Simon Y. Graeber

Berlin, BE, Germany

Last Updated: 09/26/2026

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Found 88 publications

Longitudinal Changes in Lung Morphologic Features and Perfusion Detected by MRI in Patients With Primary Ciliary Dyskinesia From Infancy Through Adulthood.

Longitudinal Changes in Lung Morphologic Features and Perfusion Detected by MRI in Patients With Primary Ciliary Dyskinesia From Infancy Through Adulthood.

Journal: Chest

Published: January 21, 2026

Chemical Synthesis of Pseudomonas aeruginosa, Staphylococcus aureus, and Acinetobacter baumannii Capsular Polysaccharide Fragments as Leads for Cross-Protection.

Chemical Synthesis of Pseudomonas aeruginosa, Staphylococcus aureus, and Acinetobacter baumannii Capsular Polysaccharide Fragments as Leads for Cross-Protection.

Journal: Angewandte Chemie (International ed. in English)

Published: November 03, 2025

Reflection confocal microscopy for quantitative assessment of airway surface layer dysregulation and pharmacological rescue in cystic fibrosis under near-physiological conditions.

Reflection confocal microscopy for quantitative assessment of airway surface layer dysregulation and pharmacological rescue in cystic fibrosis under near-physiological conditions.

Journal: Scientific reports

Published: September 17, 2025

The role of sweat chloride in determining CFTR protein restoration in people with cystic fibrosis.

The role of sweat chloride in determining CFTR protein restoration in people with cystic fibrosis.

Journal: The Lancet. Respiratory medicine

Published: August 29, 2025

Automated scoring of airway abnormalities and mucus plugging in chest magnetic resonance imaging of cystic fibrosis using artificial intelligence.

Automated scoring of airway abnormalities and mucus plugging in chest magnetic resonance imaging of cystic fibrosis using artificial intelligence.

Journal: Computational and structural biotechnology journal

Published: July 29, 2025

Breaking boundaries or a small piece of the puzzle: can CFTR modulators transform bronchiectasis care?

Breaking boundaries or a small piece of the puzzle: can CFTR modulators transform bronchiectasis care?

Journal: ERJ open research

Published: May 14, 2025

Changes in Sputum Viscoelastic Properties and Airway Inflammation in Primary Ciliary Dyskinesia are Comparable to Cystic Fibrosis on Elexacaftor/Tezacaftor/Ivacaftor Therapy.

Changes in Sputum Viscoelastic Properties and Airway Inflammation in Primary Ciliary Dyskinesia are Comparable to Cystic Fibrosis on Elexacaftor/Tezacaftor/Ivacaftor Therapy.

Journal: The European respiratory journal

Published: March 28, 2025

Identification and Characterization of a Rare Exon 22 Duplication in CFTR in Two Families.

Identification and Characterization of a Rare Exon 22 Duplication in CFTR in Two Families.

Journal: International journal of molecular sciences

Published: March 14, 2025

Reduction of systemic inflammation by elexacaftor/tezacaftor/ivacaftor correlates with lung function improvement in cystic fibrosis.

Reduction of systemic inflammation by elexacaftor/tezacaftor/ivacaftor correlates with lung function improvement in cystic fibrosis.

Journal: The European respiratory journal

Published: January 23, 2025

Perinatal dysfunction of innate immunity in cystic fibrosis.

Perinatal dysfunction of innate immunity in cystic fibrosis.

Journal: Science translational medicine

Published: January 22, 2025

Progress of personalized medicine of cystic fibrosis in the times of efficient CFTR modulators.

Progress of personalized medicine of cystic fibrosis in the times of efficient CFTR modulators.

Journal: Molecular and cellular pediatrics

Published: January 20, 2025

Quantitative MRI detects delayed perfusion and impact of bronchial artery dilatation on pulmonary circulation in patients with cystic fibrosis.

Quantitative MRI detects delayed perfusion and impact of bronchial artery dilatation on pulmonary circulation in patients with cystic fibrosis.

Journal: European radiology

Published: December 03, 2024

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Last Updated: 09/26/2026