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Magnetic Resonance Imaging Detects Changes in Structure and Perfusion, and Response to Therapy in Early Cystic Fibrosis Lung Disease

American journal of respiratory and critical care medicine, 2014-04, Vol.189 (8), p.956-965

2014

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Diagnosis of Cystic Fibrosis in Screened Populations

The Journal of pediatrics, 2017-02, Vol.181, p.S33-S44.e2

2017

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Implementing a tracking system for confirmatory diagnostic results after positive newborn screening for cystic fibrosis—implications for process quality and patient care

European journal of pediatrics, 2021-04, Vol.180 (4), p.1145-1155

2021

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Pancreatitis-Associated Protein in Neonatal Screening for Cystic Fibrosis: Strengths and Weaknesses

International journal of neonatal screening, 2020-06, Vol.6 (2), p.28-28

2020

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The value of chest magnetic resonance imaging compared to chest radiographs with and without additional lung ultrasound in children with complicated pneumonia

PloS one, 2020, Vol.15 (3), p.e0230252-e0230252

2020

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Airway mucus obstruction triggers macrophage activation and matrix metalloproteinase 12-dependent emphysema

American journal of respiratory cell and molecular biology, 2014-11, Vol.51 (5), p.709-720

2014

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Patient experiences of interprofessional collaboration and intersectoral communication in rare disease healthcare in Germany - a mixed-methods study

Orphanet journal of rare diseases, 2024-05, Vol.19 (1), p.197-197, Article 197

2024

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Changes in Microbiome Dominance Are Associated With Declining Lung Function and Fluctuating Inflammation in People With Cystic Fibrosis

Frontiers in microbiology, 2022-05, Vol.13, p.885822-885822

2022

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Mukoviszidose — immer bessere Perspektive durch lebenslange adäquate Behandlung

Pneumo news, 2019-02, Vol.11 (1), p.32-40

Sommerburg, Olaf

2019

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Effects of lumacaftor-ivacaftor therapy on cystic fibrosis transmembrane conductance regulator function in F508del homozygous patients with cystic fibrosis aged 2-11 years

Frontiers in pharmacology, 2023-05, Vol.14, p.1188051-1188051

2023

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Long-term effects of lumacaftor/ivacaftor on paranasal sinus abnormalities in children with cystic fibrosis detected with magnetic resonance imaging

Frontiers in pharmacology, 2023-04, Vol.14, p.1161891-1161891

2023

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Risk Factors for Complicated Lymphadenitis Caused by Nontuberculous Mycobacteria in Children

Emerging infectious diseases, 2020-03, Vol.26 (3), p.579-586

2020

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A Volatile and Dynamic Longitudinal Microbiome Is Associated With Less Reduction in Lung Function in Adolescents With Cystic Fibrosis

Frontiers in cellular and infection microbiology, 2021-12, Vol.11, p.763121-763121

2021

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Update on cystic fibrosis : From neonatal screening to causal treatment

Radiologie (Heidelberg, Germany), 2022-11, Vol.62 (11), p.981-994

2022

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Update Mukoviszidose: Vom Neugeborenenscreening zur kausalen Therapie

Die Radiologie, 2022-11, Vol.62 (11), p.981-994

2022

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CFTR Modulator Therapy with Lumacaftor/Ivacaftor Alters Plasma Concentrations of Lipid-Soluble Vitamins A and E in Patients with Cystic Fibrosis

Antioxidants, 2021-03, Vol.10 (3), p.483

2021

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Sicherung der Atemwege des Neugeborenen bei beidseitiger Choanalatresie: Unverzügliche Atemwegssicherung, aber nicht in jedem Fall per Intubation

Monatsschrift Kinderheilkunde, 2019-08, Vol.167 (8), p.729-730

2019

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Increased Inflammatory Markers Detected in Nasal Lavage Correlate with Paranasal Sinus Abnormalities at MRI in Adolescent Patients with Cystic Fibrosis

Antioxidants, 2021-09, Vol.10 (9), p.1412

2021

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Cystic Fibrosis Cases Missed by Newborn Bloodspot Screening-Towards a Consistent Definition and Data Acquisition

