of Medicine
- Phenotypic characterisation of patients with intermediate sweat chloride values: towards validation of the European diagnostic algorithm for cystic fibrosis2009 | Publication without faculty affiliation
- A mutation in the cystic fibrosis transmembrane conductance regulator gene associated with elevated sweat chloride concentrations in the absence of cystic fibrosis1998 | Central Library of Charles University
- Failure to Thrive with Elevated Sweat Chloride Concentration:Susp. Cystic fibrosis X Nephrogen.Diab.Insip.Publication without faculty affiliation
- Human epididymis protein 4 (HE4) levels inversely correlate with lung function improvement (delta FEV1) in cystic fibrosis patients receiving ivacaftor treatment2019 | Second Faculty of Medicine
- Human epididymis protein 4 (HE4) plasma concentration inversely correlates with the improvement of cystic fibrosis lung disease in p.Phe508del-CFTR homozygous cases treated with the CFTR modulator lumacaftor/ivacaftor combination2023 | Second Faculty of Medicine
- Elexacaftor-tezacaftor-ivacaftor in patients with cystic fibrosis ineligible for clinical trials: a 24-week observational study2023 | Second Faculty of Medicine
- Cystic fibrosis transmembrane conductance regulator (CFTR) gene mutations in allergic bronchopulmonary aspergillosis1996 | Central Library of Charles University
- GLPG1837, a CFTR potentiator, in p.Gly551Asp (G551D)-CF patients: An open-label, single-arm, phase 2a study (SAPHIRA1)2019 | Second Faculty of Medicine
- European best practice guidelines for cystic fibrosis neonatal screening2009 | Second Faculty of Medicine
- Contemporary State of the Diagnosis of Cystic Fibrosis1999 | Second Faculty of Medicine
- CFTR activity is enhanced by the novel corrector GLPG2222, given with and without ivacaftor in two randomized trials2019 | Second Faculty of Medicine
- Clinical Phenotype and Genotype of Children with Borderline Sweat Test and Abnormal Nasal Epithelial Chloride Transport2010 | Second Faculty of Medicine
- Rectal organoid morphology analysis (ROMA) as a promising diagnostic tool in cystic fibrosis2021 | Second Faculty of Medicine
- Proper Interpretation of Elastase-1 Concentration in Stool: Experience of the Prague CF Centre2002 | Second Faculty of Medicine
- Diagnostics of cystic fibrosis in adults2016 | Second Faculty of Medicine, First Faculty of Medicine, Faculty of Physical Education and Sport, Faculty of Medicine in Pilsen, Faculty of Medicine in Hradec Králové
- Correction of CFTR function in intestinal organoids to guide treatment of Cystic Fibrosis2021 | Second Faculty of Medicine
- Case report of a Thai male cystic fibrosis patinet with the 1898+ 1G-->T splicing mutation in the CFTR gene: a review of East Asian cases. Mutations in brief no. 196. Online1998 | Second Faculty of Medicine
- Cystic fibrosis in adults +32014 | Second Faculty of Medicine
- Current options for diagnosing respiratory tract infections in children2012 | Second Faculty of Medicine
- Vanishing Lung Syndrome in a Cystic Fibrosis Patient2017 | Second Faculty of Medicine
- Laboratory biomarkers for lung disease severity and progression in cystic fibrosis2020 | Second Faculty of Medicine
- Assessment of Distinct Electrophysiological Parameters in Rectal Biopsies for the Choice of the Best Diagnosis/Prognosis Biomarkers for Cystic Fibrosis2020 | Second Faculty of Medicine
- Cystic fibrosis patients bearing both the common missense mutation GlyRIGHTWARDS ARROWAsp at codon 551 and the ΔF508 mutation are clinically indistinguishable from ΔF508 homozygotes, except for decreased risk of meconium ileus1992 | Second Faculty of Medicine
- Rectal Organoid Morphology Analysis (ROMA): A Diagnostic Assay in Cystic Fibrosis2022 | Second Faculty of Medicine
- Demographic characteristics, clinical and laboratory features, and the distribution of pathogenic variants in the CFTR gene in the Cypriot cystic fibrosis (CF) population demonstrate the utility of a national CF patient registry2021 | Second Faculty of Medicine
- Cystic fibrosis with exocrine pancreatic sufficiency2007 | Second Faculty of Medicine