Works by Sommerburg, Olaf
Results: 55
Intestinal current measurement detects age-dependent differences in CFTR function in rectal epithelium.
- Published in:
- Frontiers in Pharmacology, 2025, p. 1, doi. 10.3389/fphar.2025.1537095
- By:
- Publication type:
- Article
The value of chest magnetic resonance imaging compared to chest radiographs with and without additional lung ultrasound in children with complicated pneumonia.
- Published in:
- PLoS ONE, 2020, v. 15, n. 3, p. 1, doi. 10.1371/journal.pone.0230252
- By:
- Publication type:
- Article
β‐Carotene cleavage products induce oxidative stress in vitro by impairing mitochondrial respiration.
- Published in:
- FASEB Journal, 2002, v. 16, n. 10, p. 1289, doi. 10.1096/fj.01-0765fje
- By:
- Publication type:
- Article
Pädiatrische chronische Rhinosinusitis.
- Published in:
- HNO, 2024, v. 72, n. 4, p. 250, doi. 10.1007/s00106-023-01405-8
- By:
- Publication type:
- Article
Longitudinal Magnetic Resonance Imaging of Changes in Lung Morphology and Perfusion in Children with Cystic Fibrosis from Infancy through Adolescence.
- Published in:
- Annals of the American Thoracic Society, 2025, v. 22, n. 1, p. 93, doi. 10.1513/AnnalsATS.202404-396OC
- By:
- Publication type:
- Article
Long-Term Impact of Lumacaftor/Ivacaftor Treatment on Cystic Fibrosis Disease Progression in Children 2–5 Years of Age Homozygous for F508del-CFTR : A Phase 2, Open-Label Clinical Trial.
- Published in:
- Annals of the American Thoracic Society, 2024, v. 21, n. 11, p. 1550, doi. 10.1513/AnnalsATS.202402-201OC
- By:
- Publication type:
- Article
Magnetic Resonance Imaging of Pulmonary and Paranasal Sinus Abnormalities in Children with Primary Ciliary Dyskinesia Compared to Children with Cystic Fibrosis.
- Published in:
- Annals of the American Thoracic Society, 2024, v. 21, n. 3, p. 438, doi. 10.1513/AnnalsATS.202305-453OC
- By:
- Publication type:
- Article
Elexacaftor/Tezacaftor/Ivacaftor Improves Bronchial Artery Dilatation Detected by Magnetic Resonance Imaging in Patients with Cystic Fibrosis.
- Published in:
- Annals of the American Thoracic Society, 2023, v. 20, n. 11, p. 1595, doi. 10.1513/AnnalsATS.202302-168OC
- By:
- Publication type:
- Article
Effects of Lumacaftor/Ivacaftor on Cystic Fibrosis Disease Progression in Children 2 through 5 Years of Age Homozygous for F508del-CFTR: A Phase 2 Placebo-controlled Clinical Trial.
- Published in:
- Annals of the American Thoracic Society, 2023, v. 20, n. 8, p. 1144, doi. 10.1513/AnnalsATS.202208-684OC
- By:
- Publication type:
- Article
Longitudinal Magnetic Resonance Imaging Detects Onset and Progression of Chronic Rhinosinusitis from Infancy to School Age in Cystic Fibrosis.
- Published in:
- Annals of the American Thoracic Society, 2023, v. 20, n. 5, p. 687, doi. 10.1513/AnnalsATS.202209-763OC
- By:
- Publication type:
- Article
Effects of Lumacaftor-Ivacaftor on Lung Clearance Index, Magnetic Resonance Imaging, and Airway Microbiome in Phe508del Homozygous Patients with Cystic Fibrosis.
- Published in:
- 2021
- By:
- Publication type:
- journal article
Magnetic Resonance Imaging Detects Chronic Rhinosinusitis in Infants and Preschool Children with Cystic Fibrosis.
- Published in:
- 2020
- By:
- Publication type:
- journal article
Changes in Microbiome Dominance Are Associated With Declining Lung Function and Fluctuating Inflammation in People With Cystic Fibrosis.
- Published in:
- Frontiers in Microbiology, 2022, v. 13, p. 1, doi. 10.3389/fmicb.2022.885822
- By:
- Publication type:
- Article
Risk Factors for Complicated Lymphadenitis Caused by Nontuberculous Mycobacteria in Children.
- Published in:
- 2020
- By:
- Publication type:
- journal article
Patient experiences of interprofessional collaboration and intersectoral communication in rare disease healthcare in Germany – a mixed-methods study.
- Published in:
- Orphanet Journal of Rare Diseases, 2024, v. 19, n. 1, p. 1, doi. 10.1186/s13023-024-03207-9
- By:
- Publication type:
- Article
Airway Mucus Obstruction Triggers Macrophage Activation and Matrix Metalloproteinase 12-Dependent Emphysema.
- Published in:
- American Journal of Respiratory Cell & Molecular Biology, 2014, v. 51, n. 5, p. 709, doi. 10.1165/rcmb.2013-0407OC
- By:
- Publication type:
- Article
Effects of Elexacaftor/Tezacaftor/Ivacaftor Therapy on Lung Clearance Index and Magnetic Resonance Imaging in Patients with Cystic Fibrosis and One or Two Alleles.
- Published in:
- American Journal of Respiratory & Critical Care Medicine, 2022, v. 206, n. 3, p. 311, doi. 10.1164/rccm.202201-0219OC
- By:
- Publication type:
- Article
Effects of Elexacaftor/Tezacaftor/Ivacaftor Therapy on CFTR Function in Patients with Cystic Fibrosis and One or Two Alleles.
- Published in:
- 2022
- By:
- Publication type:
- journal article
Effects of Elexacaftor/Tezacaftor/Ivacaftor Therapy on CFTR Function in Patients with Cystic Fibrosis and One or Two F508del Alleles.
- Published in:
- American Journal of Respiratory & Critical Care Medicine, 2022, v. 205, n. 5, p. E1, doi. 10.1164/rccm.202110-2249oc
- By:
- Publication type:
- Article
Magnetic Resonance Imaging Detects Progression of Lung Disease and Impact of Newborn Screening in Preschool Children with Cystic Fibrosis.
- Published in:
- American Journal of Respiratory & Critical Care Medicine, 2021, v. 204, n. 8, p. E1, doi. 10.1164/rccm.202102-0278oc
- By:
- Publication type:
- Article
Magnetic Resonance Imaging Detects Progression of Lung Disease and Impact of Newborn Screening in Preschool Children with Cystic Fibrosis.
- Published in:
- 2021
- By:
- Publication type:
- journal article
Abdominelle Manifestationen bei Mukoviszidose: Klinische Übersicht.
- Published in:
- Der Radiologe, 2020, v. 60, n. 9, p. 781, doi. 10.1007/s00117-020-00729-8
- By:
- Publication type:
- Article
Ten years of chest MRI for patients with cystic fibrosis: Translation from the bench to clinical routine.
- Published in:
- Der Radiologe, 2019, v. 59, p. 10, doi. 10.1007/s00117-019-0553-2
- By:
- Publication type:
- Article
Update Mukoviszidose: Vom Neugeborenenscreening zur kausalen Therapie.
- Published in:
- Die Radiologie, 2022, v. 62, n. 11, p. 981, doi. 10.1007/s00117-022-01076-6
- By:
- Publication type:
- Article
Automated lung segmentation on chest MRI in children with cystic fibrosis.
- Published in:
- Frontiers in Medicine, 2024, p. 1, doi. 10.3389/fmed.2024.1401473
- By:
- Publication type:
- Article
The association of COVID-19 pandemic with the increase of sinogenic and otogenic intracranial infections in children: a 10-year retrospective comparative single-center study.
- Published in:
- Neurosurgical Review, 2024, v. 47, n. 1, p. 1, doi. 10.1007/s10143-024-02442-9
- By:
- Publication type:
- Article
Echo Time‐Dependence of Observed Lung T<sub>1</sub> in Patients With Cystic Fibrosis and Correlation With Clinical Metrics.
- Published in:
- Journal of Magnetic Resonance Imaging, 2020, v. 52, n. 6, p. 1645, doi. 10.1002/jmri.27271
- By:
- Publication type:
- Article
German newborn screening for Cystic fibrosis: Parental perspectives and suggestions for improvements.
- Published in:
- Pediatric Pulmonology, 2023, v. 58, n. 3, p. 844, doi. 10.1002/ppul.26263
- By:
- Publication type:
- Article
Rescue of respiratory failure in pulmonary alveolar proteinosis due to pathogenic MARS1 variants.
- Published in:
- Pediatric Pulmonology, 2020, v. 55, n. 11, p. 3057, doi. 10.1002/ppul.25031
- By:
- Publication type:
- Article
Carotenoid oxidative degradation products inhibit Na<sup>+</sup>-K<sup>+</sup>-ATPase.
- Published in:
- Free Radical Research, 2000, v. 33, n. 4, p. 427, doi. 10.1080/10715760000300961
- By:
- Publication type:
- Article
Carotenoid supply in breast-fed and formula-fed neonates.
- Published in:
- European Journal of Pediatrics, 2000, v. 159, n. 1/2, p. 86, doi. 10.1007/PL00013811
- By:
- Publication type:
- Article
Proteasomal degradation of β-carotene metabolite—Modified proteins.
- Published in:
- Biofactors, 2009, v. 35, n. 5, p. 449, doi. 10.1002/biof.59
- By:
- Publication type:
- Article
HNE and Further Lipid Peroxidation Products.
- Published in:
- Biofactors, 2005, v. 24, n. 1-4, p. 1, doi. 10.1002/biof.5520240101
- By:
- Publication type:
- Article
Localization of carotenoids in different eye tissues.
- Published in:
- Biofactors, 2000, v. 11, n. 1/2, p. 3, doi. 10.1002/biof.5520110102
- By:
- Publication type:
- Article
Lycopene and Beta-carotene decompose more rapidly than lutein and zeaxanthin upon exposure...
- Published in:
- Biofactors, 1999, v. 10, n. 2/3, p. 105, doi. 10.1002/biof.5520100204
- By:
- Publication type:
- Article
Multiple Breath Washout Is Feasible in the Clinical Setting and Detects Abnormal Lung Function in Infants and Young Children with Cystic Fibrosis.
- Published in:
- Respiration, 2014, v. 87, n. 5, p. 357, doi. 10.1159/000357075
- By:
- Publication type:
- Article
Increased Inflammatory Markers Detected in Nasal Lavage Correlate with Paranasal Sinus Abnormalities at MRI in Adolescent Patients with Cystic Fibrosis.
- Published in:
- Antioxidants, 2021, v. 10, n. 9, p. 1412, doi. 10.3390/antiox10091412
- By:
- Publication type:
- Article
CFTR Modulator Therapy with Lumacaftor/Ivacaftor Alters Plasma Concentrations of Lipid-Soluble Vitamins A and E in Patients with Cystic Fibrosis.
- Published in:
- Antioxidants, 2021, v. 10, n. 3, p. 483, doi. 10.3390/antiox10030483
- By:
- Publication type:
- Article
Effects of lumacaftor--ivacaftor therapy on cystic fibrosis transmembrane conductance regulator function in F508del homozygous patients with cystic fibrosis aged 2-11 years.
- Published in:
- Frontiers in Pharmacology, 2023, p. 1, doi. 10.3389/fphar.2023.1188051
- By:
- Publication type:
- Article
Long-term effects of lumacaftor/ivacaftor on paranasal sinus abnormalities in children with cystic fibrosis detected with magnetic resonance imaging.
- Published in:
- Frontiers in Pharmacology, 2023, v. 14, p. 1, doi. 10.3389/fphar.2023.1161891
- By:
- Publication type:
- Article
Supplementation with Red Palm Oil Increases β-Carotene and Vitamin A Blood Levels in Patients with Cystic Fibrosis.
- Published in:
- Mediators of Inflammation, 2015, v. 2015, p. 1, doi. 10.1155/2015/817127
- By:
- Publication type:
- Article
Initial evaluation of a biochemical cystic fibrosis newborn screening by sequential analysis of immunoreactive trypsinogen and pancreatitis-associated protein (IRT/PAP) as a strategy that does not involve DNA testing in a Northern European population.
- Published in:
- Journal of Inherited Metabolic Disease, 2010, v. 33, p. 263, doi. 10.1007/s10545-010-9174-7
- By:
- Publication type:
- Article
Influence of Season, Storage Temperature and Time of Sample Collection in Pancreatitis-Associated Protein-Based Algorithms for Newborn Screening for Cystic Fibrosis.
- Published in:
- International Journal of Neonatal Screening (IJNS), 2024, v. 10, n. 1, p. 5, doi. 10.3390/ijns10010005
- By:
- Publication type:
- Article
Cystic Fibrosis Cases Missed by Newborn Bloodspot Screening—Towards a Consistent Definition and Data Acquisition.
- Published in:
- International Journal of Neonatal Screening (IJNS), 2023, v. 9, n. 4, p. 65, doi. 10.3390/ijns9040065
- By:
- Publication type:
- Article
Lutein and zeaxanthin are associated with photoreceptors in thehuman retina.
- Published in:
- Current Eye Research, 1999, v. 19, n. 6, doi. 10.1076/ceyr.19.6.491.5276
- By:
- Publication type:
- Article
Five years of experience with biochemical cystic fibrosis newborn screening based on IRT/PAP in Germany.
- Published in:
- Pediatric Pulmonology, 2015, v. 50, n. 7, p. 655, doi. 10.1002/ppul.23190
- By:
- Publication type:
- Article
Implementing a tracking system for confirmatory diagnostic results after positive newborn screening for cystic fibrosis—implications for process quality and patient care.
- Published in:
- European Journal of Pediatrics, 2021, v. 180, n. 4, p. 1145, doi. 10.1007/s00431-020-03849-4
- By:
- Publication type:
- Article
Homozygous CFTR mutation M348K in a boy with respiratory symptoms and failure to thrive. Disease-causing mutation or benign alteration?
- Published in:
- European Journal of Pediatrics, 2012, v. 171, n. 7, p. 1039, doi. 10.1007/s00431-012-1672-1
- By:
- Publication type:
- Article
Therapeutic Drug Monitoring of Elexacaftor, Tezacaftor, and Ivacaftor in Adult People with Cystic Fibrosis.
- Published in:
- Journal of Personalized Medicine, 2024, v. 14, n. 10, p. 1065, doi. 10.3390/jpm14101065
- By:
- Publication type:
- Article
A Volatile and Dynamic Longitudinal Microbiome Is Associated With Less Reduction in Lung Function in Adolescents With Cystic Fibrosis.
- Published in:
- Frontiers in Cellular & Infection Microbiology, 2021, v. 11, p. 1, doi. 10.3389/fcimb.2021.763121
- By:
- Publication type:
- Article