International journal of neonatal screening, 2023-11, Vol.9 (4), p.65

2023

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Magnetic resonance imaging detects onset and association with lung disease severity of bronchial artery dilatation in cystic fibrosis

ERJ open research, 2023-03, Vol.9 (2), p.473

2023

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TRACK-CF prospective cohort study: Understanding early cystic fibrosis lung disease

Frontiers in medicine, 2023-01, Vol.9, p.1034290-1034290

2023

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Pädiatrische chronische Rhinosinusitis

HNO, 2024-04, Vol.72 (4), p.250-256

2024

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Long-Term Outcome After External Tracheal Stabilization Due to Congenital Tracheal Instability

The Annals of thoracic surgery, 2010-03, Vol.89 (3), p.918-925

2010

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Supplementation with Red Palm Oil Increases β-Carotene and Vitamin A Blood Levels in Patients with Cystic Fibrosis

Mediators of Inflammation, 2015-01, Vol.2015, p.817127-7

2015

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Magnetic Resonance Imaging Detects Changes in Structure and Perfusion, and Response to Therapy in Early Cystic Fibrosis Lung Disease

Diagnosis of Cystic Fibrosis in Screened Populations

Implementing a tracking system for confirmatory diagnostic results after positive newborn screening for cystic fibrosis—implications for process quality and patient care

Pancreatitis-Associated Protein in Neonatal Screening for Cystic Fibrosis: Strengths and Weaknesses

The value of chest magnetic resonance imaging compared to chest radiographs with and without additional lung ultrasound in children with complicated pneumonia

Airway mucus obstruction triggers macrophage activation and matrix metalloproteinase 12-dependent emphysema

Patient experiences of interprofessional collaboration and intersectoral communication in rare disease healthcare in Germany - a mixed-methods study

Changes in Microbiome Dominance Are Associated With Declining Lung Function and Fluctuating Inflammation in People With Cystic Fibrosis

Mukoviszidose — immer bessere Perspektive durch lebenslange adäquate Behandlung

Effects of lumacaftor-ivacaftor therapy on cystic fibrosis transmembrane conductance regulator function in F508del homozygous patients with cystic fibrosis aged 2-11 years

Long-term effects of lumacaftor/ivacaftor on paranasal sinus abnormalities in children with cystic fibrosis detected with magnetic resonance imaging

Risk Factors for Complicated Lymphadenitis Caused by Nontuberculous Mycobacteria in Children

A Volatile and Dynamic Longitudinal Microbiome Is Associated With Less Reduction in Lung Function in Adolescents With Cystic Fibrosis

Update on cystic fibrosis : From neonatal screening to causal treatment

Update Mukoviszidose: Vom Neugeborenenscreening zur kausalen Therapie

CFTR Modulator Therapy with Lumacaftor/Ivacaftor Alters Plasma Concentrations of Lipid-Soluble Vitamins A and E in Patients with Cystic Fibrosis

Sicherung der Atemwege des Neugeborenen bei beidseitiger Choanalatresie: Unverzügliche Atemwegssicherung, aber nicht in jedem Fall per Intubation

Increased Inflammatory Markers Detected in Nasal Lavage Correlate with Paranasal Sinus Abnormalities at MRI in Adolescent Patients with Cystic Fibrosis

Cystic Fibrosis Cases Missed by Newborn Bloodspot Screening-Towards a Consistent Definition and Data Acquisition

Magnetic resonance imaging detects onset and association with lung disease severity of bronchial artery dilatation in cystic fibrosis

TRACK-CF prospective cohort study: Understanding early cystic fibrosis lung disease

Multicentre feasibility of multiple-breath washout in preschool children with cystic fibrosis and other lung diseases

Pädiatrische chronische Rhinosinusitis

Long-Term Outcome After External Tracheal Stabilization Due to Congenital Tracheal Instability

Supplementation with Red Palm Oil Increases β-Carotene and Vitamin A Blood Levels in Patients with Cystic Fibrosis

